Research in microbiology最新文献

筛选
英文 中文
The influence of the phylum Planctomycetota in the environmental resistome Planctomycetota 门在环境抗性组中的影响。
IF 2.5 4区 生物学
Research in microbiology Pub Date : 2024-07-01 DOI: 10.1016/j.resmic.2024.104196
Ofélia Godinho , Damien P. Devos , Sandra Quinteira , Olga M. Lage
{"title":"The influence of the phylum Planctomycetota in the environmental resistome","authors":"Ofélia Godinho ,&nbsp;Damien P. Devos ,&nbsp;Sandra Quinteira ,&nbsp;Olga M. Lage","doi":"10.1016/j.resmic.2024.104196","DOIUrl":"10.1016/j.resmic.2024.104196","url":null,"abstract":"<div><p>Antimicrobial resistance is one of the leading causes of death worldwide and research on this topic has been on the spotlight for a long time. More recently and in agreement with the One Health Approach, the focus has moved towards the environmental resistome. Members of the phylum <em>Planctomycetota</em> are ubiquitously present in the environment including in hotspots for antimicrobial resistance selection and dissemination. Furthermore, phenotypic broad-range resistance has been observed in diverse members of this phylum. Here we review the evidence available on antimicrobial resistance in the underexploited <em>Planctomycetota</em> and highlight key aspects for future studies.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"PeriodicalIF":2.5,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0923250824000226/pdfft?md5=44d481a10d48dfcd6c3b140cfe329afb&pid=1-s2.0-S0923250824000226-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140102356","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
Multiple SigB homologues govern the transcription of the ssgBp promoter in the sporulation–specific ssgB gene in Streptomyces coelicolor A3(2) 多个 SigB 同源物控制着 A3(2)链霉菌孢子特异性 ssgB 基因中 ssgBp 启动子的转录。
IF 2.5 4区 生物学
Research in microbiology Pub Date : 2024-07-01 DOI: 10.1016/j.resmic.2024.104201
Rachel Javorova , Beatrica Sevcikova , Bronislava Rezuchova, Renata Novakova, Filip Opaterny, Dominika Csolleiova, Lubomira Feckova, Jan Kormanec
{"title":"Multiple SigB homologues govern the transcription of the ssgBp promoter in the sporulation–specific ssgB gene in Streptomyces coelicolor A3(2)","authors":"Rachel Javorova ,&nbsp;Beatrica Sevcikova ,&nbsp;Bronislava Rezuchova,&nbsp;Renata Novakova,&nbsp;Filip Opaterny,&nbsp;Dominika Csolleiova,&nbsp;Lubomira Feckova,&nbsp;Jan Kormanec","doi":"10.1016/j.resmic.2024.104201","DOIUrl":"10.1016/j.resmic.2024.104201","url":null,"abstract":"<div><p>Unlike <em>Bacillus subtilis</em>, <em>Streptomyces coelicolor</em> contains nine SigB homologues of the stress-response sigma factor SigB. By using a two-plasmid system, we previously identified promoters recognized by these sigma factors. Almost all promoters were recognized by several SigB homologues. However, no specific sequences of these promoters were found. One of these promoters, <em>ssgBp</em>, was selected to examine this cross-recognition in the native host. It controls the expression of the sporulation-specific gene <em>ssgB</em>. Using a luciferase reporter, the activity of this promoter in <em>S. coelicolor</em> and nine mutant strains lacking individual <em>sigB</em> homologous genes showed that <em>sgBp</em> is dependent on three sigma factors, SigH, SigN, and SigI. To determine which nucleotides in the-10 region are responsible for the selection of a specific SigB homologue, promoters mutated at the last three nucleotide positions were tested in the two-plasmid system. Some mutant promoters were specifically recognized by a distinct set of SigB homologues. Analysis of these mutant promoters in the native host showed the role of these nucleotides. A conserved nucleotide A at position 5 was essential for promoter activity, and two variable nucleotides at positions 4 and 6 were responsible for the partial selectivity of promoter recognition by SigB homologues.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"PeriodicalIF":2.5,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140207491","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
Biochemical characterization and mutational analysis of the NurA protein from the hyperthermophilic euryarchaeon Thermococcus barophilus Ch5 超嗜热真菌嗜热球菌 Ch5 的 NurA 蛋白的生化特征和突变分析。
