Cholera between 1991 and 1997 in Mexico Was Associated with Infection by Classical, El Tor, and El Tor Variants of
Vibrio cholerae
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Published:2010-10
Issue:10
Volume:48
Page:3666-3674
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ISSN:0095-1137
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Container-title:Journal of Clinical Microbiology
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language:en
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Short-container-title:J Clin Microbiol
Author:
Alam Munirul1, Nusrin Suraia1, Islam Atiqul1, Bhuiyan Nurul A.1, Rahim Niaz1, Delgado Gabriela2, Morales Rosario2, Mendez Jose Luis2, Navarro Armando2, Gil Ana I.3, Watanabe Haruo4, Morita Masatomo4, Nair G. Balakrish5, Cravioto Alejandro1
Affiliation:
1. International Center for Diarrhoeal Disease Research, Bangladesh (ICDDR,B), Mohakhali, Dhaka 1212, Bangladesh 2. Department of Public Health, Faculty of Medicine, Universidad Nacional Autónoma de México, Mexico, D.F., Mexico 3. Instituto de Investigación Nutricional, Lima, Peru 4. National Institute of Infectious Diseases, Shinjuku-ku, Tokyo, Japan 5. National Institute of Cholera and Enteric Diseases, Kolkata, India
Abstract
ABSTRACT
Vibrio cholerae
O1 biotype El Tor (ET), the cause of the current 7th pandemic, has recently been replaced in Asia and Africa by an altered ET biotype possessing cholera toxin (CTX) of the classical (CL) biotype that originally caused the first six pandemics before becoming extinct in the 1980s. Until recently, the ET prototype was the biotype circulating in Peru; a detailed understanding of the evolutionary trend of
V. cholerae
causing endemic cholera in Latin America is lacking. The present retrospective microbiological, molecular, and phylogenetic study of
V. cholerae
isolates recovered in Mexico (
n
= 91; 1983 to 1997) shows the existence of the pre-1991 CL biotype and the ET and CL biotypes together with the altered ET biotype in both epidemic and endemic cholera between 1991 and 1997. According to sero- and biotyping data, the altered ET, which has shown predominance in Mexico since 1991, emerged locally from ET and CL progenitors that were found coexisting until 1997. In Latin America, ET and CL variants shared a variable number of phenotypic markers, while the altered ET strains had genes encoding the CL CTX (CTX
CL
) prophage,
ctxB
CL
and
rstR
CL
, in addition to resident
rstR
ET
, as the underlying regional signature. The distinct regional fingerprints for ET in Mexico and Peru and their divergence from ET in Asia and Africa, as confirmed by subclustering patterns in a pulsed-field gel electrophoresis (NotI)-based dendrogram, suggest that the Mexico epidemic in 1991 may have been a local event and not an extension of the epidemics occurring in Asia and South America. Finally, the CL biotype reservoir in Mexico is unprecedented and must have contributed to the changing epidemiology of global cholera in ways that need to be understood.
Publisher
American Society for Microbiology
Subject
Microbiology (medical)
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