Global Genomic Epidemiology of Escherichia coli (ExPEC) ST38 Lineage Revealed a Virulome Associated with Human Infections.

Autor:	Fonseca EL; Laboratório de Genética Molecular de Microrganismos, Instituto Oswaldo Cruz-FIOCRUZ, Rio de Janeiro 21040-360, RJ, Brazil., Morgado SM; Laboratório de Genética Molecular de Microrganismos, Instituto Oswaldo Cruz-FIOCRUZ, Rio de Janeiro 21040-360, RJ, Brazil., Caldart RV; Centro de Ciências da Saúde, Universidade Federal de Roraima, Boa Vista 69300-000, RR, Brazil., Vicente AC; Laboratório de Genética Molecular de Microrganismos, Instituto Oswaldo Cruz-FIOCRUZ, Rio de Janeiro 21040-360, RJ, Brazil.
Jazyk:	angličtina
Zdroj:	Microorganisms [Microorganisms] 2022 Dec 15; Vol. 10 (12). Date of Electronic Publication: 2022 Dec 15.
DOI:	10.3390/microorganisms10122482
Abstrakt:	Background: Most of the extraintestinal human infections worldwide are caused by specific extraintestinal pathogenic Escherichia coli (ExPEC) lineages, which also present a zoonotic character. One of these lineages belongs to ST38, a high-risk globally disseminated ExPEC. To get insights on the aspects of the global ST38 epidemiology and evolution as a multidrug-resistant and pathogenic lineage concerning the three axes of the One Health concept (humans, animals, and natural environments), this study performed a global phylogenomic analysis on ST38 genomes. Methods: A phylogenetic reconstruction based on 376 ST38 genomes recovered from environments, humans, livestock, and wild and domestic animals in all continents throughout three decades was performed. The global information concerning the ST38 resistome and virulome was also approached by in silico analyses. Results: In general, the phylogenomic analyses corroborated the zoonotic character of the ExPEC ST38, since clonal strains were recovered from both animal and human sources distributed worldwide. Moreover, our findings revealed that, independent of host sources and geographic origin, the genomes were distributed in two major clades (Clades 1 and 2). However, the ST38 accessory genome was not strictly associated with clades and sub-clades, as found for the type 2 T3SS ETT2 that was evenly distributed throughout Clades 1 and 2. Of note was the presence of the Yersinia pestis -like high-pathogenicity island (HPI) exclusively in the major Clade 2, in which prevails most of the genomes from human origin recovered worldwide (2000 to 2020). Conclusions: This evidence corroborates the HPI association with successful E. coli ST38 establishment in human infections.
Databáze:	MEDLINE
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