IF 2.5 4区 生物学
Research in microbiology Pub Date : 2024-07-01 DOI: 10.1016/j.resmic.2024.104189
Guangyu Ma , Tan Lin , Peng Cao , Philippe Oger , Kunming Dong , Li Miao , Likui Zhang
{"title":"Biochemical characterization and mutational analysis of the NurA protein from the hyperthermophilic euryarchaeon Thermococcus barophilus Ch5","authors":"Guangyu Ma ,&nbsp;Tan Lin ,&nbsp;Peng Cao ,&nbsp;Philippe Oger ,&nbsp;Kunming Dong ,&nbsp;Li Miao ,&nbsp;Likui Zhang","doi":"10.1016/j.resmic.2024.104189","DOIUrl":"10.1016/j.resmic.2024.104189","url":null,"abstract":"<div><p>Archaeal NurA protein plays a key role in producing 3′-single stranded DNA used for homologous recombination repair, together with HerA, Mre11, and Rad50. Herein, we describe biochemical characteristics and roles of key amino acid residues of the NurA protein from the hyperthermophilic euryarchaeon <em>Thermococcus barophilus</em> Ch5 (Tba-NurA). Tba-NurA possesses 5′–3′ exonuclease activity for degrading DNA, displaying maximum efficiency at 45 °C–65 °C and at pH 8.0 in the presence of Mn<sup>2+</sup>. The thermostable Tba-NurA also possesses endonuclease activity capable of nicking plasmid DNA and circular ssDNA. Mutational data demonstrate that residue D49 of Tba-NurA is essential for exonuclease activity and is involved in binding ssDNA since the D49A mutant lacked exonuclease activity and reduced ssDNA binding. The R96A and R129A mutants had no detectable dsDNA binding, suggesting that residues R96 and R129 are important for binding dsDNA. The abolished degradation activity and reduced dsDNA binding of the D120A mutant suggest that residue D120 is essential for degradation activity and dsDNA binding. Additionally, residues Y392 and H400 are important for exonuclease activity since these mutations resulted in exonuclease activity loss. To our knowledge, it is the first report on biochemical characterization and mutational analysis of the NurA protein from <em>Thermococcus</em>.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"PeriodicalIF":2.5,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139973333","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
Isolation of a PRD1-like phage uncovers the carriage of three putative conjugative plasmids in clinical Burkholderia contaminans 一种类似 PRD1 的噬菌体的分离发现了临床伯克霍尔德菌污染菌中携带的三种假定共轭质粒
IF 2.5 4区 生物学
Research in microbiology Pub Date : 2024-07-01 DOI: 10.1016/j.resmic.2024.104202
Cassandra R. Stanton , Steve Petrovski , Steven Batinovic
{"title":"Isolation of a PRD1-like phage uncovers the carriage of three putative conjugative plasmids in clinical Burkholderia contaminans","authors":"Cassandra R. Stanton ,&nbsp;Steve Petrovski ,&nbsp;Steven Batinovic","doi":"10.1016/j.resmic.2024.104202","DOIUrl":"10.1016/j.resmic.2024.104202","url":null,"abstract":"<div><p>The <em>Burkholderia cepacia</em> complex (Bcc) is a group of increasingly multi-drug resistant opportunistic bacteria. This resistance is driven through a combination of intrinsic factors and the carriage of a broad range of conjugative plasmids harbouring virulence determinants. Therefore, novel treatments are required to treat and prevent further spread of these virulence determinants. In the search for phages infective for clinical Bcc isolates, CSP1 phage, a PRD1-like phage was isolated. CSP1 phage was found to require pilus machinery commonly encoded on conjugative plasmids to facilitate infection of Gram-negative bacteria genera including <em>Escherichia</em> and <em>Pseudomonas</em>. Whole genome sequencing and characterisation of one of the clinical <em>Burkholderia</em> isolates revealed it to be <em>Burkholderia contaminans</em>. <em>B. contaminans</em> 5080 was found to contain a genome of over 8 Mbp encoding multiple intrinsic resistance factors, such as efflux pump systems, but more interestingly, carried three novel plasmids encoding multiple putative virulence factors for increased host fitness, including antimicrobial resistance. Even though PRD1-like phages are broad host range, their use in novel antimicrobial treatments shouldn't be dismissed, as the dissemination potential of conjugative plasmids is extensive. Continued survey of clinical bacterial strains is also key to understanding the spread of antimicrobial resistance determinants and plasmid evolution.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"PeriodicalIF":2.5,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0923250824000330/pdfft?md5=db2b5303bfc7ffe5081639e2734bdbd5&pid=1-s2.0-S0923250824000330-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140613764","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
