» Articles » PMID: 31057528

Antimicrobial Resistance Genes, Cassettes, and Plasmids Present in Associated With United States Food Animals

Abstract

The ability of antimicrobial resistance (AR) to transfer, on mobile genetic elements (MGEs) between bacteria, can cause the rapid establishment of multidrug resistance (MDR) in bacteria from animals, thus creating a foodborne risk to human health. To investigate MDR and its association with plasmids in , whole genome sequence (WGS) analysis was performed on 193 isolated from sources associated with United States food animals between 1998 and 2011; 119 were resistant to at least one antibiotic tested. Isolates represented 86 serotypes and variants, as well as diverse phenotypic resistance profiles. A total of 923 AR genes and 212 plasmids were identified among the 193 strains. Every isolate contained at least one AR gene. At least one plasmid was detected in 157 isolates. Genes were identified for resistance to aminoglycosides ( = 472), β-lactams ( = 84), tetracyclines ( = 171), sulfonamides ( = 91), phenicols ( = 42), trimethoprim ( = 8), macrolides ( = 5), fosfomycin ( = 48), and rifampicin ( = 2). Plasmid replicon types detected in the isolates were A/C ( = 32), ColE ( = 76), F ( = 43), HI1 ( = 4), HI2 ( = 20), I1 ( = 62), N ( = 4), Q ( = 7), and X ( = 35). Phenotypic resistance correlated with the AR genes identified in 95.4% of cases. Most AR genes were located on plasmids, with many plasmids harboring multiple AR genes. Six antibiotic resistance cassette structures (ARCs) and one pseudo-cassette were identified. ARCs contained between one and five resistance genes (ARC1: 2, ; ARC2: ; ARC3: ; ARC4: ; ARC5: ; ARC6: ; pseudo-ARC: 1). These ARCs were present in multiple isolates and on plasmids of multiple replicon types. To determine the current distribution and frequency of these ARCs, the public NCBI database was analyzed, including WGS data on isolates collected by the USDA Food Safety and Inspection Service (FSIS) from 2014 to 2018. ARC1, ARC4, and ARC5 were significantly associated with cattle isolates, while ARC6 was significantly associated with chicken isolates. This study revealed that a diverse group of plasmids, carrying AR genes, are responsible for the phenotypic resistance seen in isolated from United States food animals. It was also determined that many plasmids carry similar ARCs.

Citing Articles

Whole-Genome Shotgun Sequencing from Chicken Clinical Tracheal Samples for Bacterial and Novel Bacteriophage Identification.

Chrzastek K, Seal B, Kulkarni A, Kapczynski D Vet Sci. 2025; 12(2).

PMID: 40005922 PMC: 11861695. DOI: 10.3390/vetsci12020162.


Genomic characterization of foodborne Salmonella enterica and Escherichia coli isolates from Saboba district and Bolgatanga Municipality Ghana.

Sunmonu G, Adzitey F, Odih E, Tibile B, Ekli R, Aduah M PLoS One. 2025; 20(2):e0315583.

PMID: 39919045 PMC: 11805442. DOI: 10.1371/journal.pone.0315583.


Defense mechanisms of against antibiotics: a review.

Punchihewage-Don A, Ranaweera P, Parveen S Front Antibiot. 2025; 3():1448796.

PMID: 39816264 PMC: 11731628. DOI: 10.3389/frabi.2024.1448796.


An eco-evolutionary perspective on antimicrobial resistance in the context of One Health.

Bustamante M, Mei S, Daras I, van Doorn G, Falcao Salles J, de Vos M iScience. 2025; 28(1):111534.

PMID: 39801834 PMC: 11719859. DOI: 10.1016/j.isci.2024.111534.


Plasmidome of Salmonella enterica serovar Infantis recovered from surface waters in a major agricultural region for leafy greens in California.

Quinones B, Lee B, Aviles Noriega A, Gorski L PLoS One. 2025; 19(12):e0316466.

PMID: 39775564 PMC: 11684603. DOI: 10.1371/journal.pone.0316466.


References
1.
Magnet S, Courvalin P, Lambert T . Activation of the cryptic aac(6')-Iy aminoglycoside resistance gene of Salmonella by a chromosomal deletion generating a transcriptional fusion. J Bacteriol. 1999; 181(21):6650-5. PMC: 94128. DOI: 10.1128/JB.181.21.6650-6655.1999. View

2.
Carattoli A . Plasmid-mediated antimicrobial resistance in Salmonella enterica. Curr Issues Mol Biol. 2003; 5(4):113-22. View

3.
Frey J, Bagdasarian M, Bagdasarian M . Replication and copy number control of the broad-host-range plasmid RSF1010. Gene. 1992; 113(1):101-6. DOI: 10.1016/0378-1119(92)90675-f. View

4.
Carattoli A, Bertini A, Villa L, Falbo V, Hopkins K, Threlfall E . Identification of plasmids by PCR-based replicon typing. J Microbiol Methods. 2005; 63(3):219-28. DOI: 10.1016/j.mimet.2005.03.018. View

5.
Garcia-Fernandez A, Chiaretto G, Bertini A, Villa L, Fortini D, Ricci A . Multilocus sequence typing of IncI1 plasmids carrying extended-spectrum beta-lactamases in Escherichia coli and Salmonella of human and animal origin. J Antimicrob Chemother. 2008; 61(6):1229-33. DOI: 10.1093/jac/dkn131. View