Molecular profiling and antimicrobial resistance of Shiga toxin-producing Escherichia coli O26, O45, O103, O121, O145 and O157 isolates from cattle on cow-calf operations in South Africa

In this study, 140 cattle STEC isolates belonging to serogroups O157, O26, O145, O121, O103 and O45 were characterized for 38 virulence-associated genes, antimicrobial resistance profiles and genotyped by PFGE. The majority of isolates carried both stx1 and stx 2 concurrently, stx2c , and stx2d ; pl...

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Veröffentlicht in:Scientific reports 2019-08, Vol.9 (1), p.11930-15, Article 11930
Hauptverfasser: Karama, Musafiri, Mainga, Alfred O., Cenci-Goga, Beniamino T., Malahlela, Mogaugedi, El-Ashram, Saeed, Kalake, Alan
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Sprache:eng
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Zusammenfassung:In this study, 140 cattle STEC isolates belonging to serogroups O157, O26, O145, O121, O103 and O45 were characterized for 38 virulence-associated genes, antimicrobial resistance profiles and genotyped by PFGE. The majority of isolates carried both stx1 and stx 2 concurrently, stx2c , and stx2d ; plasmid-encoded genes ehxA, espP, subA and saa but lacked katP and etpD and eaeA . Possession of eaeA was significantly associated with the presence of nle genes, katP , etpD , ureC and terC . However, saa and subA, stx1c and stx1d were only detected in eaeA negative isolates. A complete OI-122 and most non-LEE effector genes were detected in only two eaeA positive serotypes, including STEC O157:H7 and O103:H2. The eaeA gene was detected in STEC serotypes that are commonly implicated in severe humans disease and outbreaks including STEC O157:H7, STEC O145:H28 and O103:H2. PFGE revealed that the isolates were highly diverse with very low rates of antimicrobial resistance. In conclusion, only a small number of cattle STEC serotypes that possessed eaeA , had the highest number of virulence-associated genes, indicative of their high virulence. Further characterization of STEC O157:H7, STEC O145:H28 and O103:H2 using whole genome sequencing will be needed to fully understand their virulence potential for humans.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-019-47948-1