Wu Xiaowei, Zhang Jing, Lan Wendong, Quan Lulu, Ou Junxian, Zhao Wei, Wu Jianguo, Woo Patrick C Y, Seto Donald, Zhang Qiwei
BSL-3 Laboratory, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, China.
Guangdong Provincial Key Laboratory of Virology, Institute of Medical Microbiology, Jinan University, Guangzhou, China.
Front Microbiol. 2022 May 12;13:911694. doi: 10.3389/fmicb.2022.911694. eCollection 2022.
Human adenoviruses (HAdVs) within species B, C, and E are responsible for highly contagious and potentially severe respiratory disease infections. The traditional method to type these pathogens was based on virus neutralization and hemagglutination assays, which are both time-consuming and difficult, particularly due to the nonavailability of reagents. Subsequent molecular typing based on the partial characterization of the hexon gene and/or the restriction enzyme analysis (REA) of the genomes is inadequate, particularly in identifying recombinants. Here, a rapid, simple, and cost-effective method for molecular typing HAdV respiratory pathogens is presented. This incorporates three pairs of universal PCR primers that target the variable regions of the three major capsid genes, i.e., hexon, penton base, and fiber genes, that span the genome. The protocol enables typing and characterization of genotypes within species B, C, and E, as well as of some genotypes within species D and F. To validate this method, we surveyed 100 children with HAdV-associated acute respiratory infections identified by direct immunofluorescence (Hong Kong; July through October, 2014). Throat swab specimens were collected and analyzed by PCR amplification and sequencing; these sequences were characterized by BLAST. HAdVs were detected in 98 out of 100 (98%) samples, distributing as follows: 74 HAdV-B3 (74%); 10 HAdV-E4 (10%); 7 HAdV-C2 (7%); 2 HAdV-C6 (2%); 1 HAdV-B7 (1%); 1 HAdV-C1 (1%); 2 co-infection (2%); and 1 novel recombinant (1%). This study is the first detailed molecular epidemiological survey of HAdVs in Hong Kong. The developed method allows for the rapid identification of HAdV respiratory pathogens, including recombinants, and bypasses the need for whole genome sequencing for real-time surveillance of circulating adenovirus strains in outbreaks and populations by clinical virologists, public health officials, and epidemiologists.
B、C和E种的人类腺病毒(HAdVs)可导致具有高度传染性且可能严重的呼吸道疾病感染。对这些病原体进行分型的传统方法基于病毒中和试验和血凝试验,这两种方法都既耗时又困难,尤其是由于试剂难以获得。随后基于六邻体基因部分特征和/或基因组的限制性酶切分析(REA)的分子分型并不充分,特别是在鉴定重组体方面。在此,我们提出一种快速、简单且经济高效的对HAdV呼吸道病原体进行分子分型的方法。该方法包含三对通用PCR引物,靶向三个主要衣壳基因的可变区,即跨越基因组的六邻体、五邻体基座和纤维基因。该方案能够对B、C和E种内的基因型以及D和F种内的一些基因型进行分型和特征描述。为验证该方法,我们调查了100名经直接免疫荧光法确诊为HAdV相关急性呼吸道感染的儿童(香港;2014年7月至10月)。采集咽拭子标本,通过PCR扩增和测序进行分析;这些序列通过BLAST进行特征描述。100个样本中有98个(98%)检测到HAdVs,分布如下:74个HAdV-B3(74%);10个HAdV-E4(10%);7个HAdV-C2(7%);2个HAdV-C6(2%);1个HAdV-B7(1%);1个HAdV-C1(1%);2个共感染(2%);以及1个新型重组体(1%)。本研究是香港首次对HAdVs进行的详细分子流行病学调查。所开发的方法能够快速鉴定HAdV呼吸道病原体,包括重组体,并且临床病毒学家、公共卫生官员和流行病学家在对疫情爆发和人群中传播的腺病毒株进行实时监测时无需进行全基因组测序。