Yin Li, Yao Jin, Chang Kaifen, Gardner Brent P, Yu Fahong, Giuliano Anna R, Goodenow Maureen M
Department of Pathology, Immunology & Laboratory Medicine and UF Health Cancer Center, University of Florida, Gainesville, FL 32610, USA.
Interdisciplinary Center for Biotechnology Research, University of Florida, Gainesville, FL 32610, USA.
Viruses. 2016 Jan 25;8(2):28. doi: 10.3390/v8020028.
Multiple-type human papillomaviruses (HPV) infection presents a greater risk for persistence in asymptomatic individuals and may accelerate cancer development. To extend the scope of HPV types defined by probe-based assays, multiplexing deep sequencing of HPV L1, coupled with an HPV-QUEST genotyping server and a bioinformatic pipeline, was established and applied to survey the diversity of HPV genotypes among a subset of healthy men from the HPV in Men (HIM) Multinational Study. Twenty-one HPV genotypes (12 high-risk and 9 low-risk) were detected in the genital area from 18 asymptomatic individuals. A single HPV type, either HPV16, HPV6b or HPV83, was detected in 7 individuals, while coinfection by 2 to 5 high-risk and/or low-risk genotypes was identified in the other 11 participants. In two individuals studied for over one year, HPV16 persisted, while fluctuations of coinfecting genotypes occurred. HPV L1 regions were generally identical between query and reference sequences, although nonsynonymous and synonymous nucleotide polymorphisms of HPV16, 18, 31, 35h, 59, 70, 73, cand85, 6b, 62, 81, 83, cand89 or JEB2 L1 genotypes, mostly unidentified by linear array, were evident. Deep sequencing coupled with HPV-QUEST provides efficient and unambiguous classification of HPV genotypes in multiple-type HPV infection in host ecosystems.
多种类型的人乳头瘤病毒(HPV)感染在无症状个体中持续存在的风险更大,并且可能加速癌症发展。为了扩大基于探针检测所定义的HPV类型范围,建立了HPV L1多重深度测序,并结合HPV-QUEST基因分型服务器和生物信息学流程,将其应用于来自男性HPV(HIM)多国研究的一部分健康男性中,以调查HPV基因型的多样性。在18名无症状个体的生殖器区域检测到21种HPV基因型(12种高危型和9种低危型)。7名个体检测到单一HPV类型,即HPV16、HPV6b或HPV83,而在其他11名参与者中鉴定出2至5种高危和/或低危基因型的合并感染。在两名研究超过一年的个体中,HPV16持续存在,同时合并感染的基因型出现波动。尽管HPV16、18、31、35h、59、70、73、cand85、6b、62、81、83、cand89或JEB2 L1基因型的非同义及同义核苷酸多态性大多未被线性阵列识别,但HPV L1区域在查询序列和参考序列之间通常是相同的。深度测序结合HPV-QUEST可对宿主生态系统中多种类型HPV感染的HPV基因型进行高效且明确的分类。