1.Disseminated herpes zoster in immunocompetent patients not due to varicella-zoster virus gene mutation.
Zhong-hui SUN ; Yun-yi GUO ; Ming LI ; Zhi-rong YAO
Chinese Medical Journal 2013;126(16):3193-3193
Adult
;
Herpes Zoster
;
etiology
;
Herpesvirus 3, Human
;
genetics
;
Humans
;
Male
;
Middle Aged
;
Mutation
2.Genomic structure of varicella-zoster virus and its vaccine application status.
Jing Bo TAO ; Bin Bin WAN ; Jin Hua CHEN ; Jian Wei JIA ; Hang CHENG ; Ling Qiao LOU ; Shu Ying LUO
Chinese Journal of Preventive Medicine 2023;57(2):286-292
With the determination of the whole genome sequence of varicella-zoster virus (VZV) virus, the successful breakthrough of infectious cloning technology of VZV, and the emergence of effective preventive vaccines, which have been proven to be effective and safe, varicella has become a disease preventable by specific immunity. This article will review the genomic structure, epidemiological characteristics, and research application progress of varicella vaccine and herpes zoster vaccine of varicella zoster virus to provide reference for primary prevention of the disease.
Humans
;
Herpesvirus 3, Human/genetics*
;
Herpes Zoster/prevention & control*
;
Herpes Zoster Vaccine
;
Chickenpox Vaccine
;
Genomics
3.Analysis on the epidemic characteristics and genetic characteristics of varicella in Beijing from 2019 to 2021.
Ai Hua LI ; Dan ZHAO ; Xiao Jing WEN ; Fang HUANG ; Li LU ; Meng CHEN ; Cheng GONG
Chinese Journal of Preventive Medicine 2022;56(8):1118-1122
The reported incidence of varicella in Beijing from 2019 to 2021 were 63.8/100 000, 32.2/100 000 and 38.6/100 000, respectively. There were two VZV epidemics in Beijing each year, one peaked in May and the other in November. However, the first VZV epidemic almost disappeared in 2020. Among the cases involved in the varicella outbreaks in school, the proportion of the students with no history of vaccine immunization, 1 dose of immunization and 2 doses of immunization were 33.12%, 44.79% and 22.08%, respectively. The major body of VZV breakthrough cases was children aged 6-14 years (523/755, 69.27%). The proportion of moderate- or severe-rash were 55.32%, 39.06%, 29.96% in the three groups of cases with no immunization history, 1 dose of immunization and 2 doses of immunization, respectively (P<0.001). A total of 1 089 varicella samples were collected, and 837 (76.86%) were confirmed to be PCR-positive for VZV and were identified as VZV wild strains. 311 VZV strains were sequenced successfully, and 307 strains were clade 2 (98.72%), 1 clade 3 (0.32%) and 3 Clade 5 (0.96%). Compared with the representative strains, the nucleotide similarities of ORF22 fragments were between 99.4% and 100%, and amino acid similarities were between 99.4% and 100%.
Beijing/epidemiology*
;
Chickenpox/epidemiology*
;
Chickenpox Vaccine
;
Child
;
Herpesvirus 3, Human/genetics*
;
Humans
;
Schools
;
Vaccination
4.Genetic characteristics of varicella zoster virus in Shandong province from 2020 to 2021.
Meng CHEN ; Su Ting WANG ; Yao LIU ; Ping XIONG ; Ze Xin TAO ; Li ZHANG ; Jin Li JIA ; Chang Yin WANG ; Songtao XU
Chinese Journal of Preventive Medicine 2022;56(8):1080-1086
Objective: To investigate the genetic characteristics of varicella zoster virus (VZV) in Shandong province from 2020 to 2021. Methods: From April 2020 to December 2021, 85 herpes fluid samples from suspected varicella patients in Shandong province were collected. The qPCR was used to detect viral DNA and screen suspected samples. Six single nucleotide polymorphisms (SNPs) of ORF22 fragment and ORF38 fragment in positive samples were examined via PCR and Sanger sequencing to identify the viral genotypes. Four SNPs of ORF38 and ORF62 were examined to identify the vaccine and wild-type strains. The sequences were analyzed with Sequencher and MEGA7 software, using the VZV reference strain sequences from GenBank. Results: In the 85 samples suspected of varicella, 80 were VZV positive and wild-type strains belonging to Clade 2. Compared with clade 2 representative strains, the nucleotide and amino acid similarities of ORF22 fragment were 99.5%-100% and 98.5%-100%, respectively. SD20-1, SD20-5, SD20-6, SD20-8, SD20-9, SD20-10, SD20-11, SD20-12, SD20-13, SD20-30 and SD20-31 had a A➝G nucleotide mutation at 37990, causing amino acid change from glutamine to arginine. SD21-1 had a C➝A nucleotide mutation at 38059, causing threonine to asparagine during coding. Conclusions: From 2020 to 2021, all VZV strains in Shandong province are the wild-type strains belonging to Clade 2.
Amino Acids/genetics*
;
Chickenpox
;
Chickenpox Vaccine/genetics*
;
Herpes Zoster
;
Herpesvirus 3, Human/genetics*
;
Humans
;
Nucleotides
;
Polymorphism, Single Nucleotide
;
Real-Time Polymerase Chain Reaction
5.The genotyping and molecular evolution of varicella-zoster virus.
Long-Feng JIANG ; Lin GAN ; Jing-Xian CHEN ; Ming-Li WANG
Chinese Journal of Virology 2012;28(5):584-590
Varicella-zoster virus (VZV, Human herpesvirus 3) is a member of the family Herpesviridae, and is classified as alpha-subfamily along with HSV-1 and HSV-2. VZV is the causative agent of chicken pox (varicella) mostly in children, after which it establishes latency in the sensory ganglia with the potential to reactivate at a later time to cause shingles (zoster). Increasing molecular epidemiological studies in recent years have been performed to monitor the mutations in VZV genome, discriminate vaccine virus from wild type virus, study the phylogeny of VZV strains throughout the world, and understand the evolution of the different clades of VZV. The progress has great impact on the fields of epidemiology, virology and bioinformatics. In this review, the currently available data concerning the geographic distribution and molecular evolution of VZV clades are discussed.
Animals
;
Base Sequence
;
Evolution, Molecular
;
Genotype
;
Herpes Zoster
;
virology
;
Herpesvirus 3, Human
;
classification
;
genetics
;
isolation & purification
;
Humans
;
Molecular Sequence Data
;
Phylogeny
6.Correlation of EBV Infection with Expression of TNF-α-Inducing Protein 3 Gene and A20 Protein in Hodgkin's Lmphoma.
Yu-Xiu XU ; Dong-Sheng MA ; Meng XU ; Jing YANG
Journal of Experimental Hematology 2019;27(1):91-95
OBJECTIVE:
To analyze the correlation of EBV infection with expression of TNF-α-inducing protein 3 gene and A20 protein in Hodgkin lmphoma.
METHODS:
The clinical data and pathological specimens of 65 cases of Hodgkin's lymphoma in our hospital were analyzed retrospectively, and the tissue chips were made for the rich area of the tumor cells. The latent membrane protein 1 encoded by EBV was measured by immunohistochemical staining, and the RNA encoded by EBV was measured by in situ hybridization to analyze the infection state. The gene expression of tumor necrosis factor.α-induced protein 3 was detected by fluorescence in situ hybridization, and the expression of A20 protein encoded by EBV was detected by immunohistochemical staining. The obtained data were processed by SPSS 23.0 version statistical software.
RESULTS:
The positive rate of latent membrane protein 1 was 26.15% (17/65), the positive rate of EBV encoded RNA was 26.15% (17/65), and the coincidence rate was 100.00%. In 65 patients, A20 protein expression was lost in 18 cases (27.69%), and 14 cases (21.54%) showed homozygous or heterozygous deletion of tumor necrosis factorα protein 3 gene. Only 1 case showed A20 loss combined with homozygous deletion of TNFα inducible protein 3. Correlation analysis showed that EBV infection did not significantly relate with expression loss of A20 protein and the gene deletion of TNF-α inducing protein 3 (P>0.05).
CONCLUSION
The expression loss of A20 protein and gene detection of TNFα inducing protein 3 are found in both EBV negative and positive patients with Hodgkin's lymphoma, however the results of immunohistochemical staining and fluorescence in situ hybridization are not complete consistant, the reason may closely relate with the technical factors.
Epstein-Barr Virus Infections
;
Herpesvirus 4, Human
;
Hodgkin Disease
;
Humans
;
In Situ Hybridization
;
In Situ Hybridization, Fluorescence
;
Retrospective Studies
;
Tumor Necrosis Factor alpha-Induced Protein 3
;
genetics
;
Viral Matrix Proteins
7.Genetic characterization of varicella-zoster virus in people aged 20 years and under in Yichang City of Hubei Province, 2019-2020.
Mei Ying YOU ; Miao Miao WANG ; Hong GUO ; Tian Qi WANG ; Xu Dong LI ; Song Tao XU ; Yue Hua HU ; Da Ping YIN
Chinese Journal of Epidemiology 2023;44(4):607-610
Objective: To analyze the genetic characteristics of varicella-zoster virus (VZV) in people aged 20 years and under in Yichang City of Hubei Province from 2019 to 2020. Methods: Based on the Yichang Health Big Data Platform, we investigated cases 20 and under clinically diagnosed as herpes zoster in three hospitals from March 2019 to September 2020. Collecting vesicle fluid and throat swab samples of the cases and completing questionnaires to obtain basic information. Real-time fluorescent quantitative PCR was used for positive identification of the virus. PCR amplification of VZV's open reading frame (ORF) and sequencing of the products to determine the VZV genotype. Analyze mutations at some specific single nucleotide polymorphism (SNP) sites. Results: Among 46 cases of herpes zoster, the male to female ratio was 1.3∶1 (26∶20) and the age ranged from 7 to 20 years old. Fifteen cases had been vaccinated against varicella, including 13 and 2 cases of 1 and 2 doses, respectively. VZV strains were detected in 34 samples (73.91%), all belonging to Clade 2. Phylogenetic tree analysis of the nucleotide of ORF22 showed, compared with Clade 2 referenced strains, the sequence matching degree of nucleotide for all 34 samples was 99.0% to 100.0%. Conclusion: The main VZV strain causing herpes zoster in people aged 20 years and under in Yichang from 2019 to 2020 was Clade 2.
Humans
;
Child
;
Adolescent
;
Young Adult
;
Adult
;
Herpesