» Articles » PMID: 31658662

Comparative Analysis of Aerotolerance, Antibiotic Resistance, and Virulence Gene Prevalence in Isolates from Retail Raw Chicken and Duck Meat in South Korea

Overview
Journal Microorganisms
Specialty Microbiology
Date 2019 Oct 30
PMID 31658662
Citations 22
Authors
Affiliations
Soon will be listed here.
Abstract

Human infections with are primarily associated with the consumption of contaminated poultry meat. In this study, we isolated from retail raw chicken and duck meat in Korea and compared their aerotolerance, antibiotic resistance, and virulence gene prevalence. Whereas isolates from chicken dominantly belonged to multilocus sequence typing (MLST) clonal complex (CC)-21, CC-45 is the common MLST sequence type in duck meat isolates. strains from both chicken and duck meat were highly tolerant to aerobic stress. The prevalence of virulence genes was higher in strains from chicken than those from duck meat. However, antibiotic resistance was higher in duck meat isolates than chicken isolates. Based on the prevalence of virulence genes and antibiotic resistance, fluoroquinolone-resistant strains harboring all tested virulence genes except B11 were predominant on retail poultry. Fluoroquinolone-resistant strains carrying most virulence genes were more frequently isolated in summer than in winter. The comparative profiling analysis in this study successfully demonstrated that antibiotic-resistant and pathogenic strains of are highly prevalent on retail poultry and that retail duck meat is an important vehicle potentially transmitting to humans in Korea.

Citing Articles

Comprehensive analysis of antimicrobial resistance dynamics among broiler and duck intensive production systems.

Szoke Z, Fauszt P, Mikolas M, David P, Szilagyi-Tolnai E, Pesti-Asboth G Sci Rep. 2025; 15(1):4673.

PMID: 39920217 PMC: 11806100. DOI: 10.1038/s41598-025-89432-z.


Aerotolerancy of spp.: A Comprehensive Review.

Delaporte E, Karki A, Fakhr M Pathogens. 2024; 13(10).

PMID: 39452714 PMC: 11510350. DOI: 10.3390/pathogens13100842.


A Decade of Antimicrobial Resistance in Human and Animal spp. Isolates.

Barata R, Saavedra M, Almeida G Antibiotics (Basel). 2024; 13(9).

PMID: 39335077 PMC: 11429304. DOI: 10.3390/antibiotics13090904.


Pathogenic Bacteria in Free-Living Birds, and Its Public Health Significance.

Kobuszewska A, Wysok B Animals (Basel). 2024; 14(6).

PMID: 38540066 PMC: 10967383. DOI: 10.3390/ani14060968.


Effect of biofilm formation in a hostile oxidative stress environment on the survival of recovered from poultry in Iraqi markets.

Kanaan M Vet World. 2024; 17(1):136-142.

PMID: 38406363 PMC: 10884572. DOI: 10.14202/vetworld.2024.136-142.


References
1.
Lara-Tejero M, Galan J . A bacterial toxin that controls cell cycle progression as a deoxyribonuclease I-like protein. Science. 2000; 290(5490):354-7. DOI: 10.1126/science.290.5490.354. View

2.
Bolton F, Coates D . A study of the oxygen and carbon dioxide requirements of thermophilic campylobacters. J Clin Pathol. 1983; 36(7):829-34. PMC: 498399. DOI: 10.1136/jcp.36.7.829. View

3.
Rodrigues R, Pocheron A, Hernould M, Haddad N, Tresse O, Cappelier J . Description of Campylobacter jejuni Bf, an atypical aero-tolerant strain. Gut Pathog. 2015; 7:30. PMC: 4653858. DOI: 10.1186/s13099-015-0077-x. View

4.
Adzitey F, Rusul G, Huda N, Cogan T, Corry J . Prevalence, antibiotic resistance and RAPD typing of Campylobacter species isolated from ducks, their rearing and processing environments in Penang, Malaysia. Int J Food Microbiol. 2012; 154(3):197-205. DOI: 10.1016/j.ijfoodmicro.2012.01.006. View

5.
Luangtongkum T, Jeon B, Han J, Plummer P, Logue C, Zhang Q . Antibiotic resistance in Campylobacter: emergence, transmission and persistence. Future Microbiol. 2009; 4(2):189-200. PMC: 2691575. DOI: 10.2217/17460913.4.2.189. View