Arshad Ali Shaikh, Joost Theo Petra Verhoeven, Rupesh Kumar Sinha, Suzanne C Dufour, Kapil Tahlan
Specialized metabolites produced by microorganisms found in ocean sediments display a wide range of clinically relevant bioactivities, including antimicrobial, anticancer, antiviral, and anti-inflammatory. Due to limitations in our ability to culture many benthic microorganisms under laboratory conditions, their potential to produce bioactive compounds remains underexplored. However, the advent of modern mass spectrometry technologies and data analysis methods for chemical structure prediction has aided in the discovery of such metabolites from complex mixtures. In this study, ocean sediments were collected from Baffin Bay (Canadian Arctic) and the Gulf of Maine for untargeted metabolomics using mass spectrometry. A direct examination of prepared organic extracts identified 1468 spectra, of which ∼45% could be annotated using in silico analysis methods. A comparable number of spectral features were detected in sediments collected from both locations, but 16S rRNA gene sequencing revealed a significantly more diverse bacterial community in samples from Baffin Bay. Based on spectral abundance, 12 specialized metabolites known to be associated with bacteria were selected for discussion. The application of metabolomics directly on marine sediments provides an avenue for culture-independent detection of metabolites produced under natural settings. The strategy can help prioritize samples for novel bioactive metabolite discovery using traditional workflows.
{"title":"A direct examination of microbial specialized metabolites associated with ocean sediments from Baffin Bay and the Gulf of Maine.","authors":"Arshad Ali Shaikh, Joost Theo Petra Verhoeven, Rupesh Kumar Sinha, Suzanne C Dufour, Kapil Tahlan","doi":"10.1139/cjm-2022-0205","DOIUrl":"https://doi.org/10.1139/cjm-2022-0205","url":null,"abstract":"<p><p>Specialized metabolites produced by microorganisms found in ocean sediments display a wide range of clinically relevant bioactivities, including antimicrobial, anticancer, antiviral, and anti-inflammatory. Due to limitations in our ability to culture many benthic microorganisms under laboratory conditions, their potential to produce bioactive compounds remains underexplored. However, the advent of modern mass spectrometry technologies and data analysis methods for chemical structure prediction has aided in the discovery of such metabolites from complex mixtures. In this study, ocean sediments were collected from Baffin Bay (Canadian Arctic) and the Gulf of Maine for untargeted metabolomics using mass spectrometry. A direct examination of prepared organic extracts identified 1468 spectra, of which ∼45% could be annotated using in silico analysis methods. A comparable number of spectral features were detected in sediments collected from both locations, but 16S rRNA gene sequencing revealed a significantly more diverse bacterial community in samples from Baffin Bay. Based on spectral abundance, 12 specialized metabolites known to be associated with bacteria were selected for discussion. The application of metabolomics directly on marine sediments provides an avenue for culture-independent detection of metabolites produced under natural settings. The strategy can help prioritize samples for novel bioactive metabolite discovery using traditional workflows.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 5","pages":"199-206"},"PeriodicalIF":2.8,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9381411","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Daqu is the natural starter for Nong-flavor Baijiu brewing. The effects of Daqu properties on the microbial community succession and their metabolites in fermented grains (FG) during Baijiu brewing were determined. These results showed that the effect of Daqu on the bacterial communities was stronger than that of the fungal communities. Compared with the conventional Daqu (DZ), Taikong (TK), and Qianghua (QH), Daqu significantly enhanced the content of volatile metabolites (especially esters) and ethanol when they were used, respectively, for FG fermentation. In the second round of fermentation, the relative abundance of Lactobacillus decreased, the content of lactic acid decreased, and that of caproic acid increased. In particular, the abundance of Lactobacillus was also reduced by 20% in FGs of the second round when TK Daqu was used than that in the respective first round. Partial least squares structural equation model analysis also showed that physicochemical parameters and Daqu properties significantly affected FG community structure and metabolism. This study provides a theoretical basis for further study on the effect of high-quality Daqu on the quality of fresh Baijiu and lays an important theoretical foundation for the stabilization of the Baijiu fermentation system based on Daqu.
