In the present study, different fly species were associated with foodborne and other pathogens. Wild synanthropic flies belonging to 12 species of 12 genera were caught for the isolation and identification of microorganisms, which might have been possibly transmitted by these flies. Trapping of flies was done at different domestic animal related places (dog pound, poultry house, cattle barn, horse stable, pigpen). All 56 individual flies were shown to be carriers of multiple species of microorganisms. Furthermore, the capacity for the flies to act as vectors was demonstrated by successful transfer of the microorganisms from live flies to blood agar plates. Potentially pathogenic and several non-pathogenic microorganisms were found. Among them, a series of pathogenic Escherichia coli strains (EAEC, EPEC, ETEC) was identified. This is the first study to clearly demonstrate the potential of these flies as vectors for the transmission of pathogenic microorganisms.
In the current study, samples of 50 synanthropic flies were collected from each of five rural locations used for domestic animal husbandry (specifically a cattle barn, a dog pound, a horse stable, and a pigpen). Flies were examined using a variety of microbiological methods to determine the pathogenic agents that they carried. The most frequently sampled species were Musca domestica (L.) (51%) followed by Stomoxys calcitrans (L.) (24%). All fly species were found to carry an array of different pathogenic bacterial and fungal species. Among these were human pathogens such as Campylobacter jejuni and Escherichia coli-strains (EHEC, EPEC, and ETEC) and the fungi Candida albicans and Candida tropicalis. The germs could be detected in the intestines as well as on the exoskeletons of the flies. The current study confirms and supplements the general knowledge about pathogens that may be transmitted to domestic animals and humans by synanthropic flies.
BackgroundCause for gastroenteritis range from viral, bacterial to parasitic pathogens. Rapid Multiplexing techniques like ProGastro_SSCS and xTAG_GPP can detect broad panels of pathogens simultaneously.We performed a field test with a total number of 347 stool samples from adult hospitalized patients that were tested with the Luminex xTAG GPP assay; of the 157 samples positively tested for at least one pathogen by xTAG GPP a total number of 30 samples was retested with the ProGastro SSCS assay. Assays were compared to standard routine diagnostics.FindingsMultiplexing significantly reduced the time to the initial identification of a pathogen. Moreover, multiplexing detected pathogens for which a diagnostic assays was not requested by the physician and thus may be an important tool for avoiding nosocomial outbreaks.ConclusionThis first frontline approach with these assays approves their utility compared to conventional microbiological methods.
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