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Detailed genetic analysis of hemagglutinin-neuraminidase glycoprotein gene in human parainfluenza virus type 1 isolates from patients with acute respiratory infection between 2002 and 2009 in Yamagata prefecture, Japan

DOI: 10.1186/1743-422x-8-533

Keywords: Human parainfluenza virus, Maximum likelihood (ML) method, Phylogenetic analysis

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Abstract:

A few substitutions of nucleotides in the second binding site of HN gene were observed among the present isolates. The strains were classified into two major clusters in the phylogenetic tree by the NJ method. Another phylogenetic tree constructed by the ML method showed that the strains diversified in the late 1980s. No positively selected sites were found in the present strains. Moreover, the pairwise distance among the present isolates was relatively short.The evolution of HN gene in the present HPIV1 isolates was relatively slow. The ML method may be a useful phylogenetic method to estimate the evolutionary time scale of HPIV and other viruses.Human parainfluenza virus type 1 (HPIV1) of the genus Respirovirus and family Paramyxoviridae causes various acute respiratory infections (ARI) including the common cold, croup, bronchiolitis, and pneumonia [1]. Epidemiological data suggest that HPIV types 1-4 mainly infect younger children at least once, although reinfections may occur in adults [2,3]. Indeed, serological surveys indicate that at least 75% of children have been infected with HPIV1 by 5 years of age [4,5]. HPIV1 and 3 show high prevalence and are associated with up to 12% of acute lower respiratory tract infections in adults [6]. Thus, HPIVs, including HPIV1, may be major agents of ARI throughout the world [7-9].HPIV possess two major surface glycoproteins: hemagglutinin-neuraminidase (HN) glycoprotein and fusion protein (F protein) [1]. HN glycoprotein shows multiple biological functions that include hemagglutinin and enzymatic activities as neuraminidase [3,10]. As a result, this molecule regulates viral adsorption and entry, and regulates the release of progeny virions from the infected cell surface [3]. In addition, it is suggested that HN glycoprotein is a major antigen [1]. The detailed molecular characteristics of HN glycoprotein have been confirmed in HPIV3, while those in HPIV1 remain unclear [11]. In addition, the genetic characteristics of HPIV1

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