Detection of pathogenic serogroups and virulence genes in Listeria monocytogenes strains isolated from beef and beef products retailed in Gauteng Province, South Africa, using phenotypic and polymerase chain reaction (PCR)-based methods
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Date
Authors
Gana, James
Gcebe, Nomakorinte
Moerane, Rebone
Ngoshe, Yusuf Bitrus
Moabelo, Khomotso C.
Adesiyun, Abiodun Adewale
Journal Title
Journal ISSN
Volume Title
Publisher
Wiley-Hindawi
Abstract
South Africa recently (2017-18) experienced the largest outbreak of human listeriosis in the world caused by L. monocytogenes following the consumption of “polony,” a ready-to-eat meat product. Most (59%) cases originated from Gauteng province, South Africa. As a follow-up study to the outbreak, we used standard bacteriological and molecular methods to determine the prevalence of pathogenic and virulent serogroups of L. monocytogenes in various beef and beef products retailed in Gauteng province, South Africa. The overall prevalence of Listeria spp. was 28% (112/400), comprising Listeria monocytogenes (9.3%), Listeria innocua (16.3%), and Listeria welshimeri (2.5%) (p < 0.001). It is crucial to have detected that the region (p = 0.036), type of product (p = 0.032), and temperature at storage (p = 0.011) significantly affected the occurrence of L. monocytogenes in beef products. It is alarming that pathogenic serogroups 4b-4d-4e (51.4%) and 1/2a-3a (43.2%) were detected among the isolates of L. monocytogenes. Importantly, they were all carriers of seven virulence-associated genes (hlyA, inlB, plcA, iap, inlA, inlC, and inlJ). Our study also demonstrated that 16.7% of “polony” samples investigated were contaminated with L. monocytogenes. Considering that pathogenic and virulent L. monocytogenes contaminated beef and beef products retailed in South Africa, the food safety risk posed to consumers remains and cannot be ignored. Therefore, it is imperative to reduce the contamination of these products with L. monocytogenes during beef production, processing, and retailing to avoid future outbreaks of human listeriosis in the country.
Description
DATA AVAILABILITY : All the data are contained within the article.
SUPPLEMENTARY MATERIALS : Supplementary information includes the number of samples collected across 48 retail outlets and the frequency of detection of L. monocytogenes, L. innocua, and L. welshimeri from beef and beef products sampled from retail outlets, the strategy used for sample collection from classes of retail outlets, the primers used for mPCR speciation, serogrouping, and virulence gene detection in L. monocytogenes isolates. (Supplementary Materials)
SUPPLEMENTARY MATERIALS : Supplementary information includes the number of samples collected across 48 retail outlets and the frequency of detection of L. monocytogenes, L. innocua, and L. welshimeri from beef and beef products sampled from retail outlets, the strategy used for sample collection from classes of retail outlets, the primers used for mPCR speciation, serogrouping, and virulence gene detection in L. monocytogenes isolates. (Supplementary Materials)
Keywords
Listeriosis, Outbreak, Listeria monocytogenes, Gauteng Province, South Africa, Beef products, SDG-02: Zero hunger, SDG-03: Good health and well-being
Sustainable Development Goals
SDG-02:Zero Hunger
SDG-03:Good heatlh and well-being
SDG-03:Good heatlh and well-being
Citation
Gana, J., Gcebe, N., Moerane, R. et al. 2024, 'Detection of pathogenic serogroups and virulence genes in Listeria monocytogenes strains isolated from beef and beef products retailed in Gauteng Province, South Africa, using phenotypic and polymerase chain reaction (PCR)- based methods', International Journal of Microbiology, vol. 2024, art. ID 8891963, pp. pp. 1-11.
https://DOI.org/10.1155/2024/8891963