4.7 Article

Characterization of Coxsackievirus A6 Strains Isolated From Children With Hand, Foot, and Mouth Disease

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2021.700191

Keywords

Coxsackievirus A6; HFMD; KMB17 cell-adapted strain; biological characteristic; vaccine

Funding

  1. Research Projects of Yunnan Province, China [20200AA100009, 2017FA006]
  2. CAMS Innovation Fund for Medical Sciences (CIFMS) [2016-I2M-1-019, 2016-I2M-3-026]
  3. Yunnan Leading Medical Scientist Training Program [L-2018003]

Ask authors/readers for more resources

CVA6 is a key pathogen causing hand, foot and mouth disease, and the KYN-A1205 strain adapted to KMB17 cells shows stronger virulence, virus tropism, and immunogenicity, making it a potential vaccine candidate.
Coxsackievirus A6 (CVA6) is a key pathogen causing hand, foot and mouth disease (HFMD). However, there are currently no specific antiviral drugs or vaccines for treating infections caused by CVA6. In this study, human rhabdomyosarcoma (RD), African green monkey kidney (Vero), and human embryonic lung diploid fibroblast (KMB17) cells were used to isolate CVA6 from 327 anal swab and fecal samples obtained during HFMD monitoring between 2009 and 2017. The VP1 genes of the isolates were sequenced and genotyped, and the biological characteristics of the representative CVA6 strains were analyzed. A total of 37 CVA6 strains of the D3 gene subtypes were isolated from RD cells, all of which belonged to the epidemic strains in mainland China. Using the adaptive culture method, 10 KMB17 cell-adapted strains were obtained; however, no Vero cell-adapted strains were acquired. Among the KMB17 cell-adapted strains, only KYN-A1205 caused disease or partial death in suckling mice, and its virulence was stronger than its RD cell-adapted strain. The pathogenic KYN-A1205 strain caused strong tropism to the muscle tissue and led to pathological changes, including muscle necrosis and nuclear fragmentation in the forelimb and hindlimb. Sequence analysis demonstrated that the KYN-A1205 strain exhibited multiple amino acid mutations after KMB17 cell adaptation. Moreover, it showed strong pathogenicity, good immunogenicity and genetic stability, and could be used as an experimental CVA6 vaccine candidate.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available