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14 pages, 2186 KiB  
Article
Threonine Phosphorylation and the Yin and Yang of STAT1: Phosphorylation-Dependent Spectrum of STAT1 Functionality in Inflammatory Contexts
by Maha M. Elbrashy, Hozaifa Metwally, Shuhei Sakakibara and Tadamitsu Kishimoto
Cells 2024, 13(18), 1531; https://doi.org/10.3390/cells13181531 - 12 Sep 2024
Viewed by 223
Abstract
Threonine phosphorylation promotes inflammatory functions of STAT1 while restricting its interferon (IFN) signaling in innate immune responses. However, it remains unclear whether the restriction of STAT1-mediated IFN signaling conferred by threonine phosphorylation is a ubiquitous mechanism or one that is context-dependent. To address [...] Read more.
Threonine phosphorylation promotes inflammatory functions of STAT1 while restricting its interferon (IFN) signaling in innate immune responses. However, it remains unclear whether the restriction of STAT1-mediated IFN signaling conferred by threonine phosphorylation is a ubiquitous mechanism or one that is context-dependent. To address this, we utilized pristane-induced lupus, a prototype IFN-driven systemic autoimmune disease model characterized by the production of high-titer autoantibodies against nucleic acid-associated antigens. Through genetic and biochemical assays, we demonstrate that Thr748 phosphorylation is dispensable for STAT1 functionality in pristane-induced lupus. Genetically engineered mice expressing the phospho-deficient threonine 748-to-alanine (T748A) mutant STAT1 exhibited similar survival rates, high titers of anti-dsDNA IgG, and nephritis compared to their wild-type littermates. In sharp contrast, STAT1 deficiency protected mice against pristane-induced lupus, as evidenced by increased survival, low titers of anti-dsDNA IgG, and less severe nephritis in the STAT1 knockout mice compared to their T748A littermates. Our study suggests a phosphorylation-dependent modularity that governs the spectrum of STAT1 functionality in inflammatory contexts: IFN phospho-tyrosine-dependent and inflammatory phospho-threonine-dependent, with Thr748 phosphorylation driving selective inflammatory activities, particularly those not driven by the canonical JAK pathway. From a broader perspective, our findings provide deeper insights into how distinct phosphorylation events shape the combinatorial logic of signaling cassettes, thereby regulating context-dependent responses. Full article
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Figure 1

Figure 1
<p>T748A mice exhibited similar survival rates and high titers of autoantibodies compared to their Wt littermates following pristane-induced lupus. (<b>A</b>) Schematic diagram of experimental design; (<b>B</b>) survival rate of pristane-injected Wt and T748A littermates (<span class="html-italic">n</span> = 16 mice per genotype); (<b>C</b>,<b>D</b>) serum levels of anti-dsDNA IgG of naïve and pristane-injected Wt and T748A littermates as measured by ELISA (<span class="html-italic">n</span> = 8 mice per genotype per group). <span class="html-italic">p</span> values are shown as measured by log-rank test (Mantel-Cox) (<b>B</b>), one-way ANOVA with post hoc Tukey’s test (<b>C</b>), or unpaired student’s <span class="html-italic">t</span> test with Welch’s correction (<b>D</b>). NT, non-treated.</p>
Full article ">Figure 2
<p>Thr748 phosphorylation is dispensable for Stat1-mediated cytokines expression and IFN signaling following pristane-induced lupus. (<b>A</b>–<b>G</b>) Splenocytes from pristane-injected Wt and T748A littermates. Total RNA was isolated, and the indicated transcripts were quantified by qRT PCR. Data are presented as medians (<span class="html-italic">n</span> = 3 biological replicates). (<b>H</b>) Splenocytes from naïve and pristane-injected Wt and T748A littermates. Whole-cell lysates were harvested and separated by SDS PAGE. The indicated endogenous proteins were detected by Western blotting analysis. Data show three independent biological replicates per genotype per group. (<b>I</b>) Quantification of mean band intensities of (<b>H</b>). <span class="html-italic">p</span> values are shown as measured by unpaired student’s <span class="html-italic">t</span> test with Welch’s correction (<b>A</b>–<b>G</b>) and one-way ANOVA with post hoc Tukey’s test (<b>I</b>). NT, non-treated.</p>
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<p>T748A mice exhibited similar albuminuria and glomerulonephritis compared to their Wt littermates following pristane-induced lupus. (<b>A</b>) Measurements of the levels of albumin/creatinine in the urine of pristane-injected Wt and T748A littermates as measured by ELISA. (<b>B</b>) Histopathological analysis of glomerulonephritis. Scale bar, 100 μm. (<b>C</b>) Immunofluorescent analysis of autoantibodies deposition in glomeruli. Scale bar, 50 μm. Data are representative of two independent experiments. <span class="html-italic">n</span> = 8 mice per genotype per group for each experiment. <span class="html-italic">p</span> values are shown as measured by unpaired student’s <span class="html-italic">t</span> test with Welch’s correction (<b>A</b>). NT, non-treated.</p>
Full article ">Figure 4
<p>Thr748 phosphorylation is dispensable for STAT1-mediated pathology in pristane-induced lupus. (<b>A</b>) Survival rate of pristane-injected KO and T748A littermates. (<b>B</b>,<b>C</b>) Serum levels of anti-dsDNA IgG of naïve and pristane-injected KO and T748A littermates as measured by ELISA. (<b>D</b>) Measurements of the levels of albumin/creatinine in urine of pristane-injected KO and T748A littermates as measured by ELISA. (<b>E</b>) Histopathological analysis of glomerulonephritis. Data are representative of two independent experiments. <span class="html-italic">n</span> = 4–8 mice per genotype per group for each experiment. Scale bar, 100 μm. <span class="html-italic">p</span> values are shown as measured by log-rank test (Mantel-Cox) (<b>A</b>), one-way ANOVA with post hoc Tukey’s test (<b>B</b>), or unpaired student’s <span class="html-italic">t</span> test with Welch’s correction (<b>C</b>,<b>D</b>). NT, non-treated.</p>
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<p>Scheme for a phosphorylation-dependent spectrum of STAT1 functionality in inflammatory contexts: IFN phospho-tyrosine-dependent and inflammatory phospho-threonine-dependent.</p>
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16 pages, 5246 KiB  
Article
Joint Inflammation Correlates with Joint GPR30 Expression in Males and Hippocampal GPR30 Expression in Females in a Rat Model of Rheumatoid Arthritis
by Tanja Grubić Kezele, Hrvoje Omrčen, Lara Batičić, Sandra Šućurović and Sanja Zoričić Cvek
Int. J. Mol. Sci. 2024, 25(14), 7864; https://doi.org/10.3390/ijms25147864 - 18 Jul 2024
Viewed by 1092
Abstract
It is not entirely clear how the interaction between joint inflammation and the central nervous system (CNS) response in rheumatoid arthritis (RA) works, and what pathophysiology underlies the sex differences in coexisting neuropsychiatric comorbidities. It is known that estrogen hormones reduce inflammation in [...] Read more.
It is not entirely clear how the interaction between joint inflammation and the central nervous system (CNS) response in rheumatoid arthritis (RA) works, and what pathophysiology underlies the sex differences in coexisting neuropsychiatric comorbidities. It is known that estrogen hormones reduce inflammation in RA and that this occurs mainly via the stimulation of G protein-coupled receptor-30 (GPR30), also known as G protein-coupled estrogen receptor (GPER) 1. However, changes in GPR30 expression and sex differences induced by local and systemic inflammation in RA are not yet known. Our aim was to reveal sex differences in the expression and association of joint GPR30 with local and systemic inflammation, clinical course and furthermore with hippocampal GPR30 expression during pristane-induced arthritis (PIA) in Dark Agouti (DA) rats, an animal model of RA. Furthermore, we demonstrated sex-specific differences in the association between joint and systemic inflammation and hippocampal microglia during PIA. Our results suggest sex-specific differences not only in the clinical course and serum levels of pro-inflammatory cytokines but also in the expression of GPR30. Female rats show greater synovial inflammation and greater damage to the articular cartilage compared to males during PIA attack. Male rats express higher levels of synovial and cartilaginous GPR30 than females during PIA, which correlates with a less severe clinical course. The correlation between synovial and cartilaginous GPR30 and joint inflammation scores (Krenn and Mankin) in male rats suggests that the more severe the joint inflammation, the higher the GPR30 expression. At the same time, there is no particular upregulation of hippocampal GPR30 in males. On the other hand, female rats express higher levels of neuroprotective GPR30 in the hippocampus than male rats at the basic level and during PIA attack. In addition, females have a higher number of Iba-1+ cells in the hippocampus during PIA attack that strongly correlates with the clinical score, serum levels of IL-17A, and Krenn and Mankin scores. These results suggest that male rats are better protected from inflammation in the joints and female rats are better protected from the inflammation in the hippocampus during a PIA attack, independently of microglia proliferation. However, in the remission phase, synovial GPR30 expression suddenly increases in female rats, as does hippocampal GPR30 expression in males. Further experiments with a longer remission period are needed to investigate the molecular background of these sex differences, as well as microglia phenotype profiling. Full article
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Figure 1
<p>Clinical course. The clinical course in the male (n = 45) and female (n = 45) rat groups. Values are presented as mean ± SD using PIA scores of each animal for every day. Mann–Whitney U test revealed no statistical significance (<span class="html-italic">p</span> = 0.847).</p>
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<p>Pristane-induced arthritis upregulates synovial GPR30 expression mostly in male DA rats, which is in strong positive correlation with clinical and Krenn synovitis score. (<b>A</b>) Representative immunofluorescent and immunohistological pictures show staining with anti-GPR30 antibodies in paraffin-embedded sections of metatarsophalangeal joints (synovial tissue) obtained from male and female DA rats: control (treated with saline); PIA onset (between 9th and 12th day after induction); PIA peak (between 16th and 20th day after induction); PIA remission (between 20th and 25th day after induction). Scale bars indicate 50 μm. (<b>B</b>) Quantification of synovial GPR30 expression was performed using Cell F v3.1 software analysis on 12 regions of interest (3 slides/rat × 6 rats/group = 18 slides/group and total 24 rats). Values are expressed as mean value ± SE. One-way ANOVA followed by the post hoc Scheffé test: * difference between male and female rats; <sup>X</sup> difference between male control and male PIA rats; # difference between female control and female PIA rats; <sup>XXX</sup> <span class="html-italic">p</span> &lt; 0.001; ### <span class="html-italic">p</span> &lt; 0.001; *** <span class="html-italic">p</span> &lt; 0.001. (<b>C</b>) Pearson’s correlation between expression of synovial GPR30 and Krenn synovitis score, clinical score and serum level of IL-17A and TNF: ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Pristane-induced arthritis upregulates cartilage GPR30 expression mostly in male DA rats, which is in strong positive correlation with clinical and Mankin synovitis score. (<b>A</b>) Representative immunofluorescent and immunohistological pictures show staining with anti-GPR30 antibodies in paraffin-embedded sections of metatarsophalangeal joints (cartilage) obtained from male and female DA rats: control (treated with saline); PIA onset (between 9th and 12th day after induction); PIA peak (between 16th and 20th day after induction); PIA remission (between 20th and 25th day after induction). Insert show staining in slides incubated without primary anti-GPR30 antibodies (negative control). Scale bars indicate 50 μm. (<b>B</b>) Quantification of cartilaginous GPR30 expression was performed using Cell F v3.1 software analysis on 12 regions of interest (3 slides/rat × 6 rats/group = 18 slides/group and total 24 rats). Values are expressed as mean value ± SE. One-way ANOVA followed by the post hoc Scheffé test: * difference between male and female rats; <sup>X</sup> difference between male control and male PIA rats; # difference between female control and female PIA rats; <sup>XXX</sup> <span class="html-italic">p</span> &lt; 0.001; ### <span class="html-italic">p</span> &lt; 0.001; *** <span class="html-italic">p</span> &lt; 0.001. (<b>C</b>) Pearson’s correlation between expression of cartilage GPR30 and Mankin synovitis score, clinical score, and serum level of IL-17A and TNF: *** <span class="html-italic">p</span> &lt; 0.001.</p>
