4.5 Article

Occurrence and characterization of seven major Shiga toxin-producing Escherichia coli serotypes from healthy cattle on cow-calf operations in South Africa

期刊

ZOONOSES AND PUBLIC HEALTH
卷 65, 期 7, 页码 777-789

出版社

WILEY
DOI: 10.1111/zph.12491

关键词

cattle; cow-calf operations; major seven STEC; non-O157; serotypes; virulence

资金

  1. National Research Foundation (NRF) - Thuthuka Fund
  2. Global Disease Detection (GDD) Program of the Centers for Disease Control and Prevention (CDC) [1U2GGH001874-01]
  3. University of Pretoria, Institutional Research Theme (IRT)-Animal and Zoonotic Diseases (AZD) [UP-AZD IRT A0W596]
  4. Gauteng Department of Agriculture Rural Development (GDARD) [FY 2013/14-A0W907]

向作者/读者索取更多资源

Cattle are a major reservoir of Shiga toxin-producing Escherichia coli. This study investigated the occurrence of seven major STEC serogroups including O157, O145, O103, O121, O111, O45 and O26 among 578 STEC isolates previously recovered from 559 cattle. The isolates were characterized for serotype and major virulence genes. Polymerase chain reaction revealed that 41.7% (241/578) of isolates belonged to STEC O157, O145, O103, O121, O45 and O26, and 33 distinct serotypes. The 241 isolates corresponded to 16.5% (92/559) of cattle that were STEC positive. The prevalence of cattle that tested positive for at least one of the six serogroups across the five farms was variable ranging from 2.9% to 43.4%. Occurrence rates for individual serogroups were as follows: STEC O26 was found in 10.2% (57/559); O45 in 2.9% (16/559); O145 in 2.5% (14/559); O157 in 1.4% (8/559); O121 in 1.1% (6/559); and O103 in 0.4% (2/559). The following proportions of virulence genes were observed: stx1, 69.3% (167/241); stx2, 96.3% (232/241); eaeA, 7.1% (17/241); ehxA, 92.5% (223/241); and both stx1 and stx2, 62.2% (150/241) of isolates. These findings are evidence that cattle in South Africa carry STEC that belong to six major STEC serogroups commonly incriminated in human disease. However, only a subset of serotypes associated with these serogroups were clinically relevant in human disease. Most STEC isolates carried stx1, stx2 and ehxA but lacked eaeA, a major STEC virulence factor in human disease.

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