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Phylogenetic and molecular analyses of human parainfluenza type 3 virus in Buenos Aires, Argentina, between 2009 and 2013: The emergence of new genetic lineages.
Goya, Stephanie; Mistchenko, Alicia Susana; Viegas, Mariana.
Affiliation
  • Goya S; Virology Laboratory, Ricardo Gutierrez Children's Hospital, Buenos Aires City, Argentina, Gallo 1330 2°, (1425) Ciudad Autónoma Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina. Electronic address: goyastephanie@gmail.com.
  • Mistchenko AS; Virology Laboratory, Ricardo Gutierrez Children's Hospital, Buenos Aires City, Argentina, Gallo 1330 2°, (1425) Ciudad Autónoma Buenos Aires, Argentina; Comisión de Investigaciones Científicas de la Provincia de Buenos Aires (CIC), Buenos Aires, Argentina. Electronic address: asmistchenko@hotmail.com.
  • Viegas M; Virology Laboratory, Ricardo Gutierrez Children's Hospital, Buenos Aires City, Argentina, Gallo 1330 2°, (1425) Ciudad Autónoma Buenos Aires, Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentina. Electronic address: viegasmariana@conicet.gov.ar.
Infect Genet Evol ; 39: 85-91, 2016 Apr.
Article in En | MEDLINE | ID: mdl-26780643
Despite that human parainfluenza type 3 viruses (HPIV3) are one of the leading causes of acute lower respiratory tract infections in children under five, there is no licensed vaccine and there is limited current information on the molecular characteristics of regional and global circulating strains. The aim of this study was to describe the molecular characterization of HPIV3 circulating in Buenos Aires. We performed a genetic and phylogenetic analysis of the HN glycoprotein gene. Between 2009 and 2013, 124 HPIV3-positive samples taken from hospitalized pediatric patients were analyzed. Four new genetic lineages were described. Among them, C1c and C3d lineages showed local circulation patterns, whereas C3e and C3f comprised sequences from very distant countries. Despite the diversity of the described genotypes, C3a and C3d predominated over the others, the latter was present during the first years of the study and it was progressively replaced by C3a. Molecular analyses showed 28 non-synonymous substitutions; of these, 13 were located in potentially predicted B-cell epitopes. Taken together, the emergence of genetic lineages and the information of the molecular characteristics of HN protein may contribute to the general knowledge of HPIV3 molecular epidemiology for future vaccine development and antiviral therapies.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respirovirus Infections / Genetic Variation / HN Protein / Parainfluenza Virus 3, Human Type of study: Prognostic_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: America do sul / Argentina Language: En Journal: Infect Genet Evol Journal subject: BIOLOGIA / DOENCAS TRANSMISSIVEIS / GENETICA Year: 2016 Document type: Article Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respirovirus Infections / Genetic Variation / HN Protein / Parainfluenza Virus 3, Human Type of study: Prognostic_studies Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: America do sul / Argentina Language: En Journal: Infect Genet Evol Journal subject: BIOLOGIA / DOENCAS TRANSMISSIVEIS / GENETICA Year: 2016 Document type: Article Country of publication: Netherlands