Research in microbiology最新文献_第5页

Protein kinase A regulatory subunit is required for normal growth, zoosporogenesis, and pathogenicity in Phytophthora sojae 大豆疫霉正常生长、动物孢子发生和致病性需要蛋白激酶A调控亚基。

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104152

Yunxiang Zhang , Zhuo Zhang , Yue Chen , Xinqiu Tan , Yong Liu , Zhe Tian , Jinglin Wang , Xin Zhang , Deyong Zhang

{"title":"Protein kinase A regulatory subunit is required for normal growth, zoosporogenesis, and pathogenicity in Phytophthora sojae","authors":"Yunxiang Zhang , Zhuo Zhang , Yue Chen , Xinqiu Tan , Yong Liu , Zhe Tian , Jinglin Wang , Xin Zhang , Deyong Zhang","doi":"10.1016/j.resmic.2023.104152","DOIUrl":"10.1016/j.resmic.2023.104152","url":null,"abstract":"<div>Phytophthora sojae, one of the most devastating Oomycete pathogens, causes severe diseases that lead to economic loss in the soybean industry. The production of zoospores play a crucial role during the development of Phytophthora disease. In this work, CRISPR/Cas9 genome editing technology were used to obtain protein kinase A regulatory subunit (PsPkaR) knockout mutants. The role of PsPkaR in the production of zoospores and pathogenicity of P. sojae was analyzed. The overall findings indicate that PsPkaR is involved in regulating the growth process of P. sojae, primarily affecting the hyphal morphology and growth rate. Additionally, PsPkaR participates in the regulation of the release process of zoospores. Specifically, knocking-out PsPkaR resulted in incomplete cytoplasmic differentiation and uneven protoplast division, leading to abnormal release of zoospores. Furthermore, when the PsPkaR knockout mutants were inoculated on soybean leaves, the pathogenicity was significantly reduced compared to that of the wild-type and control strains. These findings of this study provide important clues and evidence regarding the role of the cAMP-PKA signaling pathway in the interaction between P. sojae and its host. This work contributes to a better understanding of the pathogenic mechanism of P. sojae and the development of corresponding prevention and control strategies.</div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":"175 4","pages":"Article 104152"},"PeriodicalIF":2.6,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89719387","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}

引用次数: 0

The stringent response is strongly activated in the antibiotic producing strain, Streptomyces coelicolor 产生抗生素的菌株 Streptomyces coelicolor 强烈激活了严格反应。

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104177

Clara Lejeune , David Cornu , Laila Sago , Virginie Redeker , Marie-Joelle Virolle

{"title":"The stringent response is strongly activated in the antibiotic producing strain, Streptomyces coelicolor","authors":"Clara Lejeune , David Cornu , Laila Sago , Virginie Redeker , Marie-Joelle Virolle","doi":"10.1016/j.resmic.2023.104177","DOIUrl":"10.1016/j.resmic.2023.104177","url":null,"abstract":"<div>S. lividans and S. coelicolor are phylogenetically closely related strains with different abilities to produce the same specialized metabolites. Previous studies revealed that the strong antibiotic producer, S. coelicolor, had a lower ability to assimilate nitrogen and phosphate than the weak producer, Streptomyces lividans, and this resulted into a lower growth rate. A comparative proteomic dataset was used to establish the consequences of these nutritional stresses on the abundance of proteins of the translational apparatus of these strains, grown in low and high phosphate availability. Our study revealed that most proteins of the translational apparatus were less abundant in S. coelicolor than in S. lividans whereas it was the opposite for ET-Tu 3 and a TrmA-like methyltransferase. The expression of the latter being known to be under the positive control of the stringent response whereas that of the other ribosomal proteins is under its negative control, this indicated the occurrence of a strong activation of the stringent response in S. coelicolor. Furthermore, in S. lividans, ribosomal proteins were more abundant in phosphate proficiency than in phosphate limitation suggesting that a limitation in phosphate, that was also shown to trigger RelA expression, contributes to the induction of the stringent response.</div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":"175 4","pages":"Article 104177"},"PeriodicalIF":2.6,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0923250823001547/pdfft?md5=88051488f17128fdd37532e9300b00d9&pid=1-s2.0-S0923250823001547-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139061838","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Elevated concentrations of polymyxin B elicit a biofilm-specific resistance mechanism in Vibrio cholerae 高浓度多粘菌素 B 在霍乱弧菌中激发生物膜特异性抗性机制