Whole genome analysis, thermal and UV-tolerance of Lactococcus phage BIM BV-114 isolated from cheese brine 从奶酪盐水中分离出的乳球菌噬菌体 BIM BV-114 的全基因组分析、耐热性和耐紫外线性。
IF 2.5 4区 生物学
Research in microbiology Pub Date : 2024-07-01 DOI: 10.1016/j.resmic.2024.104203
Aliaksandra Herasimovich, Artur Akhremchuk, Leonid Valentovich, Anastasiya Sidarenka
{"title":"Whole genome analysis, thermal and UV-tolerance of Lactococcus phage BIM BV-114 isolated from cheese brine","authors":"Aliaksandra Herasimovich,&nbsp;Artur Akhremchuk,&nbsp;Leonid Valentovich,&nbsp;Anastasiya Sidarenka","doi":"10.1016/j.resmic.2024.104203","DOIUrl":"10.1016/j.resmic.2024.104203","url":null,"abstract":"<div><p><em>Lactococcus</em> phages that belong to the genus <em>Ceduovirus</em> are among the three most frequently isolated phage groups infecting <em>Lactococcus lactis</em> starter strains in dairy plants. In this study, we characterized virulent <em>Lactococcus</em> phage BIM BV-114 isolated from industrial cheese brine in Belarus and identified as <em>Ceduovirus</em>. The bacteriophage demonstrated a relatively short lytic cycle (latent period of 23 ± 5 min, lysis time of 90 ± 5 min), high thermal stability (inactivation after 7 min at 95 °C in skimmed milk) and tolerance to UV radiation (inactivation time – 15 min), indicating adaptation for better persistence in dairy facilities. The genome of the phage BIM BV-114 (21 499 bp; 37 putative open reading frames) has a similar organization to that of other <em>Ceduovirus</em> phages. <em>RLf1_00140</em> and <em>RLf_00050</em> gene products, found in the early genes region, may be involved in the sensitivity of phage to the lactococcal abortive infection mechanisms AbiV and AbiQ, respectively. Furthermore, nucleotide deletion, observed in the middle region of the gene encoding putative tape measure protein (RLf1_00300), is possibly responsible for increased thermal tolerance of phage BIM BV-114. Together, these findings will contribute to a better knowledge of virulent <em>Lactococcus</em> phages and the development of effective methods of their control for dairy technologies.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"PeriodicalIF":2.5,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140857949","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
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 ,&nbsp;Zhuo Zhang ,&nbsp;Yue Chen ,&nbsp;Xinqiu Tan ,&nbsp;Yong Liu ,&nbsp;Zhe Tian ,&nbsp;Jinglin Wang ,&nbsp;Xin Zhang ,&nbsp;Deyong Zhang","doi":"10.1016/j.resmic.2023.104152","DOIUrl":"10.1016/j.resmic.2023.104152","url":null,"abstract":"<div><p><span><em>Phytophthora</em><em> sojae</em></span><span>, 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 </span><em>Phytophthora</em><span> 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 </span><em>P. sojae</em> was analyzed. The overall findings indicate that PsPkaR is involved in regulating the growth process of <em>P. sojae</em><span>, 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<span> 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 </span></span><em>P. sojae</em> and its host. This work contributes to a better understanding of the pathogenic mechanism of <em>P. sojae</em> and the development of corresponding prevention and control strategies.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"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
Termitidicoccus mucosus gen. nov. sp. nov. a novel Verrucomicrobiota species isolated from Reticulitermes chinensis gives insights of high adaptability of symbiotic bacteria to termite gut ecosystem 从网纹蚁中分离出的新的白蚁微生物群(Termitidicoccus mucosus gen.