{"title":"Effects of <i>Daqu</i> properties on the microbial community and their metabolites in fermented grains in Baijiu fermentation system.","authors":"Fengjiao Mao, Jun Huang, Rongqing Zhou, Hui Qin, Suyi Zhang, Xiaobo Cai, Chuanfeng Qiu","doi":"10.1139/cjm-2022-0213","DOIUrl":"https://doi.org/10.1139/cjm-2022-0213","url":null,"abstract":"<p><p><i>Daqu</i> is the natural starter for Nong-flavor Baijiu brewing. The effects of <i>Daqu</i> properties on the microbial community succession and their metabolites in fermented grains (FG) during Baijiu brewing were determined. These results showed that the effect of <i>Daqu</i> on the bacterial communities was stronger than that of the fungal communities. Compared with the conventional <i>Daqu</i> (DZ), Taikong (TK), and Qianghua (QH), <i>Daqu</i> significantly enhanced the content of volatile metabolites (especially esters) and ethanol when they were used, respectively, for FG fermentation. In the second round of fermentation, the relative abundance of <i>Lactobacillus</i> decreased, the content of lactic acid decreased, and that of caproic acid increased. In particular, the abundance of <i>Lactobacillus</i> was also reduced by 20% in FGs of the second round when TK <i>Daqu</i> was used than that in the respective first round. Partial least squares structural equation model analysis also showed that physicochemical parameters and <i>Daqu</i> properties significantly affected FG community structure and metabolism. This study provides a theoretical basis for further study on the effect of high-quality <i>Daqu</i> on the quality of fresh Baijiu and lays an important theoretical foundation for the stabilization of the Baijiu fermentation system based on <i>Daqu</i>.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 4","pages":"170-181"},"PeriodicalIF":2.8,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9238092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The nomenclature of prokaryotes is regulated by the rules of the International Code of Nomenclature of Prokaryotes (ICNP) and is based on the Linnaean binomial system. The current rules of the Code only cover the nomenclature of the cultivated minority. Proposals to incorporate the uncultivated majority of bacteria and archaea under the rules of the Code were recently rejected by the International Committee on Systematics of Prokaryotes. The provisional rank of Candidatus can be used to name uncultivated prokaryotes whose names cannot be validly published under the rules of the ICNP, but their names can now be validated under the Code of Nomenclature of Prokaryotes Described from Sequence Data (the SeqCode), which was recently established to cover the nomenclature of the uncultivated majority. Metagenomics, single-cell genomics, and high-throughput cultivation techniques have led to a flood of new organisms currently waiting to be named. Automated programs such as GAN and Protologger can assist researchers in naming and describing newly discovered prokaryotes, cultivated as well as uncultivated. However, Latin and Greek skills remain indispensable for proper quality control of names that must meet the standards set by the codes of nomenclature.
{"title":"Naming new taxa of prokaryotes in the 21st century.","authors":"Aharon Oren","doi":"10.1139/cjm-2022-0266","DOIUrl":"https://doi.org/10.1139/cjm-2022-0266","url":null,"abstract":"<p><p>The nomenclature of prokaryotes is regulated by the rules of the International Code of Nomenclature of Prokaryotes (ICNP) and is based on the Linnaean binomial system. The current rules of the Code only cover the nomenclature of the cultivated minority. Proposals to incorporate the uncultivated majority of bacteria and archaea under the rules of the Code were recently rejected by the International Committee on Systematics of Prokaryotes. The provisional rank of <i>Candidatus</i> can be used to name uncultivated prokaryotes whose names cannot be validly published under the rules of the ICNP, but their names can now be validated under the Code of Nomenclature of Prokaryotes Described from Sequence Data (the SeqCode), which was recently established to cover the nomenclature of the uncultivated majority. Metagenomics, single-cell genomics, and high-throughput cultivation techniques have led to a flood of new organisms currently waiting to be named. Automated programs such as GAN and Protologger can assist researchers in naming and describing newly discovered prokaryotes, cultivated as well as uncultivated. However, Latin and Greek skills remain indispensable for proper quality control of names that must meet the standards set by the codes of nomenclature.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 4","pages":"151-157"},"PeriodicalIF":2.8,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9607512","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Xiaohui Niu, Qian Li, Na Luan, Jia Liu, Michael Zhang, Jun An, Zuming Li, Zhihui Bai, Ran Xia, Zhichao Wu
This study explored the effects of Lactiplantibacillus plantarum (previously Lactobacillus plantarum) BW2013 on mucosal integrity and gut microbiota of mice with dextran sulfate sodium (DSS)-induced colitis. The results show that the clinical symptoms in DSS-modelled ulcerative colitis (UC) were improved by L. plantarum BW2013 via decreasing disease activity index scores and suppressing inflammatory cell infiltration. Furthermore, L. plantarum BW2013 decreased the levels of diamine oxidase activity, myeloperoxidase, and D-lactic acid. The mRNA expression of ZO-1, occludin, and claudin-1 was upregulated by L. plantarum BW2013, which also increased IL-10 and reduced TNF-α, IL-1β, and IL-6 in the colon. 16S rDNA sequencing showed that L. plantarum BW2013 enhanced α-diversity. L. plantarum BW2013 upregulated significantly the abundance of unidentfied Lachnospiraceae, Lactococcus, Rikenella, Lactobacillus, and Odoribacter, which had an inhibitory effect on inflammation and a protective effect on the integrity of the mucosa. These results demonstrate that L. plantarum BW2013 alleviates DSS-modelled UC by protecting mucosal integrity and ameliorating the composition of gut microbiota.
