Assessment of Virulence Genes and Antibiotic Resistance in Pseudomonas aeruginosa Isolates from Poultry Carcasses

Authors

DOI:

https://doi.org/10.56294/hl2025590

Keywords:

Antibiotic resistance, hemolysin, protease, pseudomonas aeruginosa, carcass surface swab prevalence, virulence factors

Abstract

Pseudomonas aeruginosa, a major human pathogen, poses a significant threat to food, particularly meat products, due to its aggressiveness and drug resistance. Research aims to identify and analyze P. aeruginosa samples from poultry carcasses, examining their antimicrobial resistance and potential pathogenicity patterns. A total of 670 samples of poultry carcasses were gathered from slaughterhouses and shopping centers. Biochemical testing, Polymerase Chain Reaction (PCR) targeted the oprL gene, and culture-based techniques were used to identify the isolates. The virulence factors were identified both genotypically (by PCR amplification of exoS, toxA, and lasB) and phenotypically (by detection of hemolysin, protease, elastase, and biofilm formation). Data analysis was performed using SPSS software (version 26) to evaluate the results and determine associations between antibiotic resistance profiles and phenotypic virulence features. P. aeruginosa was identified from 102 samples (15.2%) out of 670 samples. Protease activity was identified in 69.6% of these isolates, hemolysin synthesis in 76.5%, and biofilm formation in 83.3%. According to PCR data, 58.8% of the isolates had exoS, 51.9% had toxA, and 64.7% had lasB. Ceftazidime (61.7%) and ciprofloxacin (52.9%) showed high resistance, with 48.0% of cases being categorized as multidrug-resistant (MDR). Public health is likely to be at risk due to the presence of virulent, multidrug-resistant Pseudomonas aeruginosa in poultry carcasses, which emphasizes better hygiene management and antimicrobial surveillance in poultry processing.

References

1. Poursina S, Ahmadi M, Fazeli F, Ariaii P. Assessment of virulence factors and antimicrobial resistance among the Pseudomonas aeruginosa strains isolated from animal meat and carcass samples. Veterinary medicine and science. 2023 Jan; 9(1):315-25.https://doi.org/10.1002/vms3.1007

2. Heredia N, García S. Animals as sources of food-borne pathogens: A review. Animal nutrition. 2018 Sep 1; 4(3):250-5.https://doi.org/10.1016/j.aninu.2018.04.006

3. Vijayalakshmi P, RajaniChowdary A, Vidyullatha P, Sushma M. Identification of bacteriological quality and antimicrobial resistance of microorganisms isolated from animal foods collected from the abattoir, butcher shops and local seafood market. Food Research. 2021 Jun;5(3):144-51.https://doi.org/10.26656/fr.2017.5(3).570

4. Elbehiry A, Marzouk E, Aldubaib M, Moussa I, Abalkhail A, Ibrahem M, et al. Pseudomonas species prevalence, protein analysis, and antibiotic resistance: An evolving public health challenge. AMB Express. 2022 Dec; 12(1):1-4.https://doi.org/10.1186/s13568-022-01390-1

5. Jawher IM, Hasan MG. Molecular identification of Pseudomonas aeruginosa in meat at Mosul city retails using PCR technique. Iraqi Journal of Veterinary Sciences. 2022 Oct 1; 36(4):1083-7.https://doi.org/10.33899/ijvs.2022.133086.2173

6. Circella E, Schiavone A, Barrasso R, Camarda A, Pugliese N, Bozzo G. Pseudomonas azotoformans belonging to Pseudomonas fluorescens group as the causative agent of blue coloration in carcasses of slaughterhouse rabbits. Animals. 2020 Feb 6;10(2):256.https://doi.org/10.1002/vms3.1007

7. Łada P, Kończyk-Kmiecik K, Bancerz-Kisiel A. Isolation, characterization and antimicrobial resistance of Yersinia enterocolitica from Polish cattle and their carcasses. BMC veterinary research. 2023 Sep 5; 19(1):143.https://doi.org/10.1186/s12917-023-03700-6

