Damanka Susan, Dennis Francis E, Agbemabiese Chantal, Lartey Belinda, Adiku Theophilus, Nyarko Kofi, Enweronu-Laryea Christabel C, Sagoe Kwamena W, Ofori Michael, Rodrigues Onike, Armah George E
Department of Electron Microscopy and Histopathology, Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Legon, Accra, Ghana.
Department of Microbiology, University of Ghana Medical School, College of Health Sciences, Accra, Ghana.
Virol J. 2016 Apr 22;13:69. doi: 10.1186/s12985-016-0523-5.
Rotaviruses with the P[8] genotype have been associated with majority of infections. Recent improvements in molecular diagnostics have delineated the P[8] genotype into P[8]a and P[8]b subtypes. P[8]a is the previously known P[8] genotype which is common whilst P[8]b subtype also known as OP354-like strain is genetically distinct, rarely detected and reported from a few countries. In a previous study, the P-types could not be determined for 80 RVA-positive samples by conventional RT-PCR genotyping methods with the recommended pool of P-genotype specific primers used in the WHO Regional Rotavirus Reference Laboratory in Ghana. The present study employed sequence-dependent cDNA amplification method to genotype previously non-typeable P-types.
Viral RNAs were extracted and rotavirus VP4 genes amplified by one step RT-PCR using gene specific primers. PCR amplicons were purified, sequenced and sequences aligned with cognate gene sequences available in GenBank using the ClustalW algorithm. Phylogenetic analysis was performed using the Neighbour-Joining method in MEGA v6.06 software. Phylogenetic tree was statistically supported by bootstrapping with 1000 replicates, and distances calculated using the Kimura-2 parameter model.
Of the 80 RVA-positive samples, 57 were successfully sequenced and characterized. Forty-eight of these were identified as P[8] strains of which 5 were characterized as the rare P[8]b subtype. Phylogenetic analysis of the VP8* fragment of the VP4 genes of these P[8]b strains revealed a close relationship with prototype OP354-like P[8]b strain and P[8]b strains of Russian and South African P[8]b origin.
The study highlights the importance of regularly updating the primers employed for molecular typing of rotaviruses.
P[8]基因型轮状病毒与大多数感染相关。分子诊断技术的最新进展已将P[8]基因型分为P[8]a和P[8]b亚型。P[8]a是先前已知的常见P[8]基因型,而P[8]b亚型也称为OP354样毒株,在基因上是不同的,很少被检测到,仅在少数国家有报道。在之前的一项研究中,使用加纳世卫组织区域轮状病毒参考实验室推荐的P基因型特异性引物库,通过传统RT-PCR基因分型方法无法确定80份轮状病毒A组(RVA)阳性样本的P型。本研究采用序列依赖性cDNA扩增方法对先前无法分型的P型进行基因分型。
提取病毒RNA,使用基因特异性引物通过一步RT-PCR扩增轮状病毒VP4基因。PCR扩增产物经纯化、测序,并使用ClustalW算法将序列与GenBank中可用的同源基因序列进行比对。使用MEGA v6.06软件中的邻接法进行系统发育分析。通过1000次重复的自展法对系统发育树进行统计学支持,并使用Kimura-2参数模型计算距离。
在80份RVA阳性样本中,57份成功测序并进行了特征分析。其中48份被鉴定为P[8]毒株,其中5份被鉴定为罕见的P[8]b亚型。对这些P[8]b毒株的VP4基因VP8*片段进行系统发育分析,发现与原型OP354样P[8]b毒株以及俄罗斯和南非P[8]b起源的P[8]b毒株关系密切。
该研究强调了定期更新用于轮状病毒分子分型的引物的重要性。