Whole exome sequencing identifies genetic markers of enterovirus susceptibility in East Asians

被引:0
|
作者
Sung, Chia-Cheng [1 ]
Luxton, G. W. Gant [2 ]
Hung, Kuo-Sheng [3 ]
Wu, Yung-Fu [3 ]
Wang, Chih-Chien [1 ]
Hsu, Chih-Sin [4 ]
Hu, Chih-Fen [1 ]
机构
[1] Triserv Gen Hosp, Natl Def Med Ctr, Dept Pediat, Taipei, Taiwan
[2] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA USA
[3] Tri Serv Gen Hosp, Ctr Precis Med & Genom, Natl Def Med Ctr, Taipei, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Genom Ctr Clin & Biotechnol Applicat, Canc Progress Res Ctr, Taipei, Taiwan
关键词
enterovirus; enterovirus infection with severe complications; whole exome sequencing; genetic signature; East Asian population; PATHOGENESIS; INFECTIONS;
D O I
10.3389/fmicb.2024.1452595
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Introduction Following acute enterovirus (EV) infection, outcomes vary based on factors like the immune response, viral cell entry receptor expression levels, tissue tropism, and genetic factors of both the host and virus. While most individuals exhibit mild, self-limited symptoms, others may suffer severe complications or prolonged infections that can lead to autoimmune disorders.Methods To elucidate host responses to EV infection, we performed whole exome sequencing on blood samples from both infected and uninfected individuals. Our initial focus was on genes encoding EV entry receptors-PSGL-1, SCARB2, and ANAXA2 for EV-A71, and CD155 for poliovirus-and on host genes ACBD3 and PI4K Beta, crucial for EV replication.Results Although no specific genetic variants directly associated with EV infection were identified, we discovered 118 variants across 116 genes enriched in East Asian populations through multi-layered variant filtering. These variants were further analyzed for their potential impacts on organs, biological processes, and molecular pathways. Phenome-wide association studies were conducted to refine our understanding of their contributions to EV infection susceptibility.Discussion Our findings aim to develop a predictive panel based on these 118 variants, which could help susceptible individuals during EV outbreaks, guiding targeted clinical interventions and preventative strategies.
引用
收藏
页数:13
相关论文
共 50 条
  • [31] Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms
    Maegawa, Tatsuya
    Akagawa, Hiroyuki
    Onda, Hideaki
    Kasuya, Hidetoshi
    PLOS ONE, 2022, 17 (03):
  • [32] Whole-exome sequencing identifies susceptibility genes and pathways for idiopathic pulmonary fibrosis in the Chinese population
    Chuling Fang
    Hui Huang
    Yujia Feng
    Qian Zhang
    Na Wang
    Xiaoyan Jing
    Jian Guo
    Martin Ferianc
    Zuojun Xu
    Scientific Reports, 11
  • [33] Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility
    Shannon Bruse
    Michael Moreau
    Yana Bromberg
    Jun-Ho Jang
    Nan Wang
    Hongseok Ha
    Maria Picchi
    Yong Lin
    Raymond J. Langley
    Clifford Qualls
    Julia Klesney-Tait
    Joseph Zabner
    Shuguang Leng
    Jenny Mao
    Steven A. Belinsky
    Jinchuan Xing
    Toru Nyunoya
    Human Genomics, 10
  • [34] Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility
    Bruse, Shannon
    Moreau, Michael
    Bromberg, Yana
    Jang, Jun-Ho
    Wang, Nan
    Ha, Hongseok
    Picchi, Maria
    Lin, Yong
    Langley, Raymond J.
    Qualls, Clifford
    Klensney-Tait, Julia
    Zabner, Joseph
    Leng, Shuguang
    Mao, Jenny
    Belinsky, Steven A.
    Xing, Jinchuan
    Nyunoya, Toru
    HUMAN GENOMICS, 2016, 10
  • [35] Whole-exome sequencing identifies variants associated with structural MRI markers in patients with bipolar disorders
    Han, Mi-Ryung
    Han, Kyu-Man
    Kim, Aram
    Kang, Wooyoung
    Kang, Youbin
    Kang, June
    Won, Eunsoo
    Tae, Woo-Suk
    Cho, Yunjung
    Ham, Byung-Joo
    JOURNAL OF AFFECTIVE DISORDERS, 2019, 249 : 159 - 168
  • [36] Whole Exome Sequencing Identifies Damaging Variants in Indonesians with Clefts
    Aladenika, Emmanuel
    Maskoen, Ani
    Awotoye, Waheed
    Abdulaziz, Rasyid
    Alade, Azeez
    Nasroen, Saskia Lenggogeni
    Oladayo, Abimbola
    Busch, Tamara
    Sarilita, Erli
    Butali, Azeez
    CLEFT PALATE CRANIOFACIAL JOURNAL, 2023,
  • [37] Exome sequencing identifies genetic variants in anophthalmia and microphthalmia
    Li, Jingjing
    Yang, Wei
    Wang, Yuejun Jessie
    Ma, Chen
    Curry, Cynthia J.
    McGoldrick, Daniel
    Nickerson, Deborah A.
    Chong, Jessica X.
    Blue, Elizabeth E.
    Mullikin, James C.
    Reefhuis, Jennita
    Nembhard, Wendy N.
    Romitti, Paul A.
    Werler, Martha M.
    Browne, Marilyn L.
    Olshan, Andrew F.
    Finnell, Richard H.
    Feldkamp, Marcia L.
    Pangilinan, Faith
    Almli, Lynn M.
    Bamshad, Mike J.
    Brody, Lawrence C.
    Jenkins, Mary M.
    Shaw, Gary M.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2022, 188 (08) : 2376 - 2388
  • [38] Whole exome sequencing identifies mutational signatures of vitreoretinal lymphoma
    Lee, Junwon
    Kim, Borahm
    Lee, Hyeonah
    Park, Heejung
    Byeon, Suk Ho
    Choi, Jong Rak
    Lee, Sung Chul
    Lee, Seung-Tae
    Lee, Christopher Seungkyu
    HAEMATOLOGICA, 2020, 105 (09) : E458 - E460
  • [39] Whole exome sequencing analysis identifies genes for alcohol consumption
    Kang, Jujiao
    Deng, Yue-Ting
    Wu, Bang-Sheng
    Liu, Wei-Shi
    Li, Ze-Yu
    Xiang, Shitong
    Yang, Liu
    You, Jia
    Gong, Xiaohong
    Jia, Tianye
    Yu, Jin-Tai
    Cheng, Wei
    Feng, Jianfeng
    NATURE COMMUNICATIONS, 2024, 15 (01)
  • [40] Whole Exome Sequencing Identifies Novel Variants and Pathways in Neurodegeneration
    Ahmeti, Kreshnik B.
    Yang, Jianhua
    Fecto, Faisal W.
    Kinsley, Lisa M.
    Siddique, Nailah A.
    Pericak-Vance, Margaret A.
    Hann-Xiang, Deng
    Ma, Yong-Chao
    Siddique, Teepu
    ANNALS OF NEUROLOGY, 2015, 78 : S113 - S113