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<p>Pristane-induced arthritis upregulates hippocampal GPR30 expression in the acute phase but downregulates in the remission phase of female rats, which is in strong negative correlation with the serum level of TNF. (<b>A</b>) Representative immunofluorescent pictures show staining with anti-GPR30 antibodies in paraffin-embedded sections of brain tissue (hippocampus/DG) obtained from male and female DA rats: control (treated with saline); PIA onset (between 9th and 12th day after induction); PIA peak (between 16th and 20th day after induction); PIA remission (between 20th and 25th day after induction). Scale bars indicate 50 μm. (<b>B</b>) Quantification of hippocampal GPR30 expression was performed using Cell F v3.1 software analysis on 12 regions of interest (three slides/rat × six rats/group = 18 slides/group and total 24 rats). Values are expressed as mean value ± SE. One-way ANOVA followed by the post hoc Scheffé test: * difference between male and female rats; <sup>X</sup> difference between male control and male PIA rats; # difference between female control and female experiment rats; <sup>XXX</sup> <span class="html-italic">p</span> &lt; 0.001; ### <span class="html-italic">p</span> &lt; 0.001; *** <span class="html-italic">p</span> &lt; 0.001. (<b>C</b>) Pearson’s correlation between hippocampal GPR30 expression, clinical score, serum level of IL-17A and TNF, Krenn synovitis and Mankin osteoarthritis score: ** <span class="html-italic">p</span> &lt; 0.01.</p>
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<p>Pristane-induced arthritis upregulates the number of hippocampal Iba-1+ cells mostly in female DA rats, which is in positive correlation with the clinical score, serum level of IL-17A and the Krenn synovitis and Mankin osteoarthritis scores. (<b>A</b>) Representative immunofluorescent pictures show staining with anti-Iba-1 antibody in paraffin-embedded sections of brain tissue (hippocampus/DG) obtained from male and female DA rats: control (treated with saline); PIA onset (between 9th and 12th day after induction); PIA peak (between 16th and 20th day after induction); PIA remission (between 20th and 25th day after induction). Scale bars indicate 50 μm. (<b>B</b>) The number of hippocampal Iba-1+ cells per mm<sup>2</sup>. Cells were manually counted in regions of interest (12 ROI/4 μm slide x 3 slides/rat × 6 rats/group = 18 slides/group and total 24 rats). Values are expressed as mean value ± SE. One-way ANOVA followed by the post hoc Scheffé test: * difference bewteen male and female rats; <sup>X</sup> difference between male control and male experiment rats; # difference between female control and female PIA rats; <sup>X</sup> <span class="html-italic">p</span> &lt; 0.05, ### <span class="html-italic">p</span> &lt; 0.001; and *** <span class="html-italic">p</span> &lt; 0.001. (<b>C</b>) Pearson’s correlation between the number of hippocampal Iba-1+ cells, hippocampal GPR30 expression, clinical score, serum level of IL-17A and TNF, Krenn synovitis and Mankin osteoathritis score: * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001.</p>
Full article ">Figure 6
<p>Disease scoring system. The maximum score per limb and rat was 15 and 60, respectively. Scores were not given for deformations if they were not accompanied by erythema or swelling. (<b>A</b>) Normal hind paw without the inflammation. (<b>B</b>) Inflammed and swolen ankle of a hind paw after PIA induction. (<b>C</b>) Illustration of a hind paw from the dorsal side with score points. (<b>D</b>) Illustration of a front paw from the dorsal side with score points. (<b>E</b>) Illustration of a hind paw from the medial side with score points.</p>
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<p>Rat hippocampus from the medial side. DG, dentate gyrus, CA, <span class="html-italic">cornu Ammonis</span>. Magnification 40×.</p>
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16 pages, 2494 KiB  
Article
Bacterial Diversity in Old Hydrocarbon Polluted Sediments of Ecuadorian Amazon River Basins
by Lara S. Corral-García, María Carmen Molina, Luis Fernando Bautista, Raquel Simarro, Carlos Iván Espinosa, Guillermo Gorines-Cordero and Natalia González-Benítez
Toxics 2024, 12(2), 119; https://doi.org/10.3390/toxics12020119 - 31 Jan 2024
Viewed by 1597
Abstract
The Ecuadorian Amazon rainforest stands out as one of the world’s most biodiverse regions, yet faces significant threats due to oil extraction activities dating back to the 1970s in the northeastern provinces. This research investigates the environmental and societal consequences of prolonged petroleum [...] Read more.
The Ecuadorian Amazon rainforest stands out as one of the world’s most biodiverse regions, yet faces significant threats due to oil extraction activities dating back to the 1970s in the northeastern provinces. This research investigates the environmental and societal consequences of prolonged petroleum exploitation and oil spills in Ecuador’s Amazon. Conducted in June 2015, the study involved a comprehensive analysis of freshwater sediment samples from 24 locations in the Rio Aguarico and Napo basins. Parameters such as water and air temperature, conductivity, soil pH, and hydrocarbon concentrations were examined. Total petroleum hydrocarbon (TPH) concentrations ranged from 9.4 to 847.4 mg kg−1, with polycyclic aromatic hydrocarbon (PAH) levels varying from 10.15 to 711.1 mg kg−1. The pristane/phytane ratio indicated historic hydrocarbon pollution in 8 of the 15 chemically analyzed sediments. Using non-culturable techniques (Illumina), bacterial analyses identified over 350 ASV, with prominent families including Comamonadaceae, Chitinophagaceae, Anaeromyxobacteraceae, Sphingomonadaceae, and Xanthobacteraceae. Bacterial diversity, assessed in eight samples, exhibited a positive correlation with PAH concentrations. The study provides insights into how microbial communities respond to varying levels of hydrocarbon pollution, shedding light on the enduring impact of oil exploitation in the Amazonian region. Its objective is to deepen our understanding of the environmental and human well-being in the affected area, underscoring the pressing need for remedial actions in the face of ongoing ecological challenges. Full article
(This article belongs to the Section Ecotoxicology)
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<p>Study area with the sampled locations (red circles) and the crude oil well Aguarico 4 (black circle).</p>
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<p>Pristane/phytane (Pr/Ph) ratio and the total petroleum hydrocarbon (TPH) concentrations (mg kg<sup>−1</sup>) at the different sampled points. The dashed line represents the fact that the Pr/Ph ratio is equal to 1.</p>
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<p>Microbial diversity (ASVs) at a family level (12 most abundant families) in each sediment sample (left axis) and the polycyclic aromatic hydrocarbon concentrations (PAH, mg·kg<sup>−1</sup>) in each sample (right axis).</p>
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<p>Linear relationship between the diversity Shannon–Wiener Index (H) and the polycyclic aromatic hydrocarbon (PAH, mg kg<sup>−1</sup>) concentrations in each sediment sample.</p>
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19 pages, 3023 KiB  
Article
Analysis of Kazakhstan Crude Oil Biomarkers by Gas Chromatography in Combination with Mass Spectrometry
by Mereke Alimzhanova and Bauyrzhan Abdykarimov
Separations 2023, 10(11), 561; https://doi.org/10.3390/separations10110561 - 9 Nov 2023
Cited by 1 | Viewed by 2332
Abstract
Kazakhstan ranks as the 12th largest oil producer globally and boasts a diverse range of crude oils. This research introduces a method for distinguishing between the different types of crude oils based on biomarker analysis of 28 crude oils from Western and Southern [...] Read more.
Kazakhstan ranks as the 12th largest oil producer globally and boasts a diverse range of crude oils. This research introduces a method for distinguishing between the different types of crude oils based on biomarker analysis of 28 crude oils from Western and Southern Kazakhstan using gas chromatography-mass spectrometry. Biomarkers serve as valuable tools, especially in forensic investigations of oil spills. These biomarkers effectively retain a significant portion of the original natural product’s carbon structure, providing crucial evidence regarding the origin and identity of the oils under examination. This study identifies a set of biomarkers, including pristine, phytane, n-C17 and n-C18 alkanes, hopanes, bisnorhopanes, iso-copalanes, pregnane, androstane, allopregnane, homopregnane, cholestane, and stigmastane. By examining ratios such as pristane/phytane, pristane/n-C17 alkane, tricyclic/pentacyclic terpanes, and hopane, as well as the distribution of steranes, it was deduced that crude oils from West Kazakhstan exhibited resilience to biodegradation. These findings showed that gas chromatography-mass spectrometry is an effective method for oil biomarkers determination, especially because it provides efficient separation and identification. Additionally, this study delved into the origin conditions and maturity of these oils, contributing to a deeper understanding of their characteristics and analysis that is simple to use and available worldwide. Full article
(This article belongs to the Topic Oil, Gas and Water Separation Research)
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Figure 1
<p>Total peak area of terpanes of the function of injection temperature (<b>A</b>) and oven temperature program (<b>B</b>).</p>
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<p>Molecular chemical structures for the biomarkers.</p>
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<p>Oxidation and reduction reaction of phytol.</p>
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<p>Chromatograms of Nuraly (<b>A</b>) and Kosshagyl (<b>B</b>) crude oils at <span class="html-italic">m/z</span> 57.</p>
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<p>Plot of Pr/n-C<sub>17</sub> vs. Ph/n-C<sub>18</sub> showing the sources from the West Kazakhstan crude oils.</p>
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<p>Plot of Pr/n-C<sub>17</sub> vs. Ph/n-C<sub>18</sub> showing the sources from the South Kazakhstan crude oils.</p>
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<p>C<sub>27</sub> and C<sub>29</sub> Steranes (<span class="html-italic">m/z</span> 217) distribution of West Kazakhstan crude oils (numbering according to the <a href="#separations-10-00561-t001" class="html-table">Table 1</a>).</p>
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<p>C<sub>27</sub> and C<sub>29</sub> Steranes (<span class="html-italic">m/z</span> 217) distribution of South Kazakhstan crude oils (numbering according to the <a href="#separations-10-00561-t001" class="html-table">Table 1</a>).</p>
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<p>Distribution of ratio tricyclic/pentacyclic terpanes as maturity indicator for West (<b>A</b>) and South (<b>B</b>) Kazakhstan crude oils (numbering according to the <a href="#separations-10-00561-t001" class="html-table">Table 1</a>).</p>
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21 pages, 4154 KiB  
Article
Characterization of the Mycoremediation of n-Alkanes and Branched-Chain Alkanes by Filamentous Fungi from Oil-Polluted Soil Samples in Kazakhstan
by Mariam Gaid, Doreen Pöpke, Anne Reinhard, Ramza Berzhanova, Togzhan Mukasheva, Tim Urich and Annett Mikolasch
Microorganisms 2023, 11(9), 2195; https://doi.org/10.3390/microorganisms11092195 - 30 Aug 2023
Cited by 1 | Viewed by 1100
Abstract
For decades, researchers have focused on containing terrestrial oil pollution. The heterogeneity of soils, with immense microbial diversity, inspires them to transform pollutants and find cost-effective bioremediation methods. In this study, the mycoremediation potentials of five filamentous fungi isolated from polluted soils in [...] Read more.