8. Mehmood S, Ali K, Bashir A, Farid N, Fatima K, Naz S.Biorisk. Management and Antibiotic Susceptibility Pattern of Biofilm producing Pseudomonas aeruginosa Isolated from Broiler Chicken: A Public Health Concern: Biorisk Management of Biofilm producing Pseudomonas aeruginosa from Broiler Chicken. Proceedings of the Pakistan Academy of Sciences: B. Life and Environmental Sciences. 2023 Sep 5;60(3):497-503.https://doi.org/10.53560/PPASB(60-3)866

9. Elrais AM, Arab WS, Sallam KI, Elmegid WA, Elgendy F, Elmonir W, et al. Prevalence, Virulence Genes, Phylogenetic Analysis, and Antimicrobial Resistance Profile of Helicobacter Species in Chicken Meat and Their Associated Environment at Retail Shops in Egypt. Foods. 2022 Jun 26;11(13):1890.https://doi.org/10.3390/foods11131890

10. Karim MR, Zakaria Z, Hassan L, MohdFaiz N, Ahmad NI. Antimicrobial Resistance Profiles and Co-Existence of Multiple Antimicrobial Resistance Genes in mcr-HarbouringColistin-Resistant Enterobacteriaceae Isolates Recovered from Poultry and Poultry Meats in Malaysia. Antibiotics. 2023 Jun 15;12(6):1060.https://doi.org/10.3390/antibiotics12061060

11. Okorie-Kanu OJ, Anyanwu MU, Ezenduka EV, Mgbeahuruike AC, Thapaliya D, Gerbig G, et al. Molecular epidemiology, genetic diversity and antimicrobial resistance of Staphylococcus aureus isolated from chicken and pig carcasses, and carcass handlers. PLoS One. 2020 May 14;15(5):e0232913.https://doi.org/10.1371/journal.pone.0232913

12. Radovanovic RS, Savic NR, Ranin L, Smitran A, OpavskiNV,Tepavcevic AM, et al. Biofilm production and antimicrobial resistance of clinical and food isolates of Pseudomonas spp. Current Microbiology. 2020 Dec; 77:4045-52.https://doi.org/10.1007/s00284-020-02236-4

13. TorkiBaghbaderani Z, Shakerian A, Rahimi E. Phenotypic and genotypic assessment of antibiotic resistance of Staphylococcus aureus bacteria isolated from retail meat. Infection and drug resistance. 2020 May 7:1339-49.https://doi.org/10.2147/IDR.S241189

14. Gregova G, Kmet V. Antibiotic resistance and virulence of Escherichia coli strains isolated from animal rendering plant. Scientific reports. 2020 Oct 13;10(1):17108.https://doi.org/10.1038/s41598-020-72851-5

15. Wieczorek K, Bocian Ł, Osek J. Prevalence and antimicrobial resistance of Campylobacter isolated from carcasses of chickens slaughtered in Poland–a retrospective research. Food control. 2020 Jun 1; 112:107159.https://doi.org/10.1016/j.foodcont.2020.107159

16. Laaksonen S, Oksanen A, Julmi J, Zweifel C, Fredriksson-Ahomaa M, Stephan R. Presence of foodborne pathogens, extended-spectrum β-lactamase-producing Enterobacteriaceae, and methicillin-resistant Staphylococcus aureus in slaughtered reindeer in northern Finland and Norway. ActaVeterinariaScandinavica. 2017 Dec;59(1):1-8.https://doi.org/10.1186/s13028-016-0272-x.

Downloads

Published

2025-08-04

How to Cite

1.
N A, Patel K, Garg M, Kaur P, Ramu N, Ray S. Assessment of Virulence Genes and Antibiotic Resistance in Pseudomonas aeruginosa Isolates from Poultry Carcasses. Health Leadership and Quality of Life [Internet]. 2025 Aug. 4 [cited 2025 Aug. 30];4:590. Available from: https://hl.ageditor.ar/index.php/hl/article/view/590