本研究探讨植物乳杆菌BW2013对葡聚糖硫酸钠(DSS)诱导结肠炎小鼠黏膜完整性和肠道菌群的影响。结果表明,植物乳杆菌BW2013通过降低疾病活动指数评分和抑制炎症细胞浸润来改善dss模型溃疡性结肠炎(UC)的临床症状。此外,L. plantarum BW2013降低了二胺氧化酶、髓过氧化物酶和d -乳酸的活性。植物L. plantarum BW2013上调ZO-1、occludin、claudin-1 mRNA表达,上调结肠组织中IL-10,降低TNF-α、IL-1β、IL-6。16S rDNA测序结果表明,L. plantarum BW2013增强了α-多样性。L. plantarum BW2013显著上调未鉴定的毛螺杆菌科、乳球菌、里氏菌、乳杆菌和臭杆菌的丰度,对炎症有抑制作用,对粘膜完整性有保护作用。这些结果表明,L. plantarum BW2013通过保护粘膜完整性和改善肠道菌群组成来缓解dss模型UC。
{"title":"<i>Lactiplantibacillus plantarum</i> BW2013 protects mucosal integrity and modulates gut microbiota of mice with colitis.","authors":"Xiaohui Niu, Qian Li, Na Luan, Jia Liu, Michael Zhang, Jun An, Zuming Li, Zhihui Bai, Ran Xia, Zhichao Wu","doi":"10.1139/cjm-2022-0092","DOIUrl":"https://doi.org/10.1139/cjm-2022-0092","url":null,"abstract":"<p><p>This study explored the effects of <i>Lactiplantibacillus plantarum</i> (previously <i>Lactobacillus plantarum</i>) BW2013 on mucosal integrity and gut microbiota of mice with dextran sulfate sodium (DSS)-induced colitis. The results show that the clinical symptoms in DSS-modelled ulcerative colitis (UC) were improved by <i>L. plantarum</i> BW2013 via decreasing disease activity index scores and suppressing inflammatory cell infiltration. Furthermore, <i>L. plantarum</i> BW2013 decreased the levels of diamine oxidase activity, myeloperoxidase, and D-lactic acid. The mRNA expression of ZO-1, occludin, and claudin-1 was upregulated by <i>L. plantarum</i> BW2013, which also increased IL-10 and reduced TNF-α, IL-1β, and IL-6 in the colon. 16S rDNA sequencing showed that <i>L. plantarum</i> BW2013 enhanced α-diversity. <i>L. plantarum</i> BW2013 upregulated significantly the abundance of unidentfied <i>Lachnospiraceae</i>, <i>Lactococcus</i>, <i>Rikenella</i>, <i>Lactobacillus</i>, and <i>Odoribacter</i>, which had an inhibitory effect on inflammation and a protective effect on the integrity of the mucosa. These results demonstrate that <i>L. plantarum</i> BW2013 alleviates DSS-modelled UC by protecting mucosal integrity and ameliorating the composition of gut microbiota.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 4","pages":"158-169"},"PeriodicalIF":2.8,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9237593","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Grant Johnson, Branden S J Gregorchuk, Arek Zubrzycki, Kurt Patrick Kolsun, Adrienne F A Meyers, Paul A Sandstrom, Michael Glen Becker
The GeneXpert® Xpert® Xpress SARS-CoV-2/Flu/RSV PLUS combination test (PLUS assay) received Health Canada approval in January 2022. The PLUS assay is similar to the SARS-CoV-2/Flu/RSV combination test, with modifications to improve assay robustness against circulating and emerging variants. The performance characteristics of the PLUS assay were assessed at the Lakeridge Health Oshawa Hospital Centre and the National Microbiology Laboratory of Canada. The PLUS assay was directly compared to the SARS-CoV-2/Flu/RSV combination test using SARS-CoV-2 culture from five variants and remnant clinical specimens collected across the coronavirus disease 2019 pandemic. This included 50 clinical specimens negative for all pathogens, 110 clinical specimens positive for SARS-CoV-2, influenza A, influenza B, RSVA, and(or) RSVB and an additional 11 mixed samples to screen for target interactions. The PLUS assay showed a high % agreement with the widely used SARS-CoV-2/Flu/RSV combination test. Based on these findings, the PLUS assay and the Xpert SARS-CoV-2/Flu/RSV combination test results are largely consistent with no observed difference in sensitivity, specificity, or time to result when challenged with various SARS-CoV-2 variants. The reported cycle threshold (Ct) values provided by the new PLUS assay were also unchanged, with the exception of a possible 1-2 decrease reported in Ct for RSVA across a limited sample size.