For decades, researchers have focused on containing terrestrial oil pollution. The heterogeneity of soils, with immense microbial diversity, inspires them to transform pollutants and find cost-effective bioremediation methods. In this study, the mycoremediation potentials of five filamentous fungi isolated from polluted soils in Kazakhstan were investigated for their degradability of n-alkanes and branched-chain alkanes as sole carbon and energy sources. Dry weight estimation and gas chromatography–mass spectrometry (GC-MS) monitored the growth and the changes in the metabolic profile during degradation, respectively. Penicillium javanicum SBUG-M1741 and SBUG-M1742 oxidized medium-chain alkanes almost completely through mono- and di-terminal degradation. Pristane degradation by P. javanicum SBUG-M1741 was >95%, while its degradation with Purpureocillium lilacinum SBUG-M1751 was >90%. P. lilacinum SBUG-M1751 also exhibited the visible degradation potential of tetradecane and phytane, whereby in the transformation of phytane, both the mono- and di-terminal degradation pathways as well as α- and ß-oxidation steps could be described. Scedosporium boydii SBUG-M1749 used both mono- and di-terminal degradation pathways for n-alkanes, but with poor growth. Degradation of pristane by Fusarium oxysporum SBUG-M1747 followed the di-terminal oxidation mechanism, resulting in one dicarboxylic acid. These findings highlight the role of filamentous fungi in containing oil pollution and suggest possible degradation pathways. Full article
(This article belongs to the Section Environmental Microbiology)
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Figure 1
<p>Growth of <span class="html-italic">P. javanicum</span> strains on tetradecane or pristane as the sole carbon and energy source and the remaining substrate after 7 days of incubation. (<b>a</b>) SBUG-M1741 with 0.5% tetradecane, (<b>b</b>) SBUG-M1742 with 0.5% tetradecane, and (<b>c</b>) SBUG-M1741 with 0.1% pristane.</p>
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<p>Growth of <span class="html-italic">S. boydii</span> SBUG-M1749 and the remained substrate after 7-day incubation with 0.5% tetradecane as the sole carbon and energy source.</p>
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<p>Growth of <span class="html-italic">F. oxysporum</span> SBUG-M1747 and the remaining substrate after 7-day incubation with 0.1% pristane as the sole carbon and energy source.</p>
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<p>Growth of <span class="html-italic">P. lilacinum</span> SBUG-M1751 on tetradecane, pristane, or phytane as the sole carbon and energy source and the remaining substrates after 7 days of incubation. (<b>a</b>) 0.25% tetradecane, (<b>b</b>) 0.1% pristane, and (<b>c</b>) 0.01% phytane.</p>
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<p>Degradation scheme of the carboxylic acids after methylation presenting mono- and di-terminal oxidations of tetradecane by <span class="html-italic">Penicillium javanicum</span> SBUG-M1741 and SBUG-M1742, <span class="html-italic">Scedosporium boydii</span> SBUG-M1749, and <span class="html-italic">Purpureocillium lilacinum</span> SBUG-M1751. Structures that were not detected in the current study are marked by brackets. Pn refers to the product number as per its appearance in <a href="#microorganisms-11-02195-t002" class="html-table">Table 2</a>.</p>
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<p>Degradation scheme of the carboxylic acids after methylation presenting mono- and di-terminal oxidations of pristane by <span class="html-italic">Penicillium javanicum</span> SBUG-M1741, <span class="html-italic">Fusarium oxysporum</span> SBUG-M1747, and <span class="html-italic">Purpureocillium lilacinum</span> SBUG-M1751 [<a href="#B51-microorganisms-11-02195" class="html-bibr">51</a>,<a href="#B56-microorganisms-11-02195" class="html-bibr">56</a>]. Structures that were not detected in the current study are marked by brackets. Pn refers to the product number as per its appearance in <a href="#microorganisms-11-02195-t003" class="html-table">Table 3</a>.</p>
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<p>Degradation scheme of the carboxylic acids after methylation presenting mono- and di-terminal oxidations of phytane by <span class="html-italic">Purpureocillium lilacinum</span> SBUG-M1751. The α-oxidation is adapted according to previously published data [<a href="#B51-microorganisms-11-02195" class="html-bibr">51</a>,<a href="#B52-microorganisms-11-02195" class="html-bibr">52</a>,<a href="#B58-microorganisms-11-02195" class="html-bibr">58</a>]. Structures that were not detected in the current study are marked by brackets. Pn refers to the product number as per its appearance in <a href="#microorganisms-11-02195-t004" class="html-table">Table 4</a>.</p>
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18 pages, 3613 KiB  
Article
Organic Geochemistry of Crude Oils from the Kohat Basin, Pakistan
by Syed Mamoon Siyar, Fayaz Ali, Sajjad Ahmad, George Kontakiotis, Hammad Tariq Janjuhah, Samina Jahandad and Waqas Naseem
Geosciences 2023, 13(7), 199; https://doi.org/10.3390/geosciences13070199 - 29 Jun 2023
Cited by 2 | Viewed by 1742
Abstract
The crude oils from the reservoirs of Mela-01 and Mela-04 wells located in the Kohat Basin, Pakistan, were geochemically analyzed to evaluate the origin, depositional conditions, and thermal maturity of the rock units and possible facies from which these oils were sourced. Gas [...] Read more.
The crude oils from the reservoirs of Mela-01 and Mela-04 wells located in the Kohat Basin, Pakistan, were geochemically analyzed to evaluate the origin, depositional conditions, and thermal maturity of the rock units and possible facies from which these oils were sourced. Gas chromatography-mass spectrometry (GC-MS) was performed on the samples to obtain biomarker and non-biomarker parameters. Analyzed non-biomarker parameters, including carbon preference index (CPI), terrigenous to aquatic ratio (TAR), isoprenoids pristane to phytane (Pr/Ph), and biomarker parameters, including steranes and dibenzothiophene/phenanthrene (DBT/P) of aromatic compounds, were utilized in the present study to achieve the objectives. Most of these parameters suggest a mixed source of organic matter (marine/terrestrial) with sub-oxic conditions in the source rocks for the analyzed oil samples in the studied wells from Mela oilfield, Kohat Basin. Furthermore, the CPI and different biomarker parameters such as steranes C29 S/S + R, ββ/αα + ββ), moretane to hopane (M29/C30H), pentacyclic terpanes C27 (Ts/Ts + Tm), H32 (S/S + R) hopanes, and aromatic methylphenanthrene index (MPI) indicate that the analyzed oils have originated from thermally mature rocks falling in the oil window. As the studied Kohat Basin has multiple source rocks and contributes to the major petroleum production of the country, the present investigations reveal that its okthe Mela oils were generated by the strata of mixed organic matter that were deposited in marine sub-oxic conditions. Furthermore, this study suggests that this stratum would also have been produced in unexplored surrounding areas such as Tirah, Orakzai, and the Bannu Depression. Full article
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<p>Tectonic map illustrating structural elements of the northern Pakistan and showing the location of the study area. The blue lines indicate the river flow, while the black triangles corresponds to thrusting, and red lines to thrust faults, respectively (modified by [<a href="#B46-geosciences-13-00199" class="html-bibr">46</a>]).</p>
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<p><span class="html-italic">m</span>/<span class="html-italic">z</span> 57 chromatograms representing n-alkanes and isoprenoids in Mela oils in the study area. (<b>a</b>) Mela-01, and (<b>b</b>) Mela-04 wells, respectively.</p>
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<p>(<b>a</b>,<b>b</b>) Chromatograms showing distribution of C<sub>27</sub>, C<sub>28</sub>, and C<sub>29</sub> steranes in the studied Mela oils from Kohat Basin.</p>
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<p>(<b>a</b>,<b>b</b>) Terpanes (<span class="html-italic">m</span>/<span class="html-italic">z</span> 19) distribution in the analyzed oils from Mela oilfield.</p>
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<p>Aromatic hydrocarbon (<span class="html-italic">m</span>/<span class="html-italic">z</span> 178, 184 and 192) in the analyzed oils from Mela oilfield in the study area. (<b>a</b>) Mela-01, and (<b>b</b>) Mela-04 wells, respectively.</p>
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<p>Organic source and redox conditions of the examined oils in the studied wells through the (<b>a</b>) Pr/n-C<sub>17</sub> vs. Ph/nC<sub>18</sub> and (<b>b</b>) Pr/Ph vs. CPI cross plots.</p>
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<p>Organic source and redox conditions of the examined oils in the studied wells through the (<b>a</b>) Pr/n-C<sub>17</sub> vs. Ph/nC<sub>18</sub> and (<b>b</b>) Pr/Ph vs. CPI cross plots.</p>
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<p>Ternary plot of regular steranes (C<sub>27</sub>–C<sub>29</sub>) of the analyzed oils from Mela oilfield indicating source of organic matter in the study area.</p>
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<p>Facies analysis for the analyzed crude oils in Mela oilfield using (<b>a</b>) C<sub>35</sub>/C<sub>34</sub> hopane vs. C<sub>29</sub>/C<sub>30</sub> H plot, (<b>b</b>) Ts/Tm vs. C<sub>35</sub>/C<sub>34</sub> H plot, and (<b>c</b>) DBT/P and Pr/Ph cross plot.</p>
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<p>Biomarker’s parameters showing maturity of the analyzed oil samples from the study area using (<b>a</b>) C<sub>29</sub> ββ/αα + ββ) vs. C<sub>32</sub> 22S/(22S + 22R) plot, and (<b>b</b>) C<sub>29</sub> ββ/αα + ββ) vs. C<sub>29</sub> (S/S + R) plot. The circle indicates the area of the marine shale lithology of the analyzed oils.</p>
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23 pages, 4966 KiB  
Article
Effects of Dietary Oleacein Treatment on Endothelial Dysfunction and Lupus Nephritis in Balb/C Pristane-Induced Mice
by Rocío Muñoz-García, Marina Sánchez-Hidalgo, Manuel Alcarranza, María Victoria Vazquéz-Román, María Alvarez de Sotomayor, María Luisa González-Rodríguez, María C. de Andrés and Catalina Alarcón-de-la-Lastra
Antioxidants 2023, 12(6), 1303; https://doi.org/10.3390/antiox12061303 - 19 Jun 2023
Cited by 1 | Viewed by 1889
Abstract
Systemic lupus erythematosus (SLE) is a chronic immune-inflammatory disease characterized by multiorgan affectation and lowered self-tolerance. Additionally, epigenetic changes have been described as playing a pivotal role in SLE. This work aims to assess the effects of oleacein (OLA), one of the main [...] Read more.
