Evidence map›Paper›PMID 41904466›Full record

ArticleBMC veterinary research2026

Convergence of multidrug resistance, virulence, and biofilm formation in Salmonella isolates from humans, animals, and food in Xinjiang, China.

Xueqin Lan, Houhong Wang, Kaiqi Ma, Yixin Bai, Qirui Zang, Ying Huang, Wanjing Jin, Meiling Wang, Zhanqiang Su, Mengfei Zhang and 3 more

Abstract read
In one paragraph

Article in BMC veterinary research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

13 authors.

Xueqin Lan *College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Houhong Wang *Disease Prevention and Control Center of Midong District (Health Supervision Institute), Urumqi, China.
Kaiqi MaFukang Vocational and Technical College, Fukang, China.
Yixin BaiCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Qirui ZangCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Ying HuangCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Wanjing JinCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Meiling WangCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Zhanqiang SuCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Mengfei ZhangCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Gulina AishanIli Kazakh Autonomous Prefecture General Animal Husbandry Station, Yining, Xinjiang Uighur Autonomous Region, China.
Jinxin XieCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China.
Panpan TongCollege of Veterinary Medicine, Xinjiang Agricultural University, Urumqi, China. tongpanpan123@163.com.

Funding

Technology Action Project for Rural Revitalization Industry Development in Xinjiang Uygur Autonomous Region 2024NC034
6 · The paper itself

Abstract

backgroundSalmonella, a major Gram-negative enterobacterial pathogen, is a leading cause of foodborne illnesses worldwide. This study characterizes Salmonella isolates from human, animal, and food sources in Xinjiang, China, by analyzing their biofilm-forming capacity, antimicrobial resistance (AMR), virulence genes, serotypes, and sequence types based on multilocus sequence types (MLST) analysis.

methodsA total of 1,446 samples, including rectal swabs from poultry, cattle, sheep, and camels, equine abortion tissues, retail chicken samples, and human fecal specimens from outpatients with acute diarrhea, were collected between 2018 and 2025 in Xinjiang, China. Salmonella was isolated using standard culture methods (pre-enrichment in buffered peptone water, selective enrichment in Rappaport-Vassiliadis and tetrathionate broths, and plating on XLT-4 agar) and was confirmed by PCR (polymerase chain reaction) analysis of the invA gene. Biofilm formation was assessed using the crystal violet staining. Antimicrobial susceptibility was determined by disk diffusion following the CLSI guidelines (2020). Whole-genome sequencing was performed on an Illumina NovaSeq 6000 platform, and bioinformatics analysis was used to identify AMR genes (CARD, ≥ 90% identity, ≥ 80% coverage), virulence factors (VFDB, ≥ 90% identity, ≥ 80% coverage), serotypes (SeqSero2), and sequence types (PubMLST).

resultsForty-nine Salmonella isolates (26 from animals, 23 from humans) were obtained after isolation and confirmation of the invA gene. Of these, 91.8% exhibited strong biofilm-forming capacity. High resistance rates were observed for ampicillin (65.3%), streptomycin (59.2%), tetracycline (49.0%), and trimethoprim-sulfamethoxazole (30.6%), with 48.9% classified as multidrug-resistant (MDR). Analysis of resistance genes indicated high frequencies of blaTEM−1 (51.0%), aph(3’’)-Ib (40.8%), aph(6)-Id (40.8%), and tet(A) (38.8%), with strong concordance between genotypes and phenotypes (e.g., blaTEM−1 with ampicillin resistance; aph(3’’)-Ib/aph(6)-Id with streptomycin resistance). Virulence profiling identified approximately 200 unique genes across eight functional classes, with near-universal presence of iron acquisition genes (e.g., fepG; 98.0%), type III secretion system genes (e.g., sipA, sspA, and invA; 95.9%), and fimbrial adhesion genes (e.g., fimH; 91.8%). Serotyping identified S. Enteritidis (26.5%), S. Typhimurium (16.3%), and S. Agona (16.3%) as the most prevalent serotypes, while MLST analysis showed ST11 (28.6%) as the dominant sequence type, primarily within phylogenetic groups B (44.9%) and D1 (26.5%).

conclusionThe co-occurrence of MDR, diverse virulence factors, and strong biofilm-forming capacities in the Salmonella isolates suggests an increased potential for environmental persistence and zoonotic transmission. These findings highlight significant public health risks and provide critical molecular insights to inform targeted surveillance and control strategies for Salmonella in this understudied region.

Indexed as

BiofilmsDrug Resistance, Multiple, BacterialSalmonellaSalmonella InfectionsAnimalsAnti-Bacterial AgentsCattleChinaFood MicrobiologyHumansMicrobial Sensitivity TestsMultilocus Sequence TypingSalmonella Infections, AnimalSheepVirulenceVirulence FactorsAnti-Bacterial AgentsVirulence FactorsAnimal sourcesAntimicrobial resistanceBiofilmFood sourcesHuman clinical isolatesMultilocus sequence typing (MLST)Resistance genesSalmonellaVirulence genes

Identifiers

PMID41904466
PMCPMC13151388

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