{"title":"Clinical evaluation of the GeneXpert<sup>®</sup> Xpert<sup>®</sup> Xpress SARS-CoV-2/Flu/RSV PLUS combination test.","authors":"Grant Johnson, Branden S J Gregorchuk, Arek Zubrzycki, Kurt Patrick Kolsun, Adrienne F A Meyers, Paul A Sandstrom, Michael Glen Becker","doi":"10.1139/cjm-2022-0204","DOIUrl":"https://doi.org/10.1139/cjm-2022-0204","url":null,"abstract":"<p><p>The GeneXpert<sup>®</sup> Xpert<sup>®</sup> Xpress SARS-CoV-2/Flu/RSV PLUS combination test (PLUS assay) received Health Canada approval in January 2022. The PLUS assay is similar to the SARS-CoV-2/Flu/RSV combination test, with modifications to improve assay robustness against circulating and emerging variants. The performance characteristics of the PLUS assay were assessed at the Lakeridge Health Oshawa Hospital Centre and the National Microbiology Laboratory of Canada. The PLUS assay was directly compared to the SARS-CoV-2/Flu/RSV combination test using SARS-CoV-2 culture from five variants and remnant clinical specimens collected across the coronavirus disease 2019 pandemic. This included 50 clinical specimens negative for all pathogens, 110 clinical specimens positive for SARS-CoV-2, influenza A, influenza B, RSVA, and(or) RSVB and an additional 11 mixed samples to screen for target interactions. The PLUS assay showed a high % agreement with the widely used SARS-CoV-2/Flu/RSV combination test. Based on these findings, the PLUS assay and the Xpert SARS-CoV-2/Flu/RSV combination test results are largely consistent with no observed difference in sensitivity, specificity, or time to result when challenged with various SARS-CoV-2 variants. The reported cycle threshold (Ct) values provided by the new PLUS assay were also unchanged, with the exception of a possible 1-2 decrease reported in Ct for RSVA across a limited sample size.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 3","pages":"146-150"},"PeriodicalIF":2.8,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10802480","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mai Farghaly, Michael F Hynes, Mohammad Nazari, Sylvia Lee Checkley, Karen Liljebjelke
Integrative and conjugative elements (ICEs) are self-transferable mobile genetic elements that play a significant role in disseminating antimicrobial resistance between bacteria via horizontal gene transfer. A recently identified ICE in a clinical isolate of Histophilus somni (ICEHs02) is 72 914 base pairs in length and harbours seven predicted antimicrobial resistance genes conferring resistance to tetracycline (tetR-tet(H)), florfenicol (floR), sulfonamide (Sul2), aminoglycosides (APH(3″)-Ib, APH(6)-Id, APH(3')-Ia), and copper (mco). This study investigated ICEHs02 host range, assessed effects of antimicrobial stressors on transfer frequency, and examined effects of ICEHs02 acquisition on hosts. Conjugation assays examined transfer frequency of ICEHs02 to H. somni and Pasteurella multocida strains. Polymerase chain reaction assays confirmed the presence of a circular intermediate, ICE-associated core genes, and cargo genes in recipient strains. Susceptibility testing examined ICEHs02-associated resistance phenotypes in recipient strains. Tetracycline and ciprofloxacin induction significantly increased the transfer rates of ICEHs02 in vitro. The copy numbers of the circular intermediate of ICEHs02 per chromosome exhibited significant increases of ∼37-fold after tetracycline exposure and ∼4-fold after ciprofloxacin treatment. The acquisition of ICEHs02 reduced the relative fitness of H. somni transconjugants (TG) by 28% (w = 0.72 ± 0.04) and the relative fitness of P. multocida TG was decreased by 15% (w = 0.85 ± 0.01).