Systemic lupus erythematosus (SLE) is a chronic immune-inflammatory disease characterized by multiorgan affectation and lowered self-tolerance. Additionally, epigenetic changes have been described as playing a pivotal role in SLE. This work aims to assess the effects of oleacein (OLA), one of the main extra virgin olive oil secoiridoids, when used to supplement the diet of a murine pristane-induced SLE model. In the study, 12-week-old female BALB/c mice were injected with pristane and fed with an OLA-enriched diet (0.01 % (w/w)) for 24 weeks. The presence of immune complexes was evaluated by immunohistochemistry and immunofluorescence. Endothelial dysfunction was studied in thoracic aortas. Signaling pathways and oxidative-inflammatory-related mediators were evaluated by Western blotting. Moreover, we studied epigenetic changes such as DNA methyltransferase (DNMT-1) and micro(mi)RNAs expression in renal tissue. Nutritional treatment with OLA reduced the deposition of immune complexes, ameliorating kidney damage. These protective effects could be related to the modulation of mitogen-activated protein kinases, the Janus kinase/signal transducer and transcription activator of transcription, nuclear factor kappa, nuclear-factor-erythroid-2-related factor 2, inflammasome signaling pathways, and the regulation of miRNAs (miRNA-126, miRNA-146a, miRNA-24-3p, and miRNA-123) and DNMT-1 expression. Moreover, the OLA-enriched diet normalized endothelial nitric oxide synthase and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase-1 overexpression. These preliminary results suggest that an OLA-supplemented diet could constitute a new alternative nutraceutical therapy in the management of SLE, supporting this compound as a novel epigenetic modulator of the immunoinflammatory response. Full article
(This article belongs to the Section Natural and Synthetic Antioxidants)
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<p>Immunomodulatory effect of an OLA-supplemented diet on the weight of the spleen and thymus organs 6 months after pristane induction. Data are expressed as the mean ± SEM (<span class="html-italic">n</span> = 10). One-way ANOVA followed by Tukey’s post hoc test results: ## <span class="html-italic">p</span> &lt; 0.01 vs. naïve control group; * <span class="html-italic">p</span> &lt; 0.05 vs. SD-pristane group.</p>
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<p>Histological effects of OLA dietary treatment on pristane-induced SLE mice. Representative images of (<b>A</b>–<b>C</b>) H&amp;E staining; (<b>D</b>–<b>F</b>) PAS, and (<b>G</b>–<b>I</b>) MT stains from renal tissues from mice. Normal histology architecture in the cortex and medullary renal naïve mice with low stroma between renal tubules (<b>A</b>,<b>G</b>) and normal glomeruli in the cortex parenchyma (<b>D</b>, arrows). Compressed glomeruli in SD-Pristane mice (<b>B</b>, arrows), probably due to Bowman space proliferation with the partial sclerosis of glomerular tufts. Inflammatory cells occupying the medullary interstitium (<b>E</b>, arrows). Fibrotic tissue characterized by an abundance of collagen along with hemorrhagic signs identified in the medullary stroma (<b>H</b>). OLA-treated mice showed no histopathological changes either in the medullary or renal cortex. Normal distribution of renal tubules in medullary parenchyma (<b>C</b>), two glomeruli showing regular size and shape (<b>F</b>, arrows), and a renal cortex with no fibrosis or pathologic changes (<b>I</b>). Scale bar, 25 µm (<b>A</b>–<b>I</b>). Scale bar, 100 µm (<b>H</b> black-dotted squared).</p>
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<p>An OLA-supplemented diet reduced IgG and IgM deposits in the kidney tissue of pristane-induced SLE mice. Representative figures of (<b>A</b>–<b>F</b>) IHC and (<b>G</b>–<b>L</b>) IF staining of IgG or IgM in kidneys from pristane-induced SLE mice. (<b>A</b>,<b>D</b>,<b>G</b>,<b>J</b>) Absence of deposits of IgG and IgM in the naïve group. (<b>B</b>,<b>E</b>,<b>H</b>,<b>K</b>) Marked IgG and IgM deposits in the renal glomeruli of SD-pristane mice. (<b>B</b>,<b>E</b>, black arrows) Deposits in the capillary loops and mesangial cells and into the tubular interstices (extraglomerular nephritis). Deposits in capillary loops (<b>H</b>, white arrow) and mesangial deposits (<b>H</b>, yellow arrow) (mesangio—capillary glomerulonephritis). They were also accompanied by extraglomerular deposits. Mesangial glomerulonephritis (<b>K</b>, yellow arrow) also appeared with intracapillary deposits (<b>K</b>, white arrow) and tubular involvement. Scale bar, 25 µm.</p>
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<p>Dietary OLA administration reduced COX-2, iNOS, and mPGES-1 protein overexpression. Protein expression was measured in total kidney homogenates from mice. Densitometry was performed after normalization to the control (β-actin housekeeping gene). One-way ANOVA followed by Tukey’s post hoc test results: ## <span class="html-italic">p</span> &lt; 0.01, ### <span class="html-italic">p</span> &lt; 0.001 vs. naïve group; ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 vs. SD-pristane group. Data were represented as the mean ± SEM (<span class="html-italic">n</span> = 6).</p>
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<p>Role of the OLA dietary treatment in the regulation of SLE-related intracellular signaling pathways. Protein expressions of (<b>A</b>) phosphorylated JAK3/STAT-3; (<b>B</b>) the Nrf-2/HO-1 axis; (<b>C</b>) the IκB-α and p65/p50 nuclear subunits, and (<b>D</b>) phosphorylated P38, JNK, and ERK MAPKs were evaluated in renal homogenates from mice. Densitometry was performed after normalization to the control (JNK, ERK, p38, or β-actin). Data are represented as the means ± SEM (<span class="html-italic">n</span> = 6). One-way ANOVA followed by Tukey’s post hoc test results: # <span class="html-italic">p</span> &lt; 0.05, ## <span class="html-italic">p</span> &lt; 0.01, ### <span class="html-italic">p</span> &lt; 0.001 vs. naïve group; * <span class="html-italic">p</span> &lt; 0.05, ** <span class="html-italic">p</span> &lt; 0.01, *** <span class="html-italic">p</span> &lt; 0.001 significant difference versus SD-pristane group.</p>
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<p>The inflammasome signaling pathway was downregulated by an OLA-supplemented diet. (<b>A</b>) NLRP3/ASC, (<b>B</b>) Caspase 11, (<b>C</b>) IL-18, and (<b>D</b>) Caspase 1. Protein expressions were analyzed by immunoblots in kidney lysates. Densitometry was performed following normalization to the control (β-actin housekeeping gene). Data are represented as the means ± SEM (<span class="html-italic">n</span> = 6). One-way analysis of variance (ANOVA), using Tukey–Kramer multiple comparisons test as post hoc test: # <span class="html-italic">p</span> &lt; 0.05, ## <span class="html-italic">p</span> &lt; 0.01, ### <span class="html-italic">p</span> &lt; 0.001 vs. naïve group; * <span class="html-italic">p</span> &lt; 0.05 ** <span class="html-italic">p</span> &lt; 0.01; significant difference versus SD-pristane group.</p>
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<p>The OLA-supplemented diet enhanced redox-sensitive effectors and endothelial function in pristane-induced mice. (<b>B</b>) NOX-1 and (<b>C</b>) penos Thr495 protein expression quantification in homogenates of aortic rings from mice. Data are represented as the mean ± SEM (<span class="html-italic">n</span> = 6). β-Actin was used as a loading control. One-way ANOVA followed by Tukey’s post hoc test results: # <span class="html-italic">p</span> &lt; 0.05, ### <span class="html-italic">p</span> &lt; 0.001 vs. naïve group; * <span class="html-italic">p</span> &lt; 0.05, vs. SD-pristane group. (<b>A</b>) Endothelial relaxation was induced by ACh (0.001–10 mM) in U46619 (0.003 mM) precontracted intact aorta rings from mice. The Ach-induced relaxant responses are expressed as a percentage of precontraction induced by U46619 (<span class="html-italic">n</span> = 7 per group). One-way ANOVA followed by Fisher’s LSD test results: * <span class="html-italic">p</span> &lt; 0.05; ** <span class="html-italic">p</span> &lt; 0.01 significant difference versus naïve control group (U46619), thromboxane receptor agonist 9,11-didesoxi-11α,9α-epoximetanoprostaglandina F2α.</p>
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<p>OLA dietary treatment modulated miRNAs and dnmt1 expression in pristane-induced nephritis. The relative renal expression of miRNAs: (<b>A</b>) miRNA-23b, (<b>B</b>) miRNA-146a, (<b>C</b>) miRNA-24-3p, and (<b>D</b>) miRNA-126, as well as (<b>E</b>) DNMT-1 mRNA from mice of the naïve, SD-pristane, and OLA-enriched diet groups, evaluated by RT-qPCR. Expression was normalized with MammU6 or β-actin, (<span class="html-italic">n</span> = 8). One-way ANOVA followed by Tukey’s post hoc test results: # <span class="html-italic">p</span> &lt; 0.05, ## <span class="html-italic">p</span> &lt; 0.01; ### <span class="html-italic">p</span> &lt; 0.001 vs. naïve group; * <span class="html-italic">p</span> &lt; 0,05, ** <span class="html-italic">p</span> &lt; 0.01; *** <span class="html-italic">p</span> &lt; 0.001, significant difference versus SD-pristane group.</p>
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13 pages, 3073 KiB  
Communication
Galectin-3 Mediates NETosis and Acts as an Autoantigen in Systemic Lupus Erythematosus-Associated Diffuse Alveolar Haemorrhage
by Shih-Yao Chen, Chung-Teng Wang, Ching-Yi Chen, Pin-Yu Kuo, Chrong-Reen Wang, Ai-Li Shiau, Cheng-Hsi Chang and Chao-Liang Wu
Int. J. Mol. Sci. 2023, 24(11), 9493; https://doi.org/10.3390/ijms24119493 - 30 May 2023
Cited by 6 | Viewed by 2090
Abstract
Systemic lupus erythematosus (SLE) is a systemic autoimmune disease with enhanced NETosis and impaired degradation of neutrophil extracellular traps (NETs). Galectin-3 is a β-galactoside binding protein and is associated with neutrophil functions as well as involved in mediating autoimmune disorders. In this study, [...] Read more.
