Multiplex PCR Assays for the Detection of One Hundred and Thirty Seven Serogroups of Shiga Toxin-Producing Escherichia coli Associated With Cattle

• Published in: Frontiers in cellular and infection microbiology 2020-07, Vol.10, p.378-378
• Main Authors: Ludwig, Justin B, Shi, Xiaorong, Shridhar, Pragathi B, Roberts, Elisabeth L, DebRoy, Chitrita, Phebus, Randy K, Bai, Jianfa, Nagaraja, T G
• Format: Article
• Language: English
• Subjects: cattle; Cellular and Infection Microbiology; feces; Multiplex PCR assays; non-top-7 STEC; shiga toxin-producing Escherichia coli (STEC); top-7 STEC
• ISSN: 2235-2988; 2235-2988
• DOI: 10.3389/fcimb.2020.00378

carrying prophage with genes that encode for Shiga toxins are categorized as Shiga toxin-producing (STEC) pathotype. Illnesses caused by STEC in humans, which are often foodborne, range from mild to bloody diarrhea with life-threatening complications of renal failure and hemolytic uremic syndrome and even death, particularly in children. As many as 158 of the total 187 serogroups of are known to carry Shiga toxin genes, which makes STEC a major pathotype of . Seven STEC serogroups, called top-7, which include O26, O45, O103, O111, O121, O145, and O157, are responsible for the majority of the STEC-associated human illnesses. The STEC serogroups, other than the top-7, called "non-top-7" have also been associated with human illnesses, more often as sporadic infections. Ruminants, particularly cattle, are principal reservoirs of STEC and harbor the organisms in the hindgut and shed in the feces, which serves as a major source of food and water contaminations. A number of studies have reported on the fecal prevalence of top-7 STEC in cattle feces. However, there is paucity of data on the prevalence of non-top-7 STEC serogroups in cattle feces, generally because of lack of validated detection methods. The objective of our study was to develop and validate 14 sets of multiplex PCR (mPCR) assays targeting serogroup-specific genes to detect 137 non-top-7 STEC serogroups previously reported to be present in cattle feces. Each assay included 7-12 serogroups and primers were designed to amplify the target genes with distinct amplicon sizes for each serogroup that can be readily identified within each assay. The assays were validated with 460 strains of known serogroups. The multiplex PCR assays designed in our study can be readily adapted by most laboratories for rapid identification of strains belonging to the non-top-7 STEC serogroups associated with cattle.