期刊论文详细信息
BMC Research Notes
Molecular characteristics of rotavirus genotypes circulating in the south of Benin, 2016–2018
Osseni Razack1  Annick Capo-Chichi2  Honore Sourou Bankole3  Jijoho Michel Agbla3  Tamegnon Victorien Dougnon4  Alidehou Jerrold Agbankpe4  Rashi Gautam5  Mathew D. Esona5  Michael D. Bowen5 
[1] Central Clinic of Abomey Calavi, 01 P.O. Box 418, Cotonou, Benin;Epidemiological Surveillance Service, Ministry of Public Health, 01 P.O. Box 418, Cotonou, Benin;Ministry of Public Health, National Health Laboratory, 01 P.O. Box 418, Cotonou, Benin;Research Unit in Applied Microbiology and Pharmacology of Natural Substances, Research Laboratory in Applied Biology, Polytechnic School of Abomey-Calavi, University of Abomey-Calavi, 01 P.O. Box 2009, Cotonou, Benin;Research Unit in Applied Microbiology and Pharmacology of Natural Substances, Research Laboratory in Applied Biology, Polytechnic School of Abomey-Calavi, University of Abomey-Calavi, 01 P.O. Box 2009, Cotonou, Benin;Viral Gastroenteritis Branch, Division of Viral Diseases, NCIRD, Centers for Disease Control CDC, 1600 Clifton Road, NE, 30329, Atlanta, GA, USA;
关键词: Pediatric;    Rotavirus;    Surveillance;    Genotypes;    Benin;   
DOI  :  10.1186/s13104-020-05332-7
来源: Springer
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【 摘 要 】

ObjectiveRotavirus remains the main causative agent of gastroenteritis in young children in countries that have not yet introduced the vaccine. In Benin, rotavirus vaccine was introduced late December 2019 into the EPI. This study aims to provide pre-vaccination era rotavirus genotyping data in Benin. These data can supplement data from the surveillance system of Ministry of Health of Benin which is supported by the World Health Organization (WHO).ResultsOf the 420 diarrheal stool samples, actively collected in southern Benin from July 2016 through November 2018 from children under 5 years old and suffering from gastroenteritis, 167 (39.8%) samples were rotavirus EIA positive. 186 (44.3%) samples contained amplifiable rotavirus RNA detected by qRT-PCR method and were genotyped using one-step RT-PCR multiplex genotyping method. G1P[8] represents the predominant genotype (32%) followed by the G2P[4] (26%), G3P[6] (16%), G12P[8] (13%) and mixed G and P types (1%). Four samples (2%) could not be assigned both G and P type specificity.

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