整合和共轭元件(ICEs)是一种可自我转移的可移动遗传元件,在细菌间通过水平基因转移传播抗菌素耐药性方面起着重要作用。最近在somni Histophilus临床分离株(ICEHs02)中发现的ICE长度为72 914个碱基对,含有7个预测的抗菌素耐药基因,这些基因对四环素(tetret -tet(H))、氟苯尼醇(floR)、磺胺(Sul2)、氨基糖苷(APH(3″)-Ib、APH(6)-Id、APH(3′)-Ia)和铜(mco)具有耐药性。本研究调查了ICEHs02的宿主范围,评估了抗菌应激源对迁移频率的影响,并考察了ICEHs02获取对宿主的影响。偶联试验检测了ICEHs02向索姆尼嗜血杆菌和多杀性巴氏杆菌菌株转移的频率。聚合酶链反应实验证实在受体菌株中存在环状中间产物、ice相关核心基因和货物基因。药敏试验检测受体菌株中与icehs02相关的耐药表型。四环素和环丙沙星诱导显著提高ICEHs02的体外转移率。在四环素和环丙沙星处理后,每条染色体上ICEHs02环状中间体的拷贝数分别显著增加了~ 37倍和~ 4倍。ICEHs02基因的获得使嗜毒黑蝇转共轭子(TG)的相对适合度降低了28% (w = 0.72±0.04),使嗜毒黑蝇转共轭子(TG)的相对适合度降低了15% (w = 0.85±0.01)。
{"title":"Examination of the horizontal gene transfer dynamics of an integrative and conjugative element encoding multidrug resistance in <i>Histophilus somni</i>.","authors":"Mai Farghaly, Michael F Hynes, Mohammad Nazari, Sylvia Lee Checkley, Karen Liljebjelke","doi":"10.1139/cjm-2021-0349","DOIUrl":"https://doi.org/10.1139/cjm-2021-0349","url":null,"abstract":"<p><p>Integrative and conjugative elements (ICEs) are self-transferable mobile genetic elements that play a significant role in disseminating antimicrobial resistance between bacteria via horizontal gene transfer. A recently identified ICE in a clinical isolate of <i>Histophilus somni</i> (<i>ICEHs02</i>) is 72 914 base pairs in length and harbours seven predicted antimicrobial resistance genes conferring resistance to tetracycline (<i>tetR-tet(H)</i>), florfenicol (<i>floR</i>), sulfonamide (<i>Sul2</i>), aminoglycosides (<i>APH(3″)-Ib, APH(6)-Id, APH(3')-Ia</i>), and copper (<i>mco</i>). This study investigated <i>ICEHs02</i> host range, assessed effects of antimicrobial stressors on transfer frequency, and examined effects of <i>ICEHs02</i> acquisition on hosts. Conjugation assays examined transfer frequency of <i>ICEHs02</i> to <i>H. somni</i> and <i>Pasteurella multocida</i> strains. Polymerase chain reaction assays confirmed the presence of a circular intermediate, ICE-associated core genes, and cargo genes in recipient strains. Susceptibility testing examined <i>ICEHs02</i>-associated resistance phenotypes in recipient strains. Tetracycline and ciprofloxacin induction significantly increased the transfer rates of <i>ICEHs02</i> in vitro. The copy numbers of the circular intermediate of <i>ICEHs02</i> per chromosome exhibited significant increases of ∼37-fold after tetracycline exposure and ∼4-fold after ciprofloxacin treatment. The acquisition of <i>ICEHs02</i> reduced the relative fitness of <i>H. somni</i> transconjugants (TG) by 28% (<i>w</i> = 0.72 ± 0.04) and the relative fitness of <i>P. multocida</i> TG was decreased by 15% (<i>w</i> = 0.85 ± 0.01).</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 3","pages":"123-135"},"PeriodicalIF":2.8,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10811843","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Cordyceps farinosa, an entomopathogenic fungus, infects and leads to high mortality of Thitarodes armoricanus larvae, which die soon after the infection of C. farinose, usually before the colonization of Ophiocordyceps sinensis owing to competitive inhibition and fruiting body formation. Therefore, monitoring C. farinosa in the O. sinensis cultivation environment is critical for minimizing the C. farinosa infection-induced losses. In this study, we initially designed a PCR primer pair (Tar-1F/Tar-1R) through open reading frame prediction and homology comparison of the C. farinosa genome sequence. This primer pair can detect both C. farinosa and Samsoniella hepiali. To further distinguish, primers (ITS5-172/ITS4-95) were then designed to selectively amplify the large ribosomal subunit sequences in the C. farinosa genome. All these primers were applied in combination for detection of C. farinosa in soil samples. The sensitivity reached a detection limit of 1 × 106 spores/g soil. In addition, these primers can detect the presence of C. farinosa in dead T. armoricanus larval samples. This newly established rapid detection method provides important information for C. farinosa control during O. sinensis cultivation.
