Mapping Integron-Associated AMR Genes in Whole Genome Sequences of <i>Salmonella</i> Typhimurium from Dairy Cattle
<b>Background:</b> Antimicrobial resistance (AMR) is a critical global health threat, with AMR <i>Salmonella enterica</i> serovar Typhimurium strains being a major foodborne pathogen. Integrons, a type of mobile genetic element, capture and transfer resistance genes, thereby...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-06-01
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| Series: | Antibiotics |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2079-6382/14/7/633 |
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| Summary: | <b>Background:</b> Antimicrobial resistance (AMR) is a critical global health threat, with AMR <i>Salmonella enterica</i> serovar Typhimurium strains being a major foodborne pathogen. Integrons, a type of mobile genetic element, capture and transfer resistance genes, thereby playing a role in the spread of AMR. <b>Objectives:</b> This study aimed to characterize the locations of integrons carrying AMR genes within the whole genomes of 32 <i>Salmonella</i> Typhimurium isolates collected from dairy cattle by two U.S. Veterinary Diagnostic Laboratories between 2009 and 2012. <b>Methods:</b> Class I integrons were sequenced from PCR-amplified products. DNA was extracted, quantified, barcoded, and sequenced on the Illumina MiSeq platform. Whole genome sequences were trimmed and assembled using the SPAdes assembler in Geneious Prime<sup>®</sup>, and plasmids were identified with the PlasmidFinder pipeline in Linux. Integron locations were determined by aligning their sequences with whole genome contigs and plasmids, while AMR genes were identified through BLAST with the MEGARes 3.0 database and confirmed by alignment with isolate, plasmid, and integron sequences. Statistical analysis was applied to compare the proportions of isolates harboring integrons on their chromosome versus plasmids and also to examine the associations between integron presence and AMR gene presence. <b>Results:</b> Seven plasmid types were identified from all isolates: IncFII(S) (n = 14), IncFIB(S) (n = 13), IncC (n = 7), Inc1-I(Alpha) (n = 3), and ColpVC, Col(pAHAD28), and Col8282 (1 isolate each). Of the 32 isolates, 16 (50%) carried at least one size of integron. Twelve of them carried both 1000 and 1200 bp; 3 carried only 1000 bp and 1 carried 1800 bp integrons. Of the 15 isolates that carried 1000 bp integron, 12 harbored it on IncFIB(S) plasmids, 2 on IncC plasmids, and 1 on the chromosome. The 1200 bp integrons from all 12 isolates were located on chromosomes. There were significant positive associations between the presence of integrons and the presence of several AMR genes including <i>sul1</i>, <i>aadA2</i>, <i>blaCARB-2</i>, <i>qacEdelta1</i>, <i>tet(G),</i> and <i>floR</i> (<i>p</i> < 0.05). AMR genes were located as follows: <i>aadA2</i> on IncFIB(S) and IncC plasmids; <i>bla<sub>CMY-2</sub></i> on IncC plasmid; <i>qacEdelta1</i> on IncFIB(S), IncC, and chromosome; <i>bla<sub>CARB-2</sub></i>, <i>floR</i>, <i>tet(A)</i> and <i>tet(G)</i> on the chromosome. <b>Conclusions:</b> The findings highlight the genomic and plasmid complexity of <i>Salmonella</i> Typhimurium which is impacted by the presence and location of integrons, and this study provides genomic insights that can inform efforts to enhance food safety and protect both animal and public health. |
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| ISSN: | 2079-6382 |