Prevalence, main serovars and anti-microbial resistance profiles of non-typhoidal Salmonella in poultry samples from the Americas: A systematic review and meta-analysis
- PMID: 34724337
- DOI: 10.1111/tbed.14362
Prevalence, main serovars and anti-microbial resistance profiles of non-typhoidal Salmonella in poultry samples from the Americas: A systematic review and meta-analysis
Abstract
Poultry and poultry-derived products such as meat and eggs are among the main sources of non-typhoidal Salmonella (NTS) transmission to humans. Therefore, we performed a systematic review and used random-effects meta-analyses to (1) estimate the prevalence of NTS in poultry samples from birds, products and subproducts and environmental samples, (2) examine the diversity and frequency of their serovars and (3) estimate the prevalence and profiles of anti-microbial resistance (AMR) in NTS isolates reported in studies from the Americas. We included 157 studies from 15 countries comprising 261,408 poultry samples and estimated an overall pooled prevalence of 17.9% (95% Confidence Interval: 10.8-26.3) in birds, 21.8% (17.7-26.1) in products and subproducts and 29.5% (24.2-35.1) in environmental samples. At the national level, the prevalence of NTS was heterogeneous across countries with the highest values in Mexico, the United States and Canada. In total, 131 serovars were identified from 13,388 isolates; Heidelberg, Kentucky, Enteritidis and Typhimurium were the most prevalent in the overall top 10 ranking (range 6.5%-20.8%). At the national level, Enteritidis and Typhimurium were identified in most of the countries, though with national differences in their ranks. The prevalence of AMR increased from 24.1% for 1 antibiotic to 36.2% for 2-3 antibiotics and 49.6% for ≥ 4 antibiotics. Kentucky, Heidelberg, Typhimurium and Enteritidis were the serovars with the highest prevalence of AMR. Besides, tetracycline, ampicillin, streptomycin, ceftiofur and amoxicillin-clavulanic acid were the most frequent antibiotics to which NTS showed resistance. In conclusion, NTS was distributed through the avian production chain with high and heterogeneous values of prevalence in poultry samples. Besides, there were distinctive patterns of serovars distribution across countries and an alarming prevalence of AMR among zoonotic serovars.
Keywords: anti-microbial resistance; non-typhoid Salmonella; poultry; prevalence; serotyping.
© 2021 Wiley-VCH GmbH.
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References
REFERENCES
-
- Andino, A., & Hanning, I. (2015). Salmonella enterica: Survival, colonization, and virulence differences among serovars. Scientific World Journal, 2015, 520179. https://doi.org/10.1155/2015/520179
-
- Antonelli, P., Belluco, S., Mancin, M., Losasso, C., & Ricci, A. (2019). Genes conferring resistance to critically important antimicrobials in Salmonella enterica isolated from animals and food: A systematic review of the literature, 2013-2017. Research in Veterinary Science, 126, 59-67. https://doi.org/10.1016/j.rvsc.2019.08.022
-
- Antunes, P., Mourão, J., Campos, J., & Peixe, L. (2016). Salmonellosis: The role of poultry meat. Clinical Microbiology and Infection, 22(2), 110-121. https://doi.org/10.1016/j.cmi.2015.12.004
-
- Barrow, P. A., Jones, M. A., Smith, A. L., & Wigley, P. (2012). The long view: Salmonella-the last forty years. Avian Pathology, 41(5), 413-420. https://doi.org/10.1080/03079457.2012.718071
-
- Barrow, P., & Methner, U. (Eds.) (2013). Salmonella in domestic animals. (2nd ed.). CABI.
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