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104179

Julien Pauzé-Foixet, Annabelle Mathieu-Denoncourt, Marylise Duperthuy

{"title":"Elevated concentrations of polymyxin B elicit a biofilm-specific resistance mechanism in Vibrio cholerae","authors":"Julien Pauzé-Foixet, Annabelle Mathieu-Denoncourt, Marylise Duperthuy","doi":"10.1016/j.resmic.2023.104179","DOIUrl":"10.1016/j.resmic.2023.104179","url":null,"abstract":"<div>Vibrio cholerae can form biofilms in the aquatic environment and in the human intestine, facilitating the release of hyper-infectious aggregates. Due to the increasing antibiotic resistance, alternatives need to be found. One of these alternatives is antimicrobial peptides, including polymyxin B (PmB). In this study, we first investigated the resistance of V. cholerae O1 El Tor strain A1552 to various antimicrobials under aerobic and anaerobic conditions. An increased resistance to PmB is observed in anaerobiosis, with a 3-fold increase in the dose required for 50 % growth inhibition. We then studied the impact of the PmB on the formation and the degradation of V. cholerae biofilms to PmB. Our results show that PmB affects more efficiently biofilm formation under anaerobic conditions. On the other hand, preformed biofilms are susceptible to degradation by PmB at concentrations close to the minimal inhibitory concentration. At higher concentrations, we observe an opacification of the biofilm structures within 20 min post-treatment, suggesting a densification of the structure. This densification does not seem to result from the overexpression of matrix genes but rather from DNA release through massive cell lysis, likely forming a protective shield that limits the penetration of the PmB into the biofilm.</div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":"175 4","pages":"Article 104179"},"PeriodicalIF":2.6,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139376179","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}

引用次数: 0

Utilization of glycoprotein-derived N-acetylglucosamine-L-asparagine during Enterococcus faecalis infection depends on catabolic and transport enzymes of the glycosylasparaginase locus 粪肠球菌感染过程中对糖蛋白衍生的n-乙酰氨基葡萄糖- l -天冬酰胺的利用取决于糖基天冬酰胺酶位点的分解代谢和转运酶。

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104169

Victor Combret , Isabelle Rincé , Aurélie Budin-Verneuil , Cécile Muller , Josef Deutscher , Axel Hartke , Nicolas Sauvageot

{"title":"Utilization of glycoprotein-derived N-acetylglucosamine-L-asparagine during Enterococcus faecalis infection depends on catabolic and transport enzymes of the glycosylasparaginase locus","authors":"Victor Combret , Isabelle Rincé , Aurélie Budin-Verneuil , Cécile Muller , Josef Deutscher , Axel Hartke , Nicolas Sauvageot","doi":"10.1016/j.resmic.2023.104169","DOIUrl":"10.1016/j.resmic.2023.104169","url":null,"abstract":"<div>Enterococcus faecalis is a Gram-positive clinical pathogen causing severe infections. Its survival during infection depends on its ability to utilize host-derived metabolites, such as protein-deglycosylation products. We have identified in E. faecalis OG1RF a locus (ega) involved in the catabolism of the glycoamino acid N-acetylglucosamine-L-asparagine. This locus is separated into two transcription units, genes egaRP and egaGBCD1D2, respectively. RT-qPCR experiments revealed that the expression of the ega locus is regulated by the transcriptional repressor EgaR. Electromobility shift assays evidenced that N-acetylglucosamine-L-asparagine interacts directly with the EgaR protein, which leads to the transcription of the ega genes. Growth studies with egaG, egaB and egaC mutants confirmed that the encoded proteins are necessary for N-acetylglucosamine-L-asparagine catabolism. This glycoamino acid is transported and phosphorylated by a specific phosphotransferase system EIIABC components (OG1RF_10751, EgaB, EgaC) and subsequently hydrolyzed by the glycosylasparaginase EgaG, which generates aspartate and 6-P-N-acetyl-β-d-glucosaminylamine. The latter can be used as a fermentable carbon source by E. faecalis. Moreover, Galleria mellonella larvae had a significantly higher survival rate when infected with ega mutants compared to the wild-type strain, suggesting that the loss of N-acetylglucosamine-L-asparagine utilization affects enterococcal virulence.</div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":"175 4","pages":"Article 104169"},"PeriodicalIF":2.6,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136398986","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}

引用次数: 0

The role of intracellular β-glucosidase in cellulolytic response induction in filamentous fungus Penicillium verruculosum 丝状真菌疣青霉胞内β-葡萄糖苷酶在纤维素分解反应诱导中的作用

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104178

Valeriy Yu Kislitsin , Andrey M. Chulkin , Anna S. Dotsenko , Igor G. Sinelnikov , Arkady P. Sinitsyn , Aleksandra M. Rozhkova

引用次数: 0

Transcriptomic signature of bacteria exposed to benzalkonium chloride 暴露于苯扎氯铵的细菌转录组学特征。

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104151

Samantha J. McCarlie , Louis L. du Preez , Julio Castillo Hernandez , Charlotte E. Boucher , Robert R. Bragg

引用次数: 0

Comprehensive updates on the biological features and metabolic potential of the versatile extremophilic actinomycete Nocardiopsis dassonvillei 多用途嗜极放线菌的生物学特性和代谢潜力的全面更新。

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104171

Shivani Bhairamkar, Pratik Kadam, H. Anjulal, Avani Joshi, Riddhi Chaudhari, Dimpal Bagul, Vaishali Javdekar, Smita Zinjarde

