灵长类分离的支气管杆菌的遗传多样性。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2025-06-26 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1571660
Tracy L Nicholson, Sarah M Shore, Yihui Wang, Lindsey Zimmerman, Tod J Merkel
{"title":"灵长类分离的支气管杆菌的遗传多样性。","authors":"Tracy L Nicholson, Sarah M Shore, Yihui Wang, Lindsey Zimmerman, Tod J Merkel","doi":"10.3389/fmicb.2025.1571660","DOIUrl":null,"url":null,"abstract":"<p><p><i>Bordetella bronchiseptica</i> is a highly contagious bacterial respiratory pathogen with a broad host range of wild and domesticated mammals that can cause a variety of clinical disease outcomes ranging from asymptomatic carriage to severe pneumonia. The goal of this study was to evaluate the genetic diversity of <i>B. bronchiseptica</i> isolates obtained from primates and evaluate the antimicrobial resistance harbored by these isolates. Two isolates were identified as belonging to <i>B. bronchiseptica</i> lineage II and 13 isolates represented new sequence types within <i>B. bronchiseptica</i> lineage I clonal complex 6. The lineage II isolates harbored the lowest sequence identity observed across all genes evaluated and did not contain several well characterized virulence and fimbrial genes. Western blotting revealed no reactivity to a lineage II strain when using antibodies generated against pertactin (PRN) from a lineage I-1 strain or antibodies generated against a domain of filamentous haemagglutinin (FHA) from a lineage I-1 strain. Isolates harbored variation within the <i>wbm</i> locus containing genes encoding for the expression of antigenically distinct O-antigen types and the <i>cya</i> operon was replaced by the <i>ptp</i> operon in several isolates, expanding the phylogenetic distribution of this operon replacement. Thirteen isolates exhibited phenotypic resistance to four antibiotic classes tested, however the <i>Bordetella</i>-specific β-lactamase was the only antimicrobial resistance gene identified. Collectively, the data in this report expands the known phylogenetic diversity and genetic variation of <i>B. bronchiseptica</i> isolates.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":"16 ","pages":"1571660"},"PeriodicalIF":4.0000,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12243275/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genetic diversity of <i>Bordetella bronchiseptica</i> isolates obtained from primates.\",\"authors\":\"Tracy L Nicholson, Sarah M Shore, Yihui Wang, Lindsey Zimmerman, Tod J Merkel\",\"doi\":\"10.3389/fmicb.2025.1571660\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Bordetella bronchiseptica</i> is a highly contagious bacterial respiratory pathogen with a broad host range of wild and domesticated mammals that can cause a variety of clinical disease outcomes ranging from asymptomatic carriage to severe pneumonia. The goal of this study was to evaluate the genetic diversity of <i>B. bronchiseptica</i> isolates obtained from primates and evaluate the antimicrobial resistance harbored by these isolates. Two isolates were identified as belonging to <i>B. bronchiseptica</i> lineage II and 13 isolates represented new sequence types within <i>B. bronchiseptica</i> lineage I clonal complex 6. The lineage II isolates harbored the lowest sequence identity observed across all genes evaluated and did not contain several well characterized virulence and fimbrial genes. Western blotting revealed no reactivity to a lineage II strain when using antibodies generated against pertactin (PRN) from a lineage I-1 strain or antibodies generated against a domain of filamentous haemagglutinin (FHA) from a lineage I-1 strain. Isolates harbored variation within the <i>wbm</i> locus containing genes encoding for the expression of antigenically distinct O-antigen types and the <i>cya</i> operon was replaced by the <i>ptp</i> operon in several isolates, expanding the phylogenetic distribution of this operon replacement. Thirteen isolates exhibited phenotypic resistance to four antibiotic classes tested, however the <i>Bordetella</i>-specific β-lactamase was the only antimicrobial resistance gene identified. Collectively, the data in this report expands the known phylogenetic diversity and genetic variation of <i>B. bronchiseptica</i> isolates.</p>\",\"PeriodicalId\":12466,\"journal\":{\"name\":\"Frontiers in Microbiology\",\"volume\":\"16 \",\"pages\":\"1571660\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-06-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12243275/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3389/fmicb.2025.1571660\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmicb.2025.1571660","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

支气管脓毒杆菌是一种高度传染性的细菌性呼吸道病原体,广泛存在于野生和家养哺乳动物宿主中,可导致从无症状携带到严重肺炎等多种临床疾病结果。本研究的目的是评估从灵长类动物中获得的支杆菌分离株的遗传多样性,并评估这些分离株所携带的抗生素耐药性。2株分离株为分枝杆菌ⅱ系,13株分离株为分枝杆菌ⅰ系克隆复合体6的新序列类型。谱系II分离物在所有被评估的基因中具有最低的序列同一性,并且不包含几个具有良好特征的毒力和菌毛基因。Western blotting显示,当使用来自谱系I-1株的抗peractn (PRN)抗体或来自谱系I-1株的抗丝状血凝素(FHA)结构域的抗体时,对谱系II株无反应性。在含有编码抗原特异性o抗原表达的基因的wbm位点中,分离株存在变异,并且在一些分离株中,cya操纵子被ptp操纵子取代,扩大了这种操纵子替换的系统发育分布。13株菌株对4种抗生素表现出表型抗性,但鉴定出的唯一耐药基因是博德特拉特有的β-内酰胺酶。总的来说,本报告中的数据扩展了已知的支杆菌分离株的系统发育多样性和遗传变异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic diversity of Bordetella bronchiseptica isolates obtained from primates.

Bordetella bronchiseptica is a highly contagious bacterial respiratory pathogen with a broad host range of wild and domesticated mammals that can cause a variety of clinical disease outcomes ranging from asymptomatic carriage to severe pneumonia. The goal of this study was to evaluate the genetic diversity of B. bronchiseptica isolates obtained from primates and evaluate the antimicrobial resistance harbored by these isolates. Two isolates were identified as belonging to B. bronchiseptica lineage II and 13 isolates represented new sequence types within B. bronchiseptica lineage I clonal complex 6. The lineage II isolates harbored the lowest sequence identity observed across all genes evaluated and did not contain several well characterized virulence and fimbrial genes. Western blotting revealed no reactivity to a lineage II strain when using antibodies generated against pertactin (PRN) from a lineage I-1 strain or antibodies generated against a domain of filamentous haemagglutinin (FHA) from a lineage I-1 strain. Isolates harbored variation within the wbm locus containing genes encoding for the expression of antigenically distinct O-antigen types and the cya operon was replaced by the ptp operon in several isolates, expanding the phylogenetic distribution of this operon replacement. Thirteen isolates exhibited phenotypic resistance to four antibiotic classes tested, however the Bordetella-specific β-lactamase was the only antimicrobial resistance gene identified. Collectively, the data in this report expands the known phylogenetic diversity and genetic variation of B. bronchiseptica isolates.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
×
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×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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:604180095
Book学术官方微信