Combined usage of serodiagnosis and O antigen typing to isolate Shiga toxin-producing Escherichia coli O76:H7 from a hemolytic uremic syndrome case and genomic insights from the isolate

Author:

Lee Kenichi1ORCID,Iguchi Atsushi2ORCID,Terano Chikako34,Hataya Hiroshi3,Isobe Junko5,Seto Kazuko1,Ishijima Nozomi1,Akeda Yukihiro1,Ohnishi Makoto1,Iyoda Sunao1,Morimoto Yo,Ogawa Keiko,Ishiguro Makoto,Kikuchi Masayuki,Sampei Mika,Aoki Yoko,Seto Junji,Ishikawa Kanako,Sato Takashi,Kikuchi Koji,Tomari Kentaro,Ueno Hiroyuki,Hazama Kyoko,Kikuchi Takashi,Yajima Masayuki,Kanazawa Satoko,Kawase Masao,Kimata Keiko,Yuruzume Saya,Shiroza Mika,Kitagawa Emiko,Yoshikawa Misa,Yokoyama Koji,Ono Satoko,Furukawa Yumi,Matsuyama Miki,Furuta Ayako,Noda Makiko,Kameyama Yoshihiko,Aota Tatsuaki,Katamune Chiharu,Shimoda Yuko,Abe Yuri,Tamura Sawako,Furukawa Yurika,Obara Atsumi,

Affiliation:

1. Department of Bacteriology I, National Institute of Infectious Diseases , Tokyo, Japan

2. Department of Animal and Grassland Sciences, Faculty of Agriculture, University of Miyazaki , Miyazaki, Japan

3. Department of Nephrology and Rheumatology, Tokyo Metropolitan Children’s Medical Center , Tokyo, Japan

4. Department of Nephrology, Aichi Children’s Health and Medical Center , Aichi, Japan

5. Department of Bacteriology, Toyama Institute of Health , Imizu, Toyama, Japan

Abstract

ABSTRACT Minor O-serogroups of Shiga toxin-producing Escherichia coli (STEC) can cause severe clinical complications in humans, including hemolytic uremic syndrome (HUS). However, detection and isolation of these minor serogroups of STEC are challenging due to the lack of specific isolation methods. Here, we present a case of HUS in which STEC was not isolated by routine diagnostic tests for the major serotypes. Therefore, we tried a new diagnostic and isolation method that combines PCR screening, immunomagnetic bead separation, and serum agglutination tests and successfully isolated STEC O76. Subsequent genomic analyses of the STEC O76 isolates revealed that several isolates of this serogroup carrying stx2 were related to severe infections. The complete genome of the HUS-derived isolates provided two important implications. First, using a complete genome as a reference in core genome single nucleotide polymorphism analysis leads to the highest resolution of the analysis. Second, the HUS-derived STEC O76:H7 possessed two copies of Stx2a prophages, and one of them showed a “prophage integrating into prophage” structure, as described in STEC O145:H28. These results demonstrate that our detection methods contribute to the diagnosis and isolation of minor serogroups of STECs and complete genomic analyses can illuminate the pathogenic potential of STECs. IMPORTANCE Hemolytic uremic syndrome (HUS) is a life-threatening disease caused by Shiga toxin-producing Escherichia coli (STEC) infection. The treatment approaches for STEC-mediated typical HUS and atypical HUS differ, underscoring the importance of rapid and accurate diagnosis. However, specific detection methods for STECs other than major serogroups, such as O157, O26, and O111, are limited. This study focuses on the utility of PCR-based O-serotyping, serum agglutination tests utilizing antibodies against the identified Og type, and isolation techniques employing antibody-conjugated immunomagnetic beads for STEC isolation. By employing these methods, we successfully isolated a STEC strain of a minor serotype, O76:H7, from a HUS patient.

Funder

Japan Agency for Medical Research and Development

MEXT | Japan Society for the Promotion of Science

Ministry of Health, Labour and Welfare

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Cell Biology,Microbiology (medical),Genetics,General Immunology and Microbiology,Ecology,Physiology

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