Whole-genome insights into a multidrug-resistant, biofilm-forming, and pathogenic Salmonella Umbilo isolate and molecular characterization of rare Salmonella serovars from poultry.

IF 4.5 1区 农林科学 Q1 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Seyyide Sarıçam İnce, Akın Ünal, Mehmet Akan
{"title":"Whole-genome insights into a multidrug-resistant, biofilm-forming, and pathogenic Salmonella Umbilo isolate and molecular characterization of rare Salmonella serovars from poultry.","authors":"Seyyide Sarıçam İnce, Akın Ünal, Mehmet Akan","doi":"10.1016/j.psj.2026.107930","DOIUrl":null,"url":null,"abstract":"<p><p>Salmonellosis is one of the leading foodborne zoonoses worldwide, with contaminated poultry products representing a major source of human infection. This study characterized rare Salmonella serovars circulating in poultry flocks with respect to biofilm formation, virulence, antimicrobial resistance (AMR), CRISPR loci diversity, and genomic features. Salmonella isolates were conventionally isolated from drug swap samples and serotyped. Biofilm- (csgA, csgB, csgD, ompR, adrA, rpoS, and fimH) and virulence-associated genes (sipA, sipD, sopB, sopD, sopE, sopE2, sitC, sifA, ssaR, spvC, and pefA) were investigated. CRISPR loci and phenotypic AMR were examined. The Salmonella isolate, which exhibited the highest MAR index, was analyzed by whole-genome sequencing (WGS). Bioinformatic analyses were conducted to determine its plasmid, AMR, and virulence capacity. Thirty rare Salmonella serovars were identified including, Aba, Atento, Ball, Blegdam, Bonariensis, Bradford, Chandans, Fallowfield, Ferruch, Idikan, II (1,9,12:g,m,s,t:e,n,x), Inganda, Korbol, Leeuwarden, Menden, Naestved, Ohlstedt, Papuana, Petahtikve, Sandow, Schwarzengrund, Svedvi, Telaviv, Thompson, Tinda, Tsevie, Tumodi, Umbilo, Uppsala, and Vejle. CsgA-B-C (100.0%) and sipA (96.7%) were the most prevalent genes. S. Sandow harbored all examined genes. CRISPR2 locus (23.3%) was more prevalent than the CRISPR1 locus (3.3%). Resistance to streptomycin (56.7%) and sulfonamides (46.7%) was most common, whereas 40.0% of the isolates were MDR. WGS of the S. Umbilo isolate, which exhibited the highest MAR index (0.48), identified the IncHI2A plasmid (a key factor in horizontal transfer of AMR genes), 12 AMR genes (responsible for resistance to beta-lactams, aminoglycosides, phenicols, and lincosamides), and 181 virulence-associated genes (involved in adhesion, invasion, chemotaxis, intracellular survival, and environmental persistence). The detection of highly resistant and potentially pathogenic S. Umbilo, previously linked to a multinational foodborne outbreak in Europe, highlights its potential public health significance. MLST further proved useful for serovar prediction, with ST2014. Rare Salmonella serovars circulating in poultry flocks possess substantial virulence, biofilm-forming, and AMR potential. These findings highlight the importance of including rare serovars in surveillance and control programs to mitigate foodborne transmission and the spread of AMR.</p>","PeriodicalId":20459,"journal":{"name":"Poultry Science","volume":"105 12","pages":"107930"},"PeriodicalIF":4.5000,"publicationDate":"2026-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13677769/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poultry Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1016/j.psj.2026.107930","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

Salmonellosis is one of the leading foodborne zoonoses worldwide, with contaminated poultry products representing a major source of human infection. This study characterized rare Salmonella serovars circulating in poultry flocks with respect to biofilm formation, virulence, antimicrobial resistance (AMR), CRISPR loci diversity, and genomic features. Salmonella isolates were conventionally isolated from drug swap samples and serotyped. Biofilm- (csgA, csgB, csgD, ompR, adrA, rpoS, and fimH) and virulence-associated genes (sipA, sipD, sopB, sopD, sopE, sopE2, sitC, sifA, ssaR, spvC, and pefA) were investigated. CRISPR loci and phenotypic AMR were examined. The Salmonella isolate, which exhibited the highest MAR index, was analyzed by whole-genome sequencing (WGS). Bioinformatic analyses were conducted to determine its plasmid, AMR, and virulence capacity. Thirty rare Salmonella serovars were identified including, Aba, Atento, Ball, Blegdam, Bonariensis, Bradford, Chandans, Fallowfield, Ferruch, Idikan, II (1,9,12:g,m,s,t:e,n,x), Inganda, Korbol, Leeuwarden, Menden, Naestved, Ohlstedt, Papuana, Petahtikve, Sandow, Schwarzengrund, Svedvi, Telaviv, Thompson, Tinda, Tsevie, Tumodi, Umbilo, Uppsala, and Vejle. CsgA-B-C (100.0%) and sipA (96.7%) were the most prevalent genes. S. Sandow harbored all examined genes. CRISPR2 locus (23.3%) was more prevalent than the CRISPR1 locus (3.3%). Resistance to streptomycin (56.7%) and sulfonamides (46.7%) was most common, whereas 40.0% of the isolates were MDR. WGS of the S. Umbilo isolate, which exhibited the highest MAR index (0.48), identified the IncHI2A plasmid (a key factor in horizontal transfer of AMR genes), 12 AMR genes (responsible for resistance to beta-lactams, aminoglycosides, phenicols, and lincosamides), and 181 virulence-associated genes (involved in adhesion, invasion, chemotaxis, intracellular survival, and environmental persistence). The detection of highly resistant and potentially pathogenic S. Umbilo, previously linked to a multinational foodborne outbreak in Europe, highlights its potential public health significance. MLST further proved useful for serovar prediction, with ST2014. Rare Salmonella serovars circulating in poultry flocks possess substantial virulence, biofilm-forming, and AMR potential. These findings highlight the importance of including rare serovars in surveillance and control programs to mitigate foodborne transmission and the spread of AMR.

多药耐药、生物膜形成和致病性沙门氏菌脐带分离物的全基因组研究以及家禽中罕见沙门氏菌血清型的分子表征。
沙门氏菌病是世界范围内主要的食源性人畜共患病之一,受污染的家禽产品是人类感染的主要来源。本研究从生物膜形成、毒力、抗菌素耐药性(AMR)、CRISPR位点多样性和基因组特征等方面对禽群中罕见的沙门氏菌血清型进行了研究。沙门氏菌分离物通常是从药物交换样本中分离出来并进行血清分型。研究了生物膜- (csgA、csgB、csgD、ompR、adrA、rpoS和fimH)和毒力相关基因(sipA、sipD、sopB、sopD、sopE、sopE2、sitC、sifA、ssaR、spvC和pefA)。检测CRISPR基因座和表型AMR。采用全基因组测序(WGS)对MAR指数最高的沙门氏菌分离物进行了分析。生物信息学分析确定其质粒、抗菌素耐药性和毒力。鉴定出30种罕见的沙门氏菌血清型,包括Aba、Atento、Ball、bllegdam、Bonariensis、Bradford、Chandans、Fallowfield、Ferruch、Idikan、II(1,9、12:g、m、s、t:e、n、x)、Inganda、Korbol、Leeuwarden、Menden、Naestved、Ohlstedt、Papuana、Petahtikve、Sandow、Schwarzengrund、Svedvi、Telaviv、Thompson、Tinda、Tsevie、Tumodi、Umbilo、Uppsala和Vejle。CsgA-B-C(100.0%)和sipA(96.7%)是最常见的基因。S. Sandow携带了所有检测过的基因。CRISPR2位点(23.3%)比CRISPR1位点(3.3%)更普遍。以链霉素(56.7%)和磺胺类药物(46.7%)耐药最为常见,40.0%为耐多药。在MAR指数最高(0.48)的S.脐分离物的WGS中,鉴定出了IncHI2A质粒(AMR基因水平转移的关键因素)、12个AMR基因(负责对β -内酰胺类、氨基糖苷类、酚类和林肯胺类的抗性)和181个毒力相关基因(涉及粘附、侵袭、趋化性、细胞内存活和环境持久性)。高度耐药和潜在致病性的脐带沙门氏菌的发现,以前与欧洲的一次多国食源性疫情有关,突出了其潜在的公共卫生意义。通过ST2014, MLST进一步被证明对血清型预测有用。在家禽群中传播的罕见沙门氏菌血清型具有很强的毒力、生物膜形成和抗菌素耐药性潜力。这些发现突出了将罕见血清型纳入监测和控制规划以减轻食源性传播和抗生素耐药性蔓延的重要性。
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
Poultry Science
Poultry Science 农林科学-奶制品与动物科学
CiteScore
7.60
自引率
15.90%
发文量
0
审稿时长
94 days
期刊介绍: First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers. An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.
×
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
小红书