Diversity of rotavirus strains circulating in Haiti before and after introduction of monovalent vaccine.

Haiti Pre- and post-vaccination RT-PCR Rotavirus genotypes

Journal

IJID regions
ISSN: 2772-7076
Titre abrégé: IJID Reg
Pays: England
ID NLM: 9918418183106676

Informations de publication

Date de publication:
Sep 2022
Historique:
received: 16 05 2022
revised: 05 07 2022
accepted: 06 07 2022
entrez: 4 8 2022
pubmed: 5 8 2022
medline: 5 8 2022
Statut: epublish

Résumé

Haiti introduced a monovalent human group A rotavirus (RVA) vaccine (Rotarix) into its routine infant immunization program in April 2014. The goal of the surveillance program was to characterize RVA strains circulating in Haiti before and after RVA vaccine introduction. Stool samples were collected from children <5 years old presenting with acute gastroenteritis at 16 hospitals in Haiti. RVA antigen enzyme immunoassay (EIA) testing was performed, and G and P genotypes were determined for positive specimens. In this study, genotype data for samples collected from May 2012 through April 2014 (the pre-vaccine introduction era) and May 2014 through July 2019 (post-vaccine introduction era) were analyzed. A total of 809 specimens were tested by the Centers for Disease Control and Prevention. During the pre-vaccine introduction era (May 2012 through April 2014), G12P[8] was the predominant genotype, detected in 88-94% of specimens. There was a high prevalence of the equine-like G3P[8] genotype among Haitian children with RVA after vaccine introduction. The predominance of equine-like G3P[8] in three of five RVA seasons post-vaccine introduction suggests possible vaccine-specific selection pressure in Haiti. These temporal variations in RVA genotype predominance will require continued monitoring in Haiti as the vaccination program continues.

Sections du résumé

Background UNASSIGNED
Haiti introduced a monovalent human group A rotavirus (RVA) vaccine (Rotarix) into its routine infant immunization program in April 2014. The goal of the surveillance program was to characterize RVA strains circulating in Haiti before and after RVA vaccine introduction.
Methods UNASSIGNED
Stool samples were collected from children <5 years old presenting with acute gastroenteritis at 16 hospitals in Haiti. RVA antigen enzyme immunoassay (EIA) testing was performed, and G and P genotypes were determined for positive specimens. In this study, genotype data for samples collected from May 2012 through April 2014 (the pre-vaccine introduction era) and May 2014 through July 2019 (post-vaccine introduction era) were analyzed.
Results UNASSIGNED
A total of 809 specimens were tested by the Centers for Disease Control and Prevention. During the pre-vaccine introduction era (May 2012 through April 2014), G12P[8] was the predominant genotype, detected in 88-94% of specimens. There was a high prevalence of the equine-like G3P[8] genotype among Haitian children with RVA after vaccine introduction.
Conclusions UNASSIGNED
The predominance of equine-like G3P[8] in three of five RVA seasons post-vaccine introduction suggests possible vaccine-specific selection pressure in Haiti. These temporal variations in RVA genotype predominance will require continued monitoring in Haiti as the vaccination program continues.

Identifiants

pubmed: 35923644
doi: 10.1016/j.ijregi.2022.07.007
pii: S2772-7076(22)00092-3
pmc: PMC9340491
doi:

Types de publication

Journal Article

Langues

eng

Pagination

146-151

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

© 2022 Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.

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Auteurs

Mentor Ali Ber Lucien (MAB)

Laboratoire National de Santé Publique, Port-au-Prince, Haiti.

Mathew D Esona (MD)

Division of Viral Diseases, National Center for Immunization and Respiratory Diseases (NCIRD), CDC, Atlanta, Georgia, USA.

Manise Pierre (M)

Pan American Health Organization (PAHO)/Haiti.

Gerard Joseph (G)

Laboratoire National de Santé Publique, Port-au-Prince, Haiti.

Chedelène Rivière (C)

Laboratoire National de Santé Publique, Port-au-Prince, Haiti.

Eyal Leshem (E)

Division of Viral Diseases, National Center for Immunization and Respiratory Diseases (NCIRD), CDC, Atlanta, Georgia, USA.

Negar Aliabadi (N)

Division of Viral Diseases, National Center for Immunization and Respiratory Diseases (NCIRD), CDC, Atlanta, Georgia, USA.

Anne Marie Desormeaux (AM)

CDC Country Office, Port-au-Prince, Haiti.

Jocelyn Andre-Alboth (J)

Laboratoire National de Santé Publique, Port-au-Prince, Haiti.

David L Fitter (DL)

CDC Country Office, Port-au-Prince, Haiti.

Yoran Grant-Greene (Y)

CDC Country Office, Port-au-Prince, Haiti.

Jacqueline Tate (J)

Division of Viral Diseases, National Center for Immunization and Respiratory Diseases (NCIRD), CDC, Atlanta, Georgia, USA.

Jacques Boncy (J)

Laboratoire National de Santé Publique, Port-au-Prince, Haiti.

Roopal Patel (R)

CDC Country Office, Port-au-Prince, Haiti.

Eleanor Burnett (E)

Division of Viral Diseases, National Center for Immunization and Respiratory Diseases (NCIRD), CDC, Atlanta, Georgia, USA.

Stanley Juin (S)

CDC Country Office, Port-au-Prince, Haiti.

Umesh D Parashar (UD)

Division of Viral Diseases, National Center for Immunization and Respiratory Diseases (NCIRD), CDC, Atlanta, Georgia, USA.

Michael D Bowen (MD)

Division of Viral Diseases, National Center for Immunization and Respiratory Diseases (NCIRD), CDC, Atlanta, Georgia, USA.

Classifications MeSH