Systemic lupus erythematosus (SLE) is a systemic autoimmune disease with enhanced NETosis and impaired degradation of neutrophil extracellular traps (NETs). Galectin-3 is a β-galactoside binding protein and is associated with neutrophil functions as well as involved in mediating autoimmune disorders. In this study, we plan to examine the associations of galectin-3 with the pathogenesis of SLE and NETosis. Galectin-3 expression levels were determined in peripheral blood mononuclear cells (PBMCs) of SLE patients for the association with lupus nephritis (LN) or correlation of SLE disease activity index 2000 (SLEDAI-2K). NETosis was observed in human normal and SLE and murine galectin-3 knockout (Gal-3 KO) neutrophils. Gal-3 KO and wild-type (WT) mice induced by pristane were used to evaluate disease signs, including diffuse alveolar haemorrhage (DAH), LN, proteinuria, anti-ribonucleoprotein (RNP) antibody, citrullinated histone 3 (CitH3) levels, and NETosis. Galectin-3 levels are higher in PBMCs of SLE patients compared with normal donors and positively correlated with LN or SLEDAI-2K. Gal-3 KO mice have higher percent survival and lower DAH, LN proteinuria, and anti-RNP antibody levels than WT mice induced by pristane. NETosis and citH3 levels are reduced in Gal-3 KO neutrophils. Furthermore, galectin-3 resides in NETs while human neutrophils undergo NETosis. Galectin-3-associated immune complex deposition can be observed in NETs from spontaneously NETotic cells of SLE patients. In this study, we provide clinical relevance of galectin-3 to the lupus phenotypes and the underlying mechanisms of galectin-3-mediated NETosis for developing novel therapeutic strategies targeting galectin-3 for SLE. Full article
(This article belongs to the Special Issue Autoimmune Diseases: A Swing Dance of the Immune Cells)
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<p>Expression of galectin-3 in patients with systemic lupus erythematosus (SLE) and mice with pristane-induced lupus. (<b>A</b>) Quantitative reverse transcription-polymerase chain reaction (qRT-PCR) of galectin-3 in PBMCs of SLE patients (SLE) and in the same cohort with (LN-Yes) or without (LN-Nil) lupus nephritis and normal donors (Normal). (<b>B</b>) The significance of correlation between the expression levels of galectin-3 and SLE disease activity index 2000 (SLEDAI-2K) was calculated using Pearson’s correlation coefficient. (<b>C</b>) Anti-galectin-3 antibody levels in sera of SLE patients and normal donors. (<b>D</b>) Female mice aged 8 weeks were injected with 500 μL of pristane or phosphate-buffered saline (PBS) via the intra-peritoneal routes. Mice died from diffuse alveolar haemorrhage (DAH) around week 4 after pristane injection, as demonstrated by H&amp;E staining. Immunohistochemical stainings of galectin-3 and moue IgG Fc in lung tissue sections from PBS and pristane-treated mice. Boxed areas are shown at higher magnification in the panels next to them. (<b>E</b>) Expression of galectin-3, citrullinated histone 3 (citH3), and histone 3 (H3) in lung tissue extracts from PBS and pristane-treated mice (n = 4). (<b>F</b>) Immunofluorescent stainings of myeloperoxidase (MPO, Texas red), and Ly6G (FITC) in lung tissue sections from PBS and pristane-treated WT and galectin-3 knockout (Gal-3 KO) mice. Boxed areas indicate MPO and Ly6G double-positive signals (×400 magnification). DAPI indicates nuclear staining. Values were presented as mean and SEM. Bars shown on the photomicrographs at ×40, ×100, and ×400 magnifications correspond to 500, 200, and 50 μm, respectively.</p>
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<p>Associations of galectin-3 and lupus manifestations in pristane-treated galectin-3 knockout (Gal-3 KO) mice. Female wild-type (WT) and Gal-3 KO mice aged 8 weeks were injected with 500 μL of pristane via the intra-peritoneal routes. (<b>A</b>) Representative images of DAH and inflammation from pristane-treated Gal-3 KO mice compared with WT counterparts, as demonstrated by H&amp;E staining (n = 3). Boxed areas are shown at higher magnification in the panels beneath them (<b>B</b>) Percent survival in pristane-induced WT and Gal-3 KO mice. (<b>C</b>) Representative images of renal sections from pristane-treated Gal-3 KO mice compared with their WT counterparts, as demonstrated by H&amp;E staining (×400 magnification). (<b>D</b>) Levels of proteinuria in pristane-induced WT and Gal-3 KO mice. (<b>E</b>) Levels of anti-RNP antibodies in sera from pristane-induced WT and Gal-3 KO mice, as determined by ELISA. (<b>F</b>) Expression of galectin-3, citH3, and H3 in lung tissue extracts from pristane-induced WT and Gal-3 KO mice, as determined by immunoblotting (n = 4). Values were presented as mean and SEM. Bars shown on the photomicrographs at ×40, ×100, and ×400 magnifications correspond to 500, 200, and 50 μm, respectively.</p>
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<p>Effects of galectin-3 on NETosis. (<b>A</b>) Representative images of neutrophils isolated from normal donors and analyzed at baseline (T0) or after stimulation with phorbol myristate acetate (PMA, 100 μM) for 4 h (T4). Cells were stained with DAPI for 10 min or with anti-human galectin-3 or with anti-human MPO antibody and followed by Texas-red conjugated secondary antibodies for immunofluorescence analysis. (<b>B</b>) Representative images and quantification of neutrophils isolated from normal donors and treated with lactose or glucose (20 and 50 mM) at T4. Cells were stained with DAPI for 10 min. Values were presented as mean and SEM (n = 3). (<b>C</b>) NETosis and (<b>D</b>) Galectin-3, citH3, and H3 expression in lipopolysaccharide (LPS, 20 μM)-treated neutrophils from WT and Gal-3 KO mice. (<b>E</b>) Representative images of PBMCs isolated from SLE patients or normal donors and analyzed at T0. Cells were stained with DAPI for 10 min or with rat anti-human galectin-3 antibody or sera from indicated donors and followed by Texas-red conjugated anti-rat or FITC-conjugated anti-human IgG secondary antibody for immunofluorescence analysis. Higher-magnification views of the merged images are shown on the far right. The yellow arrows indicate immune complex deposition. Bars shown on the photomicrographs at ×100 and ×400 magnifications correspond to 200 and 50 μm, respectively. * <span class="html-italic">p</span> &lt; 0.05, *** <span class="html-italic">p</span> &lt; 0.001.</p>
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16 pages, 5459 KiB  
Article
Meteoric Water Incursion, Crude Oil Degradation and Calcite Cementation of an Upper Cretaceous Reservoir in the Zagros Foreland Basin (Kurdistan Region of Iraq)
by Howri Mansurbeg, Ibrahim Mohialdeen, Ali Al-Juboury, Namam Salih, Mohammad Alsuwaidi, Salahadin Shahrokhi, Ihsan Al-Aasm, Rebar Mahmmud and Albert Permanyer
Water 2023, 15(10), 1953; https://doi.org/10.3390/w15101953 - 21 May 2023
Cited by 2 | Viewed by 2262
Abstract
Field observations, together with the results of gas chromatography–mass spectrometry (GC-MS) and stable carbon isotope analysis of bitumen, coupled with fluid inclusion microthermometry and stable isotope analyses of closely associated vug- and fracture-filling columnar calcite in the Upper Cretaceous Bekhme Formation, Kurdistan Region [...] Read more.
