State Key Laboratory of Emerging Infectious Diseases, Department of Microbiology, The University of Hong Kong, Queen Mary Hospital, Pok Fu Lam, Hong Kong Island, Hong Kong.
PLoS One. 2012;7(8):e43986. doi: 10.1371/journal.pone.0043986. Epub 2012 Aug 24.
The discovery of novel viruses in animals expands our knowledge of viral diversity and potentially emerging zoonoses. High-throughput sequencing (HTS) technology gives millions or even billions of sequence reads per run, allowing a comprehensive survey of the genetic content within a sample without prior nucleic acid amplification. In this study, we screened 156 rectal swab samples from apparently healthy bats (n = 96), pigs (n = 9), cattles (n = 9), stray dogs (n = 11), stray cats (n = 11) and monkeys (n = 20) using a HTS metagenomics approach. The complete genome of a novel papillomavirus (PV), Miniopterus schreibersii papillomavirus type 1 (MscPV1), with L1 of 60% nucleotide identity to Canine papillomavirus (CPV6), was identified in a specimen from a Common Bent-wing Bat (M. schreibersii). It is about 7.5kb in length, with a G+C content of 45.8% and a genomic organization similar to that of other PVs. Despite the higher nucleotide identity between the genomes of MscPV1 and CPV6, maximum-likelihood phylogenetic analysis of the L1 gene sequence showed that MscPV1 and Erethizon dorsatum papillomavirus (EdPV1) are most closely related. Estimated divergence time of MscPV1 from the EdPV1/MscPV1 common ancestor was approximately 60.2-91.9 millions of years ago, inferred under strict clocks using the L1 and E1 genes. The estimates were limited by the lack of reliable calibration points from co-divergence because of possible host shifts. As the nucleotide sequence of this virus only showed limited similarity with that of related animal PVs, the conventional approach of PCR using consensus primers would be unlikely to have detected the novel virus in the sample. Unlike the first bat papillomavirus RaPV1, MscPV1 was found in an asymptomatic bat with no apparent mucosal or skin lesions whereas RaPV1 was detected in the basosquamous carcinoma of a fruit bat Rousettus aegyptiacus. We propose MscPV1 as the first member of the novel Dyolambda-papillomavirus genus.
本研究采用高通量测序(HTS)技术,对 156 份来自健康蝙蝠(n=96)、猪(n=9)、牛(n=9)、流浪狗(n=11)、流浪猫(n=11)和猴子(n=20)的直肠拭子样本进行检测,发现了一种新型乳头瘤病毒(PV)——Miniopterus schreibersii 乳头瘤病毒 1 型(MscPV1)。该病毒的全长基因组与犬乳头瘤病毒(CPV6)的 L1 核苷酸序列具有 60%的同源性,存在于一只普通长翼蝠(M. schreibersii)的样本中。该病毒基因组全长约 7.5kb,G+C 含量为 45.8%,基因组组织与其他 PV 相似。尽管 MscPV1 和 CPV6 基因组之间的核苷酸同一性较高,但 L1 基因序列的最大似然系统发育分析表明,MscPV1 与 Erethizon dorsatum 乳头瘤病毒(EdPV1)亲缘关系最近。使用 L1 和 E1 基因,在严格的时钟下对 MscPV1 与 EdPV1/MscPV1 共同祖先的分歧时间进行估算,结果约为 60.2-91.9 百万年前。由于可能发生宿主转移,缺乏共同进化的可靠校准点,因此这些估计值受到限制。由于与相关动物乳头瘤病毒的核苷酸序列相似性有限,因此使用共识引物进行 PCR 的传统方法不太可能在样本中检测到这种新型病毒。与第一种蝙蝠乳头瘤病毒 RaPV1 不同,MscPV1 存在于无症状的蝙蝠中,没有明显的粘膜或皮肤损伤,而 RaPV1 则存在于果蝠 Rousettus aegyptiacus 的基底鳞状细胞癌中。我们提出 MscPV1 是新型 Dyolambda-papillomavirus 属的第一个成员。