{"title":"Detection of the pathogenic fungus <i>Cordyceps farinosa</i> in the <i>Thitarodes armoricanus</i> soil-rearing environment based on nucleic acid targets.","authors":"Chaoqun Tong, Tian Li, Shisui Luo, Ruoni Chen, Shijiang Chen, Junhong Wei, Yuling Qing, Shaorong Qin, Guoqing Pan, Chunfeng Li, Zeyang Zhou","doi":"10.1139/cjm-2022-0165","DOIUrl":"https://doi.org/10.1139/cjm-2022-0165","url":null,"abstract":"<p><p><i>Cordyceps farinosa,</i> an entomopathogenic fungus, infects and leads to high mortality of <i>Thitarodes armoricanus</i> larvae, which die soon after the infection of <i>C. farinose</i>, usually before the colonization of <i>Ophiocordyceps sinensis</i> owing to competitive inhibition and fruiting body formation. Therefore, monitoring <i>C. farinosa</i> in the <i>O. sinensis</i> cultivation environment is critical for minimizing the <i>C. farinosa</i> infection-induced losses. In this study, we initially designed a PCR primer pair (Tar-1F/Tar-1R) through open reading frame prediction and homology comparison of the <i>C. farinosa</i> genome sequence. This primer pair can detect both <i>C. farinosa</i> and <i>Samsoniella hepiali</i>. To further distinguish, primers (ITS5-172/ITS4-95) were then designed to selectively amplify the large ribosomal subunit sequences in the <i>C. farinosa</i> genome. All these primers were applied in combination for detection of <i>C. farinosa</i> in soil samples. The sensitivity reached a detection limit of 1 × 10<sup>6</sup> spores/g soil. In addition, these primers can detect the presence of <i>C. farinosa</i> in dead <i>T. armoricanus</i> larval samples. This newly established rapid detection method provides important information for <i>C. farinosa</i> control during <i>O. sinensis</i> cultivation.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 3","pages":"136-145"},"PeriodicalIF":2.8,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10816108","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ramona Khanum, Pooi Yin Chung, Stuart C Clarke, Beek Yoke Chin
Lactoferrin is an innate glycoprotein with broad antibacterial and antibiofilm properties. The autonomous antibiofilm activity of lactoferrin against Gram-positive bacteria is postulated to involve the cell wall and biofilm components. Thus, the prevention of biomass formation and eradication of preformed biofilms by lactoferrin was investigated using a methicillin-resistant Staphylococcus epidermidis (MRSE) strain. Additionally, the ability of lactoferrin to modulate the expression of the biofilm-associated protein gene (bap) was studied. The bap gene regulates the production of biofilm-associated proteins responsible for bacterial adhesion and aggregation. In the in vitro biofilm assays, lactoferrin prevented biofilm formation and eradicated established biofilms for up to 24 and 72 h, respectively. Extensive eradication of MRSE biofilm biomass was accompanied by the significant upregulation of bap gene expression. These data suggest the interaction of lactoferrin with the biofilm components and cell wall of MRSE, including the biofilm-associated protein.