Field observations, together with the results of gas chromatography–mass spectrometry (GC-MS) and stable carbon isotope analysis of bitumen, coupled with fluid inclusion microthermometry and stable isotope analyses of closely associated vug- and fracture-filling columnar calcite in the Upper Cretaceous Bekhme Formation, Kurdistan Region of Iraq, suggest that the degradation of crude oil was caused by the regional incursion of meteoric waters. This incursion, which is interpreted to have occurred during tectonic uplift during the Zagros Orogeny, is evidenced by: (i) the depletion of n-alkanes and acyclic isoprenoid alkanes (pristane and phytane) in the bitumen; (ii) low δ13CVPDB values (−8.5‰ to −3.9‰) and δ18OVPDB values (−22.9‰ to −15.0‰), with more radiogenic Sr isotopic ratios (0.70771–0.70772) compared to Cretaceous seawater; and (iii) low salinity and low temperatures (20 to 40 °C) in fluid inclusions of the columnar calcite. This study demonstrates that regional meteoric water incursion into sedimentary basins can be linked to crude oil degradation accompanied by calcite cementation events in carbonate reservoirs. Full article
(This article belongs to the Section Oceans and Coastal Zones)
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<p>Geological map of northern Iraq (<b>A</b>) showing the distribution of the Bekhme Formation (green) and Bekhme Anticline (red line) in the Kurdistan Region (<b>B</b>) (after [<a href="#B14-water-15-01953" class="html-bibr">14</a>]).</p>
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<p>(<b>A</b>) Chronostratigraphic column for the study area (after [<a href="#B15-water-15-01953" class="html-bibr">15</a>]); (<b>B</b>) sampling location in the Bekhme Gorge, Kurdistan Region of northern Iraq; (<b>C</b>) outcrop showing the thick bitumen seeping out of the Bekhme Formation.</p>
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<p>(<b>A</b>–<b>C</b>) Field images showing bitumen accumulation and vertically arranged columnar calcite crystals (red arrows) occurring along a fracture and thrust surfaces in Bekhme Formation.</p>
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<p>(<b>A</b>) Total ion current and (<b>B</b>) <span class="html-italic">m</span>/<span class="html-italic">z</span> 57 chromatograms of saturated hydrocarbons showing a strong biodegradation of <span class="html-italic">n</span>-alkanes and an important unresolved complex mixture (UCM).</p>
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<p>Partially reconstructed chromatogram (<span class="html-italic">m</span>/<span class="html-italic">z</span> 191) displaying the tricyclic terpanes (<b>A</b>) and homohopanes (<b>B</b>) distributions in the extracted sample.</p>
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<p>Partially reconstructed chromatogram (<span class="html-italic">m</span>/<span class="html-italic">z</span> 217) showing the low-molecule pregnanes, regular steranes, and diasterane distributions in the extracted sample.</p>
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<p>Partially reconstructed chromatogram (<span class="html-italic">m</span>/<span class="html-italic">z</span> 231) displaying the triaromatic steroids distribution in the extracted sample.</p>
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<p>Cross-plot of the carbon and oxygen isotopic values of columnar calcite. These values are lower than what would be expected for calcite that was precipitated in equilibrium with Cretaceous seawater, as indicated by the pink box [<a href="#B28-water-15-01953" class="html-bibr">28</a>]. Note the positive correlation between carbon and oxygen isotopic values of the columnar calcite if the three outliers with unusually low δ<sup>18</sup>O values are removed.</p>
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<p>Cross-plot of strontium and oxygen isotopes [<a href="#B29-water-15-01953" class="html-bibr">29</a>] of columnar calcite showing that Sr isotopic ratios of the columnar calcite are higher than the postulated range for Cretaceous seawater.</p>
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<p>Cross-plot of homogenization temperatures versus oxygen isotopic values of calcite and dolomite. Note that saddle dolomite, equant calcite, and host dolostones have overlapping values, presumably owing to the genetic link between these carbonates, which is the flux of hydrothermal brines [<a href="#B30-water-15-01953" class="html-bibr">30</a>]. The negative oxygen isotopic values combined with the very low salinity of fluids responsible for the precipitation of columnar calcite suggest a meteoric origin.</p>
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<p>General paragenetic sequence reconstructed for the Bekhme Formation in relation to burial and orogenic events.</p>
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<p>Burial history curve of the study area shows a significant uplift/erosion of the Bekhme Formation in the Upper Cretaceous period (modified after [<a href="#B11-water-15-01953" class="html-bibr">11</a>,<a href="#B15-water-15-01953" class="html-bibr">15</a>,<a href="#B62-water-15-01953" class="html-bibr">62</a>]).</p>
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13 pages, 4499 KiB  
Article
The Differences of Nutrient Components in Edible and Feeding Coix Seed at Different Developmental Stages Based on a Combined Analysis of Metabolomics
by Xiaoyan Wei, Yong Li, Shufeng Zhou, Chao Guo, Xiaolong Dong, Qishuang Li, Juan Guo, Yanan Wang and Luqi Huang
Molecules 2023, 28(9), 3759; https://doi.org/10.3390/molecules28093759 - 27 Apr 2023
Cited by 2 | Viewed by 1732
Abstract
Coix lachryma-jobi L. is an excellent plant resource that has a concomitant function for medicine, foodstuff and forage in China. At present, the commonly used cultivar for both medicine and foodstuff is Xiaobaike, and the cultivar for foraging is Daheishan. However, differences in [...] Read more.
Coix lachryma-jobi L. is an excellent plant resource that has a concomitant function for medicine, foodstuff and forage in China. At present, the commonly used cultivar for both medicine and foodstuff is Xiaobaike, and the cultivar for foraging is Daheishan. However, differences in the internal composition of plants lead to the expression of different phenotypic traits. In order to comprehensively elucidate the differences in nutrient composition changes in Coix seeds, a non-targeted metabolomics method based on ultra-performance liquid chromatography quadrupole time-of-flight mass spectrometry (LC-Q-TOF-MS) was used to analyze the metabolic changes in Coix seeds at different developmental stages. An edible Coix relative (Xiaobaike) and a feeding Coix relative (Daheishan) were selected as the research subjects. In the metabolome analysis of Coix seed, 314 metabolites were identified and detected, among which organic acids, carbohydrates, lipids, nucleotides and flavonoids were the main components. As an important standard for evaluating the quality of Coix seed, seven lipids were detected, among which fatty acids included not only even-chain fatty acids, but also odd-chain fatty acids, which was the first time detecting a variety of odd-chain fatty acids in Coix seed. The analysis of the compound contents in edible and feeding-type Coix lachryma-jobi L. and the lipid content at the mature stage showed that, among them, arachidic acid, behenic acid, heptadecanoic acid, heneicosanoic acid and pristanic acid may be the key compounds affecting the lipid content. In addition, in the whole process of semen coicis maturation, edible and feeding Coix show similar trends, and changes in the third period show clear compounds in the opposite situation, suggesting that edible and feeding Coix not only guarantee the relative stability of species but also provide raw materials for genetic breeding. This study provides valuable information on the formation of the edible and medicinal qualities of Coix. Full article
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<p>PCA scores plot for DHS and XBK Coix seeds.</p>
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<p>Metabolites in different cultivars of Coix seeds: (<b>A</b>) Types of the identified metabolites from DHS and XBK. (<b>B</b>) Enrichment analysis of metabolite KEGG in <span class="html-italic">Coix lachryma-jobi</span> L.</p>
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<p>The types and quantities of identified lipids from Coix seeds.</p>
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<p>The number of differential metabolites in DHS and XBK.</p>
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<p>Statistics of pathway enrichment of differential metabolites in two varieties: (<b>A</b>) Statistics of pathway enrichment of differential metabolites in XBK. (<b>B</b>) Statistics of pathway enrichment of differential metabolites in DHS.</p>
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<p>Cluster analysis of identified differential metabolites from XBK.</p>
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<p>Cluster analysis of identified differential metabolites from DHS.</p>
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<p>Traits of <span class="html-italic">Coix lachryma-jobi</span> L: (<b>A</b>) Seedlings of <span class="html-italic">Coix lachryma-jobi</span> L. (<b>B</b>) Seeds of <span class="html-italic">Coix lachryma-jobi</span> L. after hulling. (<b>C</b>) Contents of lipids in Daheishan Coix seeds (DHS) and Xiaobaike Coix seeds (XBK) (mean <span class="html-italic">±</span> SD, <span class="html-italic">n</span> = 3).</p>
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<p>Samples of Coix seeds from different periods. (S and H stands for Daheishan and Xiaobaike Coix seeds, respectively. Scale bar = 1 cm).</p>
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14 pages, 3787 KiB  
Article
Biosurfactant Production from the Biodegradation of n-Paraffins, Isoprenoids and Aromatic Hydrocarbons from Crude Petroleum by Yarrowia lipolytica IMUFRJ 50682
by Tatiana Felix Ferreira, Fernanda Faria Martins, Caroline Alves Cayres, Priscilla F. F. Amaral, Débora de Almeida Azevedo and Maria Alice Zarur Coelho
Fermentation 2023, 9(1), 21; https://doi.org/10.3390/fermentation9010021 - 26 Dec 2022
Cited by 6 | Viewed by 2418
Abstract
Yarrowia lipolytica is a unique, strictly aerobic yeast with the ability to degrade efficiently hydrophobic substrates. In the present work, we evaluated the degrading potential of Yarrowia lipolytica IMUFRJ 50682, isolated from tropical estuarine water in Rio de Janeiro (Brazil), and the possible [...] Read more.
Yarrowia lipolytica is a unique, strictly aerobic yeast with the ability to degrade efficiently hydrophobic substrates. In the present work, we evaluated the degrading potential of Yarrowia lipolytica IMUFRJ 50682, isolated from tropical estuarine water in Rio de Janeiro (Brazil), and the possible biomolecules produced during this process. To investigate which crude oil compounds are degraded by Y. lipolytica IMUFRJ 50682, this microorganism was grown in a medium containing Marlim petroleum (19 °API, American Petroleum Institute gravity) at 28 °C and 160 rpm for 5 days. The residual petroleum was submitted to gas chromatograph-mass spectrometric analysis (GC-MS). The chromatographic fingerprints of the residual petroleum were compared with the abiotic control test incubated in the same conditions. Y. lipolytica assimilates high molecular weight hydrocarbons, such as n-alkanes (C11-C19), isoprenoids (pristane and phytane), aromatics with two or three aromatics rings (naphthalene, methylnaphthalenes, dimethylnaphthalenes, trimethylnaphthalenes, phenanthrene, methylphenanthrenes, dimethylphenanthrenes, anthracene). This strain was also capable of consuming more complex hydrocarbons, such as tricyclic terpanes. During this biodegradation, the emulsification index of the culture medium increased significantly, showing that biosurfactant molecules can be produced from this process. Therefore, Y. lipolytica IMUFRJ 50682 showed to be a potential crude oil degrading yeast, which can be used for bioremediation processes and simultaneously produce bioproducts of commercial interest. Full article
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<p>Cell growth profiles of <span class="html-italic">Y. lipolytica</span> IMUFRJ 50682 in seawater with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> oil (open circles), seawater with 2% glucose (black squares), and seawater with 2% glucose and 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> oil (grey diamonds).</p>
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<p>Images from the flasks after 120 h of <span class="html-italic">Y. lipolytica</span> IMUFRJ 50682 growth in (<b>A</b>) seawater with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> oil, (<b>B</b>) seawater with 2% glucose, and (<b>C</b>) seawater with 2% glucose and 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> oil.</p>
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<p>Total ion chromatograms of (<b>a</b>) crude oil (Marlim) (<b>b</b>) remaining oil after 120 h in the abiotic test and (<b>c</b>) remaining oil after 120 h of <span class="html-italic">Y. lipolytica</span>’s growth in seawater with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> of oil.</p>
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<p>Chromatographic fingerprints of <span class="html-italic">m</span>/<span class="html-italic">z</span> 85 of (<b>a</b>) remaining oil after 120 h in the abiotic test and (<b>b</b>) remaining oil after 120 h of <span class="html-italic">Y. lipolytica</span>’s growth in seawater with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> of oil.</p>
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<p>Chromatographic fingerprints of <span class="html-italic">m</span>/<span class="html-italic">z</span> 78 of (<b>a</b>) remaining oil after 120 h in the abiotic test and (<b>b</b>) remaining oil after 120 h of <span class="html-italic">Y. lipolytica</span>’s growth in seawater with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> of oil.</p>
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<p>Chromatographic fingerprints of <span class="html-italic">m</span>/<span class="html-italic">z</span> 191 of (<b>a</b>) remaining oil after 120 h in the abiotic test and (<b>b</b>) remaining oil after 120 h of <span class="html-italic">Y. lipolytica</span>’s growth in seawater with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> of oil.</p>
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<p>Chromatographic fingerprints of <span class="html-italic">m</span>/<span class="html-italic">z</span> 128, <span class="html-italic">m</span>/<span class="html-italic">z</span> 142, <span class="html-italic">m</span>/<span class="html-italic">z</span> 156, and <span class="html-italic">m</span>/<span class="html-italic">z</span> 170 of (<b>a</b>) remaining oil after 120 h in the abiotic test and (<b>b</b>) remaining oil after 120 h of <span class="html-italic">Y. lipolytica</span>’s growth in seawater with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> of oil.</p>
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<p>Chromatographic fingerprints of <span class="html-italic">m</span>/<span class="html-italic">z</span> 178, <span class="html-italic">m</span>/<span class="html-italic">z</span> 192, and <span class="html-italic">m</span>/<span class="html-italic">z</span> 206 of (<b>a</b>) remaining oil after 120 h in the abiotic test and (<b>b</b>) remaining oil after 120 h of <span class="html-italic">Y. lipolytica</span>’s growth in seawater with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> of oil.</p>
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<p>Bioproducts concentration profiles obtained by <span class="html-italic">Y. lipolytica</span> IMUFRJ 50682 in medium with 2% glucose and 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> oil (<b>a</b>), in medium with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> oil (<b>b</b>), and in medium with 2% glucose (<b>c</b>). Citric acid (open circles), lipase activity (black squares), emulsification index (EI) (grey diamonds).</p>
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<p>Optical microscopic observations of the culture medium after 96 h of <span class="html-italic">Y. lipolytica</span> IMUFRJ 50682 cultivation in medium with 2% glucose and 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> oil (<b>a</b>,<b>b</b>) and in medium with 1% <span class="html-italic">v</span>/<span class="html-italic">v</span> oil (<b>c</b>,<b>d</b>).</p>
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16 pages, 3928 KiB  
Article
Study on the Breeding and Characterization of High-Efficiency Oil-Degrading Bacteria by Mutagenesis
by Pan Zhang, Zhaoyang You, Tianfang Chen, Li Zhao, Jianguo Zhu, Weihong Shi, Qinwei Meng and Yongjun Sun
Water 2022, 14(16), 2544; https://doi.org/10.3390/w14162544 - 18 Aug 2022
Cited by 4 | Viewed by 2008
Abstract
In the present study, a high-efficiency petroleum hydrocarbon-degrading bacterium MX1 was screened from petrochemical wastewater sludge, and MX1 was identified using morphological, physiological, and biochemical experiments and combined with 16S rDNA. Results showed that the the MX1 strain belongs to Enterobacter sp. The [...] Read more.
