Ganesh Balasubramanian, Nagashima Shigeo, Ghosh Souvik, Nataraju Seegekote M, Rajendran Krishnan, Manna Byomkesh, Ramamurthy Thandavarayan, Niyogi Swapan K, Kanungo Suman, Sur Dipika, Kobayashi Nobumichi, Krishnan Triveni
Int J Mol Epidemiol Genet. 2011 Jan 1;2(1):61-72. Epub 2010 Dec 27.
Picobirnaviruses (PBVs) associated with viral gastroenteritis were reported from humans and several animal species to date. PBVs belonging to family Picobirnaviridae under proposed order Diplornavirales are small, non-enveloped, with bisegmented dsRNA genome.
PBV was detected by polyacrylamide gel electrophoresis (PAGE) and silver staining. Confirmatory RT-PCR using primer pair PicoB25 (+) and PicoB43 (-) for genogroup I PBV and PicoB23(+) and PicoB24(-) for genogroup II PBV, resulted in amplicons of 201bp and 369bp respectively. The amplicons of genogroup I PBV were cloned and sequenced; amplicon of genogroup II PBV was directly sequenced. Further, the phylogenetic relationship and genetic diversity of strains from Kolkata was compared with hitherto reported PBV strains.
In PAGE, a faecal specimen showed three sets of PBV with large profile bisegmented genomic RNA with slight variation in migration pattern. Molecular cloning experiments confirmed that PBV/ Human/INDIA/GPBV6/2007 had mixed infection comprising four different strains of PBV genogroup I [GPBV6C1P-GPBV6C4P] and one PBV genogroup II strain [GPBV6G2P].
Sequence comparison and phylogenetic analysis of gene segment 2 of GPBV6 clones (C1, C2, C3 and C4) revealed low nucleotide identities (59-63%) and distant genetic relatedness to other human and porcine genogroup I picobirnaviruses. The strain GPBV6G2P represents another PBV genogroup II strain after prototype strain 4-GA-91/USA as genogroup II PBVs have seldom been reported to date, except from Kolkata, India and Netherlands. We are reporting the first incidence of detection of multiple strain (mixed) infection of picobirnavirus [genogroups I and II] from a diarrhoeic child in a slum community of Kolkata, India.
迄今为止,已在人类和多种动物物种中报道了与病毒性肠胃炎相关的微小双节段RNA病毒(PBV)。属于双分病毒目下拟病毒科的PBV体积小,无包膜,具有双节段双链RNA基因组。
通过聚丙烯酰胺凝胶电泳(PAGE)和银染检测PBV。使用针对I基因组PBV的引物对PicoB25(+)和PicoB43(-)以及针对II基因组PBV的引物对PicoB23(+)和PicoB24(-)进行验证性逆转录聚合酶链反应(RT-PCR),分别得到201bp和369bp的扩增子。对I基因组PBV的扩增子进行克隆和测序;对II基因组PBV的扩增子直接测序。此外,将来自加尔各答的毒株的系统发育关系和遗传多样性与迄今报道的PBV毒株进行比较。
在PAGE中,一份粪便标本显示出三组PBV,其双节段基因组RNA条带较大,迁移模式略有差异。分子克隆实验证实,PBV/人类/印度/GPBV6/2007存在混合感染,包括四种不同的I基因组PBV毒株[GPBV6C1P - GPBV6C4P]和一种II基因组PBV毒株[GPBV6G2P]。
对GPBV6克隆(C1、C2、C3和C4)的基因片段2进行序列比较和系统发育分析,发现其与其他人类和猪I基因组微小双节段RNA病毒的核苷酸同一性较低(59 - 63%),遗传关系较远。菌株GPBV6G2P代表继原型毒株4 - GA - 91/美国之后的另一种II基因组PBV毒株,因为迄今为止,除了来自印度加尔各答和荷兰的报道外,II基因组PBV很少被报道。我们报告了在印度加尔各答一个贫民窟社区的腹泻儿童中首次检测到微小双节段RNA病毒[I和II基因组]的多毒株(混合)感染情况。