2016
DOI: 10.1016/j.foodcont.2016.04.026
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Prevalence and serovar diversity of Salmonella spp. in primary horticultural fruit production environments

Abstract: Increases in foodborne disease outbreaks associated with fresh produce have necessitated the need to identify potential sources of microbial contamination in produce and agricultural environments. The present study evaluated Salmonella prevalence and serovar diversity in show the potential of agricultural fruit production environments to act as reservoirs of clinically important Salmonella serovars.

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Cited by 21 publications
(10 citation statements)
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“…Micro‐organisms from all samples ( n = 18) were isolated as previously described by Gomba et al . (), with slight modifications. A 25‐g sample from each vine was placed in a beaker with sterile peptone‐buffered water (PBW) (Biolab, Merck, Johnnesburg, South Africa) supplemented with 0.025% Tween80 (Associated Chemical Enterprises, Johannesburg), sonicated for 5 min in an ultrasonic water bath (Labotec, Johannebsurg) to dislodge microbes from plant surfaces.…”
Section: Methodsmentioning
confidence: 99%
“…Micro‐organisms from all samples ( n = 18) were isolated as previously described by Gomba et al . (), with slight modifications. A 25‐g sample from each vine was placed in a beaker with sterile peptone‐buffered water (PBW) (Biolab, Merck, Johnnesburg, South Africa) supplemented with 0.025% Tween80 (Associated Chemical Enterprises, Johannesburg), sonicated for 5 min in an ultrasonic water bath (Labotec, Johannebsurg) to dislodge microbes from plant surfaces.…”
Section: Methodsmentioning
confidence: 99%
“…Supernatant from macerated fresh produce samples in 0.1% PBW was used to determine presence of total coliforms, E. coli, Enterococci, and Pseudomonas with Colilert-18, Enterolert- For Salmonella detection, macerated baby spinach, lettuce, and cabbage samples were incubated at 37 8C for 24 hrs. Thereafter, 0.1 ml of the pre-enriched culture was inoculated in 10 ml Rappaport-Vassiliadis (Merck) and incubated at 42 8C for 18-24 hrs before plating (0.1 ml) in Xylose Lysine Deoxycholate agar (Merck) (Gomba et al, 2016). Pre-enriched macerated vegetable samples (0.1 ml) were also enriched to detect the presence of L. monocytogenes using 10 ml Listeria enrichment broth, incubated at 37 8C for 18-24 hrs and then plated on Listeria agar (Merck).…”
Section: Microbiological and Pathogen Analyses 221 | Leafy Green mentioning
confidence: 99%
“…For instance, this procedure can be applied to identify Salmonella spp. (104,107) and for the detection of plasmid insertion in E. coli. (108) It has also been used to discriminate wild-type isolates from ampicillin-resistant E. coli.…”
Section: Matric Assisted Laser Desorption Ionization Time Of Flight (mentioning
confidence: 99%