In the present study, a high-efficiency petroleum hydrocarbon-degrading bacterium MX1 was screened from petrochemical wastewater sludge, and MX1 was identified using morphological, physiological, and biochemical experiments and combined with 16S rDNA. Results showed that the the MX1 strain belongs to Enterobacter sp. The degradation conditions were an incubation time of 18 days, temperature of 30 °C, pH of 7, and salinity of 2% (w/v), and the degradation proportion was 37.41% for 7 days. The combination of microwave and ultraviolet mutagenesis yielded the strain MXM3U2. The mutant strain had a petroleum hydrocarbon breakdown efficiency of 56.74% after 7 days of culture, and this value was 51.66% higher than the original strain. The number of strains and the rate of degradation of n-alkanes (C16, C24, C32, and C40) decreased steadily with the increase in carbon chains in the degradation test. GC/MS (Gas chromatography mass spectrometry) results showed that in the process of degrading crude oil, the hydrocarbons with carbon number C < 24 were degraded first, followed by hydrocarbons with carbon number C > 24. The strains had a good degradation effect on pristane, naphthalene, and phenanthrene. In this study, a high-efficiency petroleum hydrocarbon-degrading bacterium was screened via microwave-ultraviolet composite mutagenesis technology. Full article
(This article belongs to the Special Issue Water-Sludge-Nexus)
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<p>The screening of the oil-degrading bacteria.</p>
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<p>Rootless phylogenetic tree of 16S rDNA sequences between MX1 and related species of model strains in Enterobacter.</p>
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<p>TPHs removal efficiency of the MX1 strain under different culture conditions. (<b>a</b>) Culture time; (<b>b</b>) temperature; (<b>c</b>) pH; (<b>d</b>) the concentration of NaCl.</p>
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<p>TPHs removal efficiency of the MX1 strain under different culture conditions. (<b>a</b>) Culture time; (<b>b</b>) temperature; (<b>c</b>) pH; (<b>d</b>) the concentration of NaCl.</p>
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<p>Lethal rate curve for UV (<b>a</b>) and microwave (<b>b</b>) mutagenesis.</p>
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<p>TPHs removal efficiency of strains by UV (<b>a</b>) and microwave (<b>b</b>) mutagenesis.</p>
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<p>TPH removal efficiency by analysis of strain genetic stability.</p>
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<p>Growth of the strain on different n-alkanes as the sole carbon sources and its degradation of the alkanes (<b>a</b>–<b>d</b>) represented the case of n-alkanes C16, C24, C32, and C40, respectively.</p>
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<p>Growth of the strain on different n-alkanes as the sole carbon sources and its degradation of the alkanes (<b>a</b>–<b>d</b>) represented the case of n-alkanes C16, C24, C32, and C40, respectively.</p>
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14 pages, 3019 KiB  
Article
Metal–Metal Correlation of Biodegraded Crude Oil and Associated Economic Crops from the Eastern Dahomey Basin, Nigeria
by Saeed Mohammed, Mimonitu Opuwari, Salam Titinchi and Lilburne Cyster
Minerals 2022, 12(8), 960; https://doi.org/10.3390/min12080960 - 28 Jul 2022
Cited by 1 | Viewed by 1750
Abstract
The presence of heavy metals in plants from oil sand deposits may reflect mineralization resulting from petroleum biodegradation. Petroleum composition and heavy metal analyses were performed using thermal desorption gas chromatography and atomic absorption spectrophotometry on oil sand and plant root samples from [...] Read more.
The presence of heavy metals in plants from oil sand deposits may reflect mineralization resulting from petroleum biodegradation. Petroleum composition and heavy metal analyses were performed using thermal desorption gas chromatography and atomic absorption spectrophotometry on oil sand and plant root samples from the same localities in the Dahomey Basin. The results from the oil sand showed mainly heavy-end hydrocarbon components, humps of unresolved complex mixtures (UCM), absences of C6-C12 hydrocarbon chains, pristane, and phytane, indicating severe biodegradation. In addition, they showed varying concentrations of vanadium (2.699–7.708 ppm), nickel (4.005–11.716 ppm), chromium (1.686–5.733 ppm), cobalt (0.953–3.223 ppm), lead (0.649–0.978 ppm), and cadmium (0.188–0.461 ppm). Furthermore, these heavy metals were present in Citrus, Theobroma Cacao, Elaeis guineensis, and Cola. The chromium, nickel, vanadium, lead, cobalt, and cadmium concentrations in the Citrus were 7.475, 4.981, 0.551, 0.001, 0.806, and 0.177 ppm, respectively. For the Theobroma Cacao, the concentrations of chromium, nickel, vanadium, lead, cobalt, and cadmium were 7.095, 16.697, 2.151, 0.023, 3.942, and 0.254 ppm. Elaeis guineensis also showed the presence of chromium (32.685 ppm), nickel (32.423 ppm), vanadium (11.983 ppm), lead (0.190 ppm), cobalt (4.425 ppm), and cadmium (0.262 ppm). The amounts of chromium, nickel, vanadium, lead, cobalt, and cadmium in the Cola were 9.687, 9.157, 0.779, 0.037, 0.695, and 0.023 ppm. The World Health Organization’s (WHO) safe and permissible limits for Cd (0.003 ppm), Cr (0.1 ppm), Ni (0.05 ppm), and Pb (0.1 ppm) in agricultural soils were all exceeded in the oil sand. The presence of these metals in the oil sands and their uptake by the plants could potentially be toxic, resulting in high mortality. The metal–metal correlation of the plant’s rootsto the oil sand indicates the nonanthropogenic origin of the heavy metals, which leads to the conclusion that their source is related to the hydrocarbon accumulation in the Afowo sand. Full article
(This article belongs to the Special Issue The Relationship between Metal Deposits and Hydrocarbon Accumulation)
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<p>Maps showing the area of study. (<b>a</b>) Map of Africa showing the field of study in Nigeria. (<b>b</b>) Regional map of a part of southwestern Nigeria, indicating the well locations. The Ode-Aye-1 well is located at latitude 06°38′10.2″ N and longitude 004°45′59.7″ E. In contrast, Ilubinrin-1 is located at latitude 06°38′19.8″ N and longitude 004°49′47.9″ N. The maps were generated using G.P.S. Visualizer (G.P.S. Visualizer).</p>
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<p>Sedimentary basins in the Gulf of Guinea Province of West Africa from the United States Geological Survey (<a href="https://pubs.usgs.gov/bul/2207/C/" target="_blank">https://pubs.usgs.gov/bul/2207/C/</a>) (accessed on 2 May 2022) showing major structural features. The Mid-Atlantic Ridge and fractures are shown in the index map.</p>
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<p>Chromatogram of Ode-Aye-1 oil sand at a depth of 2.5 m. The response intensity (pA) is displayed on the <span class="html-italic">y</span>-axis, while the retention time is shown on the <span class="html-italic">x</span>-axis in minutes. The chromatogram showed the hump of the unresolved complex mixture (UCM) below the peaks, suggesting biodegraded oil.</p>
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<p>TD-GC result showing the chromatogram of Ode-Aye-1 oil sand at a depth of 4.1 m. The response intensity (pA) is displayed on the <span class="html-italic">y</span>-axis, while the retention time is shown on the <span class="html-italic">x</span>-axis in minutes. The chromatogram illustrated an unresolved complex mixture (UCM) below the peaks, indicating biodegraded oil.</p>
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<p>TD-GC result showing the chromatogram of Ilubinrin-1 oil sand at a depth of 2.0 m. The response intensity (pA) is displayed on the <span class="html-italic">y</span>-axis, while the retention time is shown on the <span class="html-italic">x</span>-axis in minutes. The chromatogram showed an unresolved complex mixture (UCM) below the peaks, indicating petroleum biodegradation.</p>
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<p>TD-GC result showing the chromatogram of Ilubinrin-1 oil sand at a depth of 3.1 m. The response intensity (pA) is displayed on the <span class="html-italic">y</span>-axis, while the retention time is shown on the <span class="html-italic">x</span>-axis in minutes. The presence of unresolved complex mixture (UCM) below the peaks suggests biodegraded oil.</p>
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<p>The concentration of Cr, Ni, V, Pb, Co, and Cd in oil sands.</p>
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<p>The concentration of Cr, Ni, V, Pb, Co, and Cd in the taproots of orange, cocoa, oil palm, and kola trees.</p>
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14 pages, 11688 KiB  
Article
The Sequence Stratigraphic Division and Depositional Environment of the Jurassic Yan’an Formation in the Pengyang Area, Southwestern Margin of the Ordos Basin, China
by Lianfu Hai, Caixia Mu, Qinghai Xu, Yongliang Sun, Hongrui Fan, Xiangyang Xie, Xiangcheng Wei, Chao Mei, Haibin Yu, Walter Manger and Jun Yang
Energies 2022, 15(14), 5310; https://doi.org/10.3390/en15145310 - 21 Jul 2022
Cited by 1 | Viewed by 1683
Abstract
Coal and organic-rich shale in the Yan’an Formation in the southwestern margin of the Ordos Basin are widely developed, which is an important fact for oil and gas exploration in China that has been widely explored for a long time. In this paper, [...] Read more.
