2019
DOI: 10.3390/pathogens8040191
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Molecular Detection and Antibiotyping of Multidrug-Resistant Salmonella Isolated from Houseflies in a Fish Market

Abstract: Houseflies (Musca domestica) are well-known mechanical vectors for spreading multidrug-resistant bacteria. Fish sold in open markets are exposed to houseflies. The present study investigated the prevalence and antibiotypes of multidrug-resistant (MDR) Salmonella spp. in houseflies captured from a fish market. Direct interviews with fish vendors and consumers were also performed to draw their perceptions about the role of flies in spreading antibiotic-resistant bacteria. A total of 60 houseflies were captured f… Show more

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Cited by 16 publications
(12 citation statements)
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“…Several studies detected the tetA gene in E. coli and Salmonella spp. from dairy farms, boiler farms, house flies, and aquatic environments [31,33,[50][51][52]. However, there were no studies on the detection of the tetA gene in E. coli and Salmonella from turkeys.…”
Section: Discussionmentioning
confidence: 99%
“…Several studies detected the tetA gene in E. coli and Salmonella spp. from dairy farms, boiler farms, house flies, and aquatic environments [31,33,[50][51][52]. However, there were no studies on the detection of the tetA gene in E. coli and Salmonella from turkeys.…”
Section: Discussionmentioning
confidence: 99%
“…Ltd., Mumbai, India) consecutively and were incubated at 42 °C for 24 h. Following enrichment, a loopful of enriched broth was initially streaked on Salmonella–Shigella (SS) agar, and pure colonies (single pinkish with black center) were streaked on xylose–lysine–deoxycholate (XLD) agar (HiMedia Laboratories Pvt. Ltd, Mumbai, India) and plates were incubated at 37 °C for 24 h. Colonies were identified as Salmonella based on morphological and biochemical properties using Gram’s stain, catalase test and indole test as was previously described [ 18 ]. For further confirmation, 4–6 colonies from each sample were tested biochemically by dilution streaking and stabbed onto triple sugar iron (TSI) agar (Merck, Germany) and tubes were incubated at 37 °C for 16–24 h [ 19 ].…”
Section: Methodsmentioning
confidence: 99%
“…The final confirmation of E. coli was done by polymerase chain reaction (PCR) assays targeting the malB gene (Table 5). For PCR, the genomic DNA was extracted from pure cultures of E. coli by the boiling method as previously described [61,62]. In brief, a pure colony from freshly grown culture was added into 100 µL phosphate buffer solution (PBS) in a sterile Eppendorf tube and mixed by gentle vortexing.…”
Section: Molecular Detection Of E Colimentioning
confidence: 99%