IF 2.6 4区 生物学
Research in microbiology Pub Date : 2024-05-01 DOI: 10.1016/j.resmic.2023.104173
Cheng Mei , Yu Shi , Yu Wang , Zhengyong Qiu , Hong Yang
{"title":"Termitidicoccus mucosus gen. nov. sp. nov. a novel Verrucomicrobiota species isolated from Reticulitermes chinensis gives insights of high adaptability of symbiotic bacteria to termite gut ecosystem","authors":"Cheng Mei ,&nbsp;Yu Shi ,&nbsp;Yu Wang ,&nbsp;Zhengyong Qiu ,&nbsp;Hong Yang","doi":"10.1016/j.resmic.2023.104173","DOIUrl":"10.1016/j.resmic.2023.104173","url":null,"abstract":"<div><p><em>Verrucomicrobiota</em><span> is widely distributed in various habitats including insect guts. It was found to be prevalent in almost all investigated termite guts, whereas their physiological functions are not very clear. In this study we characterized the physiological and genomic properties of </span><em>Verrucomicrobiota</em> strain TSB47<sup>T</sup> isolated from <span><em>Reticulitermes</em><em> chinensis</em></span>. The cells of strain TSB47<sup>T</sup><span> were Gram-stain-negative, non-motile, and non-spore-forming coccoid with one or more warts. 16S rRNA gene analysis showed that the closest relatives of strain TSB47</span><sup>T</sup> were <em>Opitutaceae</em> strain TAV1 and <em>Ereboglobus luteus</em> Ho45<sup>T</sup><span> (98.3% and 95.4% sequence similarity, respectively). Whole genome analysis revealed that there are a large number of glycoside hydrolase genes, amino acid metabolism genes, complete Mo-Fe nitrogenase and Fe-Fe nitrogenase gene clusters, as well as </span><em>cbb</em><sub><em>3</em></sub>-type cytochrome oxidase gene in the genome of strain TSB47<sup>T</sup>. Strain TSB47<sup>T</sup> grows well under anaerobic and microaerophilic conditions with a strong tolerance to oxygen. Physiological and genomic characters of strain TSB47<sup>T</sup><span> indicated its high adaptability to termite gut ecosystem. Based on phenotypic and phylogenetic evidence, we suggest strain TSB47</span><sup>T</sup> as the type species of a novel genus in the family <em>Opitutaceae</em>, for which the name <em>Termitidicoccus mucosus</em> sp. nov. is proposed. The type strain is TSB47<sup>T</sup> (CCTCC AB2022447<sup>T</sup>; KCTC 102044<sup>T</sup>).</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"PeriodicalIF":2.6,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139061872","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 ,&nbsp;David Cornu ,&nbsp;Laila Sago ,&nbsp;Virginie Redeker ,&nbsp;Marie-Joelle Virolle","doi":"10.1016/j.resmic.2023.104177","DOIUrl":"10.1016/j.resmic.2023.104177","url":null,"abstract":"<div><p><em>S</em>. <em>lividans</em> and <em>S. coelicolor</em> are phylogenetically closely related strains with different abilities to produce the same specialized metabolites. Previous studies revealed that the strong antibiotic producer, <em>S. coelicolor</em>, had a lower ability to assimilate nitrogen and phosphate than the weak producer, <em>Streptomyces lividans</em>, 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 <em>S. coelicolor</em> than in <em>S. lividans</em> 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 <em>S. coelicolor.</em> Furthermore, in <em>S. lividans</em>, 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.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"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,&nbsp;Annabelle Mathieu-Denoncourt,&nbsp;Marylise Duperthuy","doi":"10.1016/j.resmic.2023.104179","DOIUrl":"10.1016/j.resmic.2023.104179","url":null,"abstract":"<div><p><span><em>Vibrio cholerae</em></span><span><span><span> 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 </span>antimicrobial peptides, including </span>polymyxin B (PmB). In this study, we first investigated the resistance of </span><em>V. cholerae</em><span> 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 </span><em>V. cholerae</em><span> 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.</span></p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"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 ,&nbsp;Isabelle Rincé ,&nbsp;Aurélie Budin-Verneuil ,&nbsp;Cécile Muller ,&nbsp;Josef Deutscher ,&nbsp;Axel Hartke ,&nbsp;Nicolas Sauvageot","doi":"10.1016/j.resmic.2023.104169","DOIUrl":"10.1016/j.resmic.2023.104169","url":null,"abstract":"<div><p><span><em>Enterococcus faecalis</em></span> 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 <em>E. faecalis</em> OG1RF a locus (<em>ega</em>) involved in the catabolism of the glycoamino acid N-acetylglucosamine-L-asparagine. This locus is separated into two transcription units, genes <em>egaRP</em> and <em>egaGBCD1D2</em>, respectively. RT-qPCR experiments revealed that the expression of the <em>ega</em><span> 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 </span><em>ega</em> genes. Growth studies with <em>egaG, egaB and egaC</em> 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-<span>d</span>-glucosaminylamine. The latter can be used as a fermentable carbon source by <em>E. faecalis</em>. Moreover, <span><em>Galleria mellonella</em></span><span> larvae had a significantly higher survival rate when infected with </span><em>ega</em> mutants compared to the wild-type strain, suggesting that the loss of N-acetylglucosamine-L-asparagine utilization affects enterococcal virulence.</p></div>","PeriodicalId":21098,"journal":{"name":"Research in microbiology","volume":null,"pages":null},"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
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信