Genetic variability among group A and B respiratory syncytial viruses in Mozambique: identification of a new cluster of group B isolates

Epidemiología y Bioestadística 1 and Hepatología-IMD 2 , Fundació Clínic, IDIBAPS, Hospital Clínic, Universidad de Barcelona, Villaroel 170, 08036 Barcelona, Spain Centro de Investigaçao en Saude da Manhiça, INS-Ministerio da Saude, Mozambique 3 Servicio de Virología, Centro Nacional de Microbiologí...

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Published in:Journal of general virology Vol. 82; no. 1; pp. 103 - 111
Main Authors: Roca, Anna, Loscertales, Mari-Paz, Quinto, Llorenc, Perez-Brena, Pilar, Vaz, Neide, Alonso, Pedro-Luis, Saiz, Juan-Carlos
Format: Journal Article
Language:English
Published: England Soc General Microbiol 01-01-2001
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Summary:Epidemiología y Bioestadística 1 and Hepatología-IMD 2 , Fundació Clínic, IDIBAPS, Hospital Clínic, Universidad de Barcelona, Villaroel 170, 08036 Barcelona, Spain Centro de Investigaçao en Saude da Manhiça, INS-Ministerio da Saude, Mozambique 3 Servicio de Virología, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Madrid, Spain 4 Author for correspondence: Juan-Carlos Saiz. Fax +34 93 4515522. e-mail jcsaiz{at}medicina.ub.es Respiratory syncytial virus (RSV) is the major cause of acute lower respiratory tract infection in children and vulnerable adults, but little is known regarding RSV infection in Africa. In this report, a recent RSV outbreak in Mozambique was studied and results showed that 275 of 3192 (8·6%) nasopharyngeal aspirates tested were RSV-positive by ELISA. RSV presents two antigenic groups (A and B) with a high genetic and antigenic variability between and within them. Analysis by a new RFLP assay of RT–PCR amplified N protein gene products showed a higher prevalence of group B RSV than that of group A (85% versus 15%). However, genetic variability of the G protein gene was higher among group A RSV strains. The frequency and pattern of glycosylation sites were also quite different between both groups. In addition, two different phylogenetic clusters of Mozambican viruses were found within each group, but only sequences from cluster B-I were relatively distinct from previously described isolates. The implications of such differences in the antigenic and immunogenic characteristics of each group are discussed.
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ISSN:0022-1317
1465-2099
DOI:10.1099/0022-1317-82-1-103