Coal and organic-rich shale in the Yan’an Formation in the southwestern margin of the Ordos Basin are widely developed, which is an important fact for oil and gas exploration in China that has been widely explored for a long time. In this paper, detailed sequence division and sedimentary environment analyses of the Yan’an Formation in the Pengyang area on the southwestern margin of the Ordos Basin were conducted using field outcrops, drilling cores, logging, wavelet transform and organic geochemistry. The results showed that the succession consists of some units with distinctly different characteristics. Based on the petrographic assemblage and transform wavelet characteristics, the Yan’an Formation in this area can be divided into a long-term cycle, five medium-term cycles, and eleven short-term cycles, among which coal and carbonaceous shale were mainly developed in the short-term cycles I2, III1, III2, V1 and V2. Coal and organic-rich mud shale have been developed in the Yan’an Formation and plant debris in mudstone and coal is common, indicating the development of swamps and shallow water-covered depressions in this area. The sandstones showed parallel bedding, cross-bedding and scours, thus indicating fluvial deposits. The saturated hydrocarbon gas chromatographic parameters of mud shale showed that the pristane/phytane (Pr/Ph) ratio is 2.24–6.22, the Ph/nC18 ratio is 0.15–0.93, and the Pr/nC17 ratio is 0.97–2.78, supporting the finding that the organic matter has mainly originated from terrestrial sources. Full article
(This article belongs to the Special Issue Shale Oil and Gas Accumulation Mechanism)
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<p>Structural unit and geological map of Ordos Basin (modified from the work of Zhao et al., 2020 [<a href="#B6-energies-15-05310" class="html-bibr">6</a>]).</p>
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<p>Geological map of Yindonggou Coal Mine in Pengyang area (location in <a href="#energies-15-05310-f001" class="html-fig">Figure 1</a>). Key: Quaternary Holocene alluvial layers (Qh<sup>1al</sup>); Quaternary Pleistocene aeolian layers (Qp<sup>3-2eol</sup>); Ganhegou Formation of Neogene (N<sub>1</sub>g); Liwaxia Formation of Cretaceous (K<sub>1</sub>l); the fourth lithological member of the Heshangpu Formation of Cretaceous (K<sub>1</sub>h<sup>4</sup>); the third lithological member of the Heshangpu Formation of Cretaceous (K<sub>1</sub>h<sup>3</sup>); Yan’an Formation of Jurassic (J<sub>2y</sub>); Baota Formation of Ordovician (O<sub>3</sub>b); and Pingliang Formation of Ordovician (O<sub>2</sub>p). ZK1306 is the location and well name.</p>
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<p>The stratigraphic column of the well ZK1306.</p>
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<p>The continuous wavelet transform of gamma rays. (<b>a</b>) The gamma ray logging curve of Yan’an Formation of well ZK1306; (<b>b</b>) time−frequency chromatogram of wavelet-transform coefficient; (<b>c</b>) the curve of wavelet transforms with a scale of 330; (<b>d</b>) the curve of wavelet transforms with a scale of 170; and (<b>e</b>) the curve of wavelet transforms with a scale of 60. The red dashed line indicates the average value of scale a that could be used to identify the cycles.</p>
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<p>Stratigraphy and geophysical characteristics of the Yan’an Formation in well ZK1306. Key: Cal seam number (#1~#7); long−term cycle (L–T cycle); middle-term cycle (M–T cycle); short-term cycle (S–T cycle); gamma ray (GR).</p>
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<p>Typical field outcrop profile of Yan’an Formation in Pengyang area. (<b>A</b>) Thin-layered fine sandstone intercalated with mudstone in parallel bedding; (<b>B</b>) thick massive bedding fine sandstone; (<b>C</b>) cross-bedding with scour surface structure (red arrow); (<b>D</b>) horizontally bedded argillaceous siltstone; (<b>E</b>) coal line (red arrow) that is thick in the middle and gradually pinches out to both sides; and (<b>F</b>) grey-black mudstone with coal line, where the coal line is thinned to the left.</p>
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<p>Typical core photos of ZK1306. (<b>A</b>) Coarse sandstone, carbonaceous mudstone at the bottom with developed scour surface, 868.4 m; (<b>B</b>) grey-black mud shale showing carbonized plant debris development, 845.39 m; (<b>C</b>) grey mud shale containing a small amount of plant debris, 716.5 m; and (<b>D</b>) black carbonaceous mudstone with coal line, 692.8 m.</p>
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<p>Organic geochemical characteristics of shale in Yan’an Formation (on the basis of the work of Shanmugam, 1985 [<a href="#B39-energies-15-05310" class="html-bibr">39</a>]).</p>
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<p>The sedimentary environment and paleogeography of the Jurassic in the western Ordos Basin (modified after Zhang, 2010 [<a href="#B40-energies-15-05310" class="html-bibr">40</a>]).</p>
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17 pages, 1276 KiB  
Article
Functional Analysis of Autoantibody Signatures in Rheumatoid Arthritis
by Lisa Milchram, Anita Fischer, Jasmin Huber, Regina Soldo, Daniela Sieghart, Klemens Vierlinger, Stephan Blüml, Günter Steiner and Andreas Weinhäusel
Molecules 2022, 27(4), 1452; https://doi.org/10.3390/molecules27041452 - 21 Feb 2022
Cited by 3 | Viewed by 2853
Abstract
For the identification of antigenic protein biomarkers for rheumatoid arthritis (RA), we conducted IgG profiling on high density protein microarrays. Plasma IgG of 96 human samples (healthy controls, osteoarthritis, seropositive and seronegative RA, n = 24 each) and time-series plasma of a pristane-induced [...] Read more.
For the identification of antigenic protein biomarkers for rheumatoid arthritis (RA), we conducted IgG profiling on high density protein microarrays. Plasma IgG of 96 human samples (healthy controls, osteoarthritis, seropositive and seronegative RA, n = 24 each) and time-series plasma of a pristane-induced arthritis (PIA) rat model (n = 24 total) were probed on AIT’s 16k protein microarray. To investigate the analogy of underlying disease pathways, differential reactivity analysis was conducted. A total of n = 602 differentially reactive antigens (DIRAGs) at a significance cutoff of p < 0.05 were identified between seropositive and seronegative RA for the human samples. Correlation with the clinical disease activity index revealed an inverse correlation of antibodies against self-proteins found in pathways relevant for antigen presentation and immune regulation. The PIA model showed n = 1291 significant DIRAGs within acute disease. Significant DIRAGs for (I) seropositive, (II) seronegative and (III) PIA were subjected to the Reactome pathway browser which also revealed pathways relevant for antigen presentation and immune regulation; of these, seven overlapping pathways had high significance. We therefore conclude that the PIA model reflects the biological similarities of the disease pathogenesis. Our data show that protein array analysis can elucidate biological differences and pathways relevant in disease as well be a useful additional layer of omics information. Full article
(This article belongs to the Section Chemical Biology)
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<p>Study design. (<b>A</b>) sample cohort: 96 samples from RF- and CCP-positive (sero+), RF- and CCP- negative (sero-) RA, osteoarthritis and healthy human individuals and 24 samples from time-course pristane induced arthritis (PIA) and control animals were investigated. (<b>B</b>) IgG isolated from plasma was probed on AIT’s 16k microarray. (<b>C</b>) Data obtained from microarray scans was subjected to differential reactivity analysis (DRA) and correlation analysis with clinical disease activity index (CDAI) using BRB ArrayTools and RStudio elucidating differentially reactive antigens (DIRAGs) which were subsequently (<b>D</b>) in silico analyzed for dysregulated pathways.</p>
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<p>Volcano plot of seropositive versus seronegative RA. The unblocked class comparison elucidated <span class="html-italic">n</span> = 382 significant (<span class="html-italic">p</span> &lt; 0.05) DIRAGs with a fold-change &gt; 1.25 (−0.3219 and 0.3219 on the log2 scale, indicated as dashed line in the plot above). DIRAGs above the significance thresholds are indicated in blue (BRB ArrayTools [<a href="#B8-molecules-27-01452" class="html-bibr">8</a>] output per default). The sign of the fold-change is assigned in alphabetical order; hence, proteins higher reactive in seropositive RA are located on the left side of the plot.</p>
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<p>Intersection of significant higher reactive DIRAGs as Venn Diagram (<b>A</b>) and their respective <span class="html-italic">p</span>-values and the average fold-change as a forest plot (<b>B</b>). Results of the blocked analysis of the comparison seropositive versus seronegative RA was used, and PIA 7 vs. 24 days after correction for DIRAGs higher reactive in PBS animals. VennDiagram created with JVenn [<a href="#B9-molecules-27-01452" class="html-bibr">9</a>].</p>
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<p>Graphic representation (Venn diagram) of the involved genes of the top 25 pathways for the comparisons: seropositive RA vs. seronegative RA (seropos, red), seronegative RA vs. seropositive RA (blue) and 7- vs. 24-day PIA corrected for controls (PIA, green). Venn diagram created with JVenn [<a href="#B9-molecules-27-01452" class="html-bibr">9</a>].</p>
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<p>GOslim summaries for DIRAGs identified as higher reactive in (<b>A</b>) seropositive RA versus seronegative RA, (<b>B</b>) seronegative RA vs. seropositive RA and (<b>C</b>) PIA animals 7 and 24 days after disease induction corrected for signatures of control animals.</p>
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<p>The median difference between seronegative RA and seropositive RA is shown in the above Gardner–Altman estimation plot. Both groups are plotted on the left axes; the mean difference is plotted on a floating axis on the right as a bootstrap sampling distribution. The mean difference is depicted as a dot; the 95% confidence interval is indicated by the ends of the vertical error bar. The unpaired median difference between seronegative RA and seropositive RA is 0.2 [95.0%CI −6.45, 4.25]. The <span class="html-italic">p</span> value of the two-sided permutation <span class="html-italic">t</span>-test is 0.9 (calculation and plot generated by <a href="https://www.estimationstats.com" target="_blank">https://www.estimationstats.com</a> (accessed on 30 December 2021) according [<a href="#B41-molecules-27-01452" class="html-bibr">41</a>].</p>
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