{"title":"Lactoferrin modulates the biofilm formation and <i>bap</i> gene expression of methicillin-resistant <i>Staphylococcus epidermidis</i>.","authors":"Ramona Khanum, Pooi Yin Chung, Stuart C Clarke, Beek Yoke Chin","doi":"10.1139/cjm-2022-0135","DOIUrl":"https://doi.org/10.1139/cjm-2022-0135","url":null,"abstract":"<p><p>Lactoferrin is an innate glycoprotein with broad antibacterial and antibiofilm properties. The autonomous antibiofilm activity of lactoferrin against Gram-positive bacteria is postulated to involve the cell wall and biofilm components. Thus, the prevention of biomass formation and eradication of preformed biofilms by lactoferrin was investigated using a methicillin-resistant <i>Staphylococcus epidermidis</i> (MRSE) strain. Additionally, the ability of lactoferrin to modulate the expression of the biofilm-associated protein gene (<i>bap</i>) was studied. The <i>bap</i> gene regulates the production of biofilm-associated proteins responsible for bacterial adhesion and aggregation. In the in vitro biofilm assays, lactoferrin prevented biofilm formation and eradicated established biofilms for up to 24 and 72 h, respectively. Extensive eradication of MRSE biofilm biomass was accompanied by the significant upregulation of <i>bap</i> gene expression. These data suggest the interaction of lactoferrin with the biofilm components and cell wall of MRSE, including the biofilm-associated protein.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 2","pages":"117-122"},"PeriodicalIF":2.8,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10653345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Abubakar Dar, Evans Were, Thomas Hilger, Zahir Ahmad Zahir, Maqshoof Ahmad, Azhar Hussain, Frank Rasche
Chemical weed control is an effective method, but has proved hazardous for humans, environment, and soil biodiversity. Use of allelopathic bacteria may be more efficient and sustainable weed control measure. The bacterial inoculants have never been studied in context of their interaction with weed root exudates and precursor-dependent production of the natural phytotoxins (cyanide, cytolytic enzymes and auxin) by these strains to understand their weed suppression and wheat growth promotion abilities. Therefore, root exudates of Avena fatua, Phalaris minor, Rumex dentatus, and wheat were quantified and their role in microbial root colonization and secondary metabolite production, i.e., cyanide, cytolytic enzymes, phenolics, and elevated auxin concentration, was studied. The results depicted l-tryptophan and glycine as major contributors of elevated cyanide and elevated levels in weed rhizosphere by the studied Pseudomonas strains, through their higher root colonization ability in weeds as compared with wheat. Furthermore, the higher root colonization also enhanced p-coumaric acid (photosynthesis inhibitor by impairing cytochrome c oxidase activity in plants) and cytolytic enzyme (root cell wall degradation) concentration in weed rhizosphere. In conclusion, the differential root colonization of wheat and weeds by these strains is responsible for enhancing weed suppression (enhancing phytotoxic effect) and wheat growth promotion (lowering phytotoxic effect).
{"title":"Bacterial secondary metabolites: possible mechanism for weed suppression in wheat.","authors":"Abubakar Dar, Evans Were, Thomas Hilger, Zahir Ahmad Zahir, Maqshoof Ahmad, Azhar Hussain, Frank Rasche","doi":"10.1139/cjm-2022-0181","DOIUrl":"https://doi.org/10.1139/cjm-2022-0181","url":null,"abstract":"<p><p>Chemical weed control is an effective method, but has proved hazardous for humans, environment, and soil biodiversity. Use of allelopathic bacteria may be more efficient and sustainable weed control measure. The bacterial inoculants have never been studied in context of their interaction with weed root exudates and precursor-dependent production of the natural phytotoxins (cyanide, cytolytic enzymes and auxin) by these strains to understand their weed suppression and wheat growth promotion abilities. Therefore, root exudates of <i>Avena fatua</i>, <i>Phalaris minor</i>, <i>Rumex dentatus</i>, and wheat were quantified and their role in microbial root colonization and secondary metabolite production, i.e., cyanide, cytolytic enzymes, phenolics, and elevated auxin concentration, was studied. The results depicted l-tryptophan and glycine as major contributors of elevated cyanide and elevated levels in weed rhizosphere by the studied <i>Pseudomonas</i> strains, through their higher root colonization ability in weeds as compared with wheat. Furthermore, the higher root colonization also enhanced <i>p-</i>coumaric acid (photosynthesis inhibitor by impairing cytochrome c oxidase activity in plants) and cytolytic enzyme (root cell wall degradation) concentration in weed rhizosphere. In conclusion, the differential root colonization of wheat and weeds by these strains is responsible for enhancing weed suppression (enhancing phytotoxic effect) and wheat growth promotion (lowering phytotoxic effect).</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 2","pages":"103-116"},"PeriodicalIF":2.8,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10604502","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Louis Garneau, Pascale B Beauregard, Sébastien Roy
In the present study, we report the in vitro interactions between Frankia sp. ACN10a and non-Frankia nodular endophytes (NFNE) isolated from alder. The supernatant of NFNE grown in nitrogen-replete medium had neutral or negative effects on Frankia growth; none had a stimulatory effect. Inhibitory effects were observed for supernatants of some NFNE, notably Micromonospora, Pseudomonas, Serratia and Stenotrophomonas isolates. However, some NFNE-Frankia coculture supernatants could stimulate Frankia growth when used as a culture medium supplement. This was observed for supernatants of Frankia cocultured with Microvirga and Streptomyces isolates. In nitrogen-limited conditions, cocultures of Frankia with some NFNE, including some rhizobia and Cytobacillus, resulted in higher total biomass than Frankia-only cultures, suggesting cooperation, while other NFNE were strongly antagonistic. Microscopic observation of cocultures also revealed compromised Frankia membrane integrity, and some differentiation into stress resistance-associated morphotypes such as sporangia and reproductive torulose hyphae (RTH). Furthermore, the coculture of Frankia with Serratia sp. isolates resulted in higher concentrations of the auxinic plant hormone indole-3-acetic acid and related indolic compounds in the culture supernatant. This study sheds new light on the breadth of microbial interactions that occur amongst bacteria that inhabit the understudied ecological niche of the alder nodule.
{"title":"Neighbours in nodules: the interactions between <i>Frankia</i> sp. ACN10a and non-<i>Frankia</i> nodular endophytes of alder.","authors":"Louis Garneau, Pascale B Beauregard, Sébastien Roy","doi":"10.1139/cjm-2022-0074","DOIUrl":"https://doi.org/10.1139/cjm-2022-0074","url":null,"abstract":"<p><p>In the present study, we report the in vitro interactions between <i>Frankia</i> sp. ACN10a and non-<i>Frankia</i> nodular endophytes (NFNE) isolated from alder. The supernatant of NFNE grown in nitrogen-replete medium had neutral or negative effects on <i>Frankia</i> growth; none had a stimulatory effect. Inhibitory effects were observed for supernatants of some NFNE, notably <i>Micromonospora, Pseudomonas, Serratia</i> and <i>Stenotrophomonas</i> isolates. However, some NFNE-<i>Frankia</i> coculture supernatants could stimulate <i>Frankia</i> growth when used as a culture medium supplement. This was observed for supernatants of <i>Frankia</i> cocultured with <i>Microvirga</i> and S<i>treptomyces</i> isolates. In nitrogen-limited conditions, cocultures of <i>Frankia</i> with some NFNE, including some rhizobia and <i>Cytobacillus,</i> resulted in higher total biomass than <i>Frankia</i>-only cultures, suggesting cooperation, while other NFNE were strongly antagonistic. Microscopic observation of cocultures also revealed compromised <i>Frankia</i> membrane integrity, and some differentiation into stress resistance-associated morphotypes such as sporangia and reproductive torulose hyphae (RTH). Furthermore, the coculture of <i>Frankia</i> with <i>Serratia</i> sp. isolates resulted in higher concentrations of the auxinic plant hormone indole-3-acetic acid and related indolic compounds in the culture supernatant. This study sheds new light on the breadth of microbial interactions that occur amongst bacteria that inhabit the understudied ecological niche of the alder nodule.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"69 2","pages":"88-102"},"PeriodicalIF":2.8,"publicationDate":"2023-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10653348","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}