引用次数: 0

Prevalence, antimicrobial resistance, and genetic lineages of nasal Staphylococcus aureus among medical students at a Spanish University: detection of the MSSA-CC398-IEC-type-C subclade 西班牙一所大学医学生鼻腔金黄色葡萄球菌的流行率、抗菌药耐药性和基因系：发现 MSSA-CC398-IEC-C 型亚支系

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104176

Nerea C. Rosales-González , Margarita González-Martín , Idris Nasir Abdullahi , María Teresa Tejedor-Junco , Javier Latorre-Fernández , Carmen Torres

{"title":"Prevalence, antimicrobial resistance, and genetic lineages of nasal Staphylococcus aureus among medical students at a Spanish University: detection of the MSSA-CC398-IEC-type-C subclade","authors":"Nerea C. Rosales-González , Margarita González-Martín , Idris Nasir Abdullahi , María Teresa Tejedor-Junco , Javier Latorre-Fernández , Carmen Torres","doi":"10.1016/j.resmic.2023.104176","DOIUrl":"10.1016/j.resmic.2023.104176","url":null,"abstract":"<div>Medical students could be a potential source of Staphylococcus aureus transmission to patients. This cross-sectional study involved samples collected from both nasal nostrils. Samples were processed for S. aureus recovery; the antimicrobial resistance (AMR) phenotype was determined by disc diffusion assays and the spa types and AMR genotypes by PCR/sequencing. A structured questionnaire was administered to students to collate data related to potential risk factors of nasal colonization. Ninety-eight students were included, 50 % were colonized by S. aureus and 12.2 % by MRSA. The mecA gene was detected in all MRSA isolates. The MSSA-CC398-IEC-type C lineage was found among 16.3 % of nasal carriers, of which t571 was the predominant spa-type. MRSA isolates were ascribed to spa types t2226 (CC5, 12 isolates) and t3444 (new spa type, 1 isolate). All MRSA were multi-drug resistant and MSSA were predominantly resistant to erythromycin-clindamycin (inducible-type, mediated by ermT gene). High rates of S. aureus and MRSA nasal carriages were observed in this study. The predominance of the CC398 lineage among MSSA (emergent invasive lineage) represent a relevant finding of public health concern. The role of medical students as potential source of MRSA and MSSA-CC398 transmissions in hospital and community needs to be elucidated in detail.</div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":"175 4","pages":"Article 104176"},"PeriodicalIF":2.6,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0923250823001535/pdfft?md5=1eecc509ff957656d75b6c6b8f0f9eaa&pid=1-s2.0-S0923250823001535-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139028083","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Review of techniques for the in-situ sterilization of soil contaminated with Bacillus anthracis spores or other pathogens 审查对受炭疽杆菌孢子或其他病原体污染的土壤进行原位灭菌的技术。

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104175

Joseph P. Wood

引用次数: 0

Assessment of the growth inhibition and anti-biofilm activity of aptamer (PmA2G02) against Proteus mirabilis 1429T 适体（PmA2G02）对奇异变形杆菌1429T的生长抑制和抗生物膜活性的评估。

IF 2.6 4区生物学

Research in microbiology Pub Date : 2024-03-01 DOI: 10.1016/j.resmic.2023.104105

Rajalakshmi Elumalai , Archana Vishwakarma , Anandkumar Balakrishnan , Mohandass Ramya

{"title":"Assessment of the growth inhibition and anti-biofilm activity of aptamer (PmA2G02) against Proteus mirabilis 1429T","authors":"Rajalakshmi Elumalai , Archana Vishwakarma , Anandkumar Balakrishnan , Mohandass Ramya","doi":"10.1016/j.resmic.2023.104105","DOIUrl":"10.1016/j.resmic.2023.104105","url":null,"abstract":"<div>Proteus mirabilis is known to cause Catheter-associated urinary tract infections (CAUTIs), which exhibit virulence factors linked to forming biofilms. Aptamers have recently been explored as potential anti-biofilm agents. This study demonstrates the anti-biofilm activity of aptamer (PmA2G02) targeting P. mirabilis 1429T, a pathogenic bacteria known to cause Catheter-associated urinary tract infections (CAUTIs). The studied aptamer inhibited biofilm formation, swarming motility, and cell viability at a concentration of 3 μM. The study also showed that the PmA2G02 had a binding affinity towards fimbrial outer membrane usher protein (PMI1466), flagellin protein (PMI1619), and regulator of swarming behavior (rsbA), which are responsible for adhesion, motility, and quorum sensing, respectively. Crystal violet assay, SEM, and confocal imaging confirmed the effectiveness of the PmA2G02 as an anti-biofilm agent. Moreover, as verified by qPCR, the expression levels of fimD, fliC2, and rsbA were significantly reduced compared to the untreated group. This study suggests that aptamer may be a potential alternative to traditional antibiotics for the treatment of CAUTIs caused by P. mirabilis. These findings shed light on the mechanisms by which the aptamer inhibits biofilm formation.</div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":"175 3","pages":"Article 104105"},"PeriodicalIF":2.6,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9769763","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}

引用次数: 0