Revisiting the gene loss of respiratory requirements for Salmonella Typhimurium and Salmonella Enteritidis in the chicken infection model.

IF 1.9 4区 生物学 Q3 MICROBIOLOGY
Brazilian Journal of Microbiology Pub Date : 2025-09-01 Epub Date: 2025-05-09 DOI:10.1007/s42770-025-01683-0
Daniel F M Monte, Mauro de Mesquita Souza Saraiva, Julia Memrava Cabrera, Adriana Maria de Almeida, Jacqueline Boldrin de Paiva, Lauanda Monteriro Muniz, Tulio Spina de Lima, Oliveiro Caetano de Freitas Neto, Paul A Barrow, Angelo Berchieri Junior
{"title":"Revisiting the gene loss of respiratory requirements for Salmonella Typhimurium and Salmonella Enteritidis in the chicken infection model.","authors":"Daniel F M Monte, Mauro de Mesquita Souza Saraiva, Julia Memrava Cabrera, Adriana Maria de Almeida, Jacqueline Boldrin de Paiva, Lauanda Monteriro Muniz, Tulio Spina de Lima, Oliveiro Caetano de Freitas Neto, Paul A Barrow, Angelo Berchieri Junior","doi":"10.1007/s42770-025-01683-0","DOIUrl":null,"url":null,"abstract":"<p><p>Salmonella strains are able to use tetrathionate as a terminal respiratory electron acceptor. Here we report the role of ttrRSBCA operon in Salmonella-challenged broilers. Signature-tagged mutagenesis was used to construct defective strains of S. Typhimurium and S. Enteritidis carrying deletions in the whole ttr operon (ΔttrRSBCA) followed by measurement of faecal shedding and cecal colonization counts. Regarding fecal excretion, S. Typhimurium mutant strain harbouring deletion in ttrRSBCA were excreted in similar numbers than the parental wild-type strain during the experimental period, while the SEΔttrRSBCA strain was excreted slightly less in comparison to the wild-type strain. Furthermore, our findings revealed partial attenuation of STMΔttrRSBCA at 2, 5, 7, and 28 days post-infection (dpi), whereas the SEΔttrRSBCA strain was recovered in lower numbers compared to the parental strain at 5, 14, and 28 dpi. These results indicate that such mutations must be accompanied by other genetic changes to obtain a complete attenuation.</p>","PeriodicalId":9090,"journal":{"name":"Brazilian Journal of Microbiology","volume":" ","pages":"2263-2268"},"PeriodicalIF":1.9000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12350878/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brazilian Journal of Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s42770-025-01683-0","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/9 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Salmonella strains are able to use tetrathionate as a terminal respiratory electron acceptor. Here we report the role of ttrRSBCA operon in Salmonella-challenged broilers. Signature-tagged mutagenesis was used to construct defective strains of S. Typhimurium and S. Enteritidis carrying deletions in the whole ttr operon (ΔttrRSBCA) followed by measurement of faecal shedding and cecal colonization counts. Regarding fecal excretion, S. Typhimurium mutant strain harbouring deletion in ttrRSBCA were excreted in similar numbers than the parental wild-type strain during the experimental period, while the SEΔttrRSBCA strain was excreted slightly less in comparison to the wild-type strain. Furthermore, our findings revealed partial attenuation of STMΔttrRSBCA at 2, 5, 7, and 28 days post-infection (dpi), whereas the SEΔttrRSBCA strain was recovered in lower numbers compared to the parental strain at 5, 14, and 28 dpi. These results indicate that such mutations must be accompanied by other genetic changes to obtain a complete attenuation.

在鸡感染模型中鼠伤寒沙门菌和肠炎沙门菌呼吸需求基因缺失的研究。
沙门氏菌菌株能够使用四硫酸盐作为终端呼吸电子受体。在这里,我们报告了ttrRSBCA操纵子在沙门氏菌攻击肉鸡中的作用。采用特征标记诱变技术构建鼠伤寒沙门氏菌和肠炎沙门氏菌携带整个ttr操纵子缺失的缺陷菌株(ΔttrRSBCA),然后测量粪便脱落和盲肠定植计数。在粪便排泄方面,携带ttrRSBCA缺失的鼠伤寒沙门氏菌突变株在实验期间的排泄量与亲本野生型菌株相似,而SEΔttrRSBCA菌株的排泄量略低于野生型菌株。此外,我们的研究结果显示STMΔttrRSBCA在感染后2、5、7和28天(dpi)部分衰减,而SEΔttrRSBCA菌株在感染后5、14和28天恢复的数量比亲本菌株要少。这些结果表明,这种突变必须伴随着其他遗传变化才能获得完全衰减。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Brazilian Journal of Microbiology
Brazilian Journal of Microbiology 生物-微生物学
CiteScore
4.10
自引率
4.50%
发文量
216
审稿时长
1.0 months
期刊介绍: The Brazilian Journal of Microbiology is an international peer reviewed journal that covers a wide-range of research on fundamental and applied aspects of microbiology. The journal considers for publication original research articles, short communications, reviews, and letters to the editor, that may be submitted to the following sections: Biotechnology and Industrial Microbiology, Food Microbiology, Bacterial and Fungal Pathogenesis, Clinical Microbiology, Environmental Microbiology, Veterinary Microbiology, Fungal and Bacterial Physiology, Bacterial, Fungal and Virus Molecular Biology, Education in Microbiology. For more details on each section, please check out the instructions for authors. The journal is the official publication of the Brazilian Society of Microbiology and currently publishes 4 issues per year.
×
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