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Nationwide distribution of varicella-zoster virus clades in China.

Nationwide distribution of varicella-zoster virus clades in China.
Author Information (click to view)

Xu S, Chen M, Zheng H, Wang H, Chen M, Zhou J, Shuang W, Yu P, Ma C, He J, Feng D, Zhen Z, Yan Z, Naiying M, Cui A, Wu Q, Qi M, Li C, Xu X, Xu W,


Xu S, Chen M, Zheng H, Wang H, Chen M, Zhou J, Shuang W, Yu P, Ma C, He J, Feng D, Zhen Z, Yan Z, Naiying M, Cui A, Wu Q, Qi M, Li C, Xu X, Xu W, (click to view)

Xu S, Chen M, Zheng H, Wang H, Chen M, Zhou J, Shuang W, Yu P, Ma C, He J, Feng D, Zhen Z, Yan Z, Naiying M, Cui A, Wu Q, Qi M, Li C, Xu X, Xu W,

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BMC infectious diseases 2016 Oct 716(1) 542
Abstract
BACKGROUND
In 2010, a universal nomenclature for varicella-zoster virus (VZV) clades was established, which is very useful in the monitoring of viral evolution, recombination, spread and genetic diversity. Currently, information about VZV clades has been disclosed worldwide, however, there are limited data regarding the characterization of circulating VZV clades in China, even where varicella remains widely epidemic.

METHODS
From 2008 to 2012, clinical samples with varicella or zoster were collected in General Hospital in eight provinces and analyzed by PCR, restriction endonuclease digestion and sequencing. The viral clades were determined by analysis of five single nucleotide polymorphisms (SNPs) within the 447-bp fragment of open reading frame (ORF) 22, and the restriction fragment length polymorphisms (RFLPs) of ORF 38 (PstI), ORF 54 (BglI) and ORF 62 (SmaI) were evaluated to understand genetic diversity of VZV and determinate varicella vaccine adverse event (VVAE).

RESULTS
Seventy-seven varicella and 11 zoster samples were identified as being positive for VZV. The five SNPs profile showed that the majority of VZV strains belonged to clade 2, but clade 5 and clade 4 strains were also found in Guangdong. The RFLPs analysis of the DNA fragments of ORF 38, 54 and 62 showed that 85 of these samples were characterized as PstI + BglI + SamI-, and the remaining three VZV strains from varicella patients were characterized as PstI-BglI + SamI+ which is the genetic profile of VVAEs.

CONCLUSIONS
The study suggested that the predominant clade 2 VZVs had been continually circulating since at least the 1950s in China. Nearly all VZV strains except VVAEs possessed the genetic profile of PstI + BglI + Sam-. However, the other clades were also found to be co-circulating with clade 2, especially in the border regions. These results highlighted the need for the constant and broad use of virologic surveillance to provide an important genetic baseline for varicella control and vaccination programs in China.

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