Diversity and Evolutionary Histories of Human Coronaviruses NL63 and 229E Associated with Acute Upper Respiratory Tract Symptoms in Kuala Lumpur, Malaysia

被引:12
|
作者
Al-Khannaq, Maryam Nabiel [1 ]
Kim Tien Ng [1 ]
Oong, Xiang Yong [1 ]
Pang, Yong Kek [1 ]
Takebe, Yutaka [1 ,2 ,3 ]
Chook, Jack Bee [1 ,4 ]
Hanafi, Nik Sherina [5 ]
Kamarulzaman, Adeeba [1 ]
Tee, Kok Keng [6 ]
机构
[1] Univ Malaya, Dept Med, Fac Med, Kuala Lumpur, Malaysia
[2] Natl Inst Infect Dis, AIDS Res Ctr, Shinjuku Ku, Tokyo, Japan
[3] Yokohama City Univ, Sch Med, Yokohama, Kanagawa, Japan
[4] Management & Sci Univ, Dept Hlth Sci, Fac Hlth & Life Sci, Selangor, Malaysia
[5] Univ Malaya, Dept Primary Care Med, Fac Med, Kuala Lumpur, Malaysia
[6] Univ Malaya, Dept Med Microbiol, Fac Med, Kuala Lumpur 50603, Malaysia
来源
关键词
FREQUENT DETECTION; COMMON COLD; INFECTIONS; SPIKE; CHILDREN; SEQUENCE; VIRUSES; HKU1; IDENTIFICATION; GENES;
D O I
10.4269/ajtmh.15-0810
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The human alphacoronaviruses HCoV-NL63 and HCoV-229E are commonly associated with upper respiratory tract infections (URTI). Information on their molecular epidemiology and evolutionary dynamics in the tropical region of southeast Asia however is limited. Here, we analyzed the phylogenetic, temporal distribution, population history, and clinical manifestations among patients infected with HCoV-NL63 and HCoV-229E. Nasopharyngeal swabs were collected from 2,060 consenting adults presented with acute URTI symptoms in Kuala Lumpur, Malaysia, between 2012 and 2013. The presence of HCoV-NL63 and HCoV-229E was detected using multiplex polymerase chain reaction (PCR). The spike glycoprotein, nucleocapsid, and 1a genes were sequenced for phylogenetic reconstruction and Bayesian coalescent inference. A total of 68/2,060 (3.3%) subjects were positive for human alphacoronavirus; HCoV-NL63 and HCoV-229E were detected in 45 (2.2%) and 23 (1.1%) patients, respectively. A peak in the number of HCoV-NL63 infections was recorded between June and October 2012. Phylogenetic inference revealed that 62.8% of HCoV-NL63 infections belonged to genotype B, 37.2% was genotype C, while all HCoV-229E sequences were clustered within group 4. Molecular dating analysis indicated that the origin of HCoV-NL63 was dated to 1921, before it diverged into genotype A (1975), genotype B (1996), and genotype C (2003). The root of the HCoV-229E tree was dated to 1955, before it diverged into groups 1-4 between the 1970s and 1990s. The study described the seasonality, molecular diversity, and evolutionary dynamics of human alphacoronavirus infections in a tropical region.
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收藏
页码:1058 / 1064
页数:7
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