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Escherichia cryptic clade I is an emerging source of human intestinal pathogens.

Authors :
Okuno, Miki
Arimizu, Yoko
Miyahara, Seina
Wakabayashi, Yuki
Gotoh, Yasuhiro
Yoshino, Shuji
Harada, Tetsuya
Seto, Kazuko
Yamamoto, Takeshi
Nakamura, Keiji
Hayashi, Tetsuya
Ogura, Yoshitoshi
Source :
BMC Biology. 4/13/2023, Vol. 21 Issue 1, p1-16. 16p.
Publication Year :
2023

Abstract

Background: Within the genus Escherichia, several monophyletic clades other than the traditionally defined species have been identified. Of these, cryptic clade I (C-I) appears to represent a subspecies of E. coli, but due to the difficulty in distinguishing it from E. coli sensu stricto, the population structure and virulence potential of C-I are unclear. Results: We defined a set of true C-I strains (n = 465), including a Shiga toxin 2a (Stx2a)-producing isolate from a patient with bloody diarrhoea identified by the retrospective analyses using a C-I-specific detection system. Through genomic analysis of 804 isolates from the cryptic clades, including these C-I strains, we revealed their global population structures and the marked accumulation of virulence genes and antimicrobial resistance genes in C-I. In particular, half of the C-I strains contained hallmark virulence genes of Stx-producing E. coli (STEC) and/or enterotoxigenic E. coli (ETEC). We also found the host-specific distributions of virulence genes, which suggests bovines as the potential source of human infections caused by STEC- and STEC/ETEC hybrid-type C-I strains, as is known in STEC. Conclusions: Our findings demonstrate the emergence of human intestinal pathogens in C-I lineage. To better understand the features of C-I strains and their infections, extensive surveillance and larger population studies of C-I strains are needed. The C-I-specific detection system developed in this study will be a powerful tool for screening and identifying C-I strains. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17417007
Volume :
21
Issue :
1
Database :
Academic Search Index
Journal :
BMC Biology
Publication Type :
Academic Journal
Accession number :
163098277
Full Text :
https://doi.org/10.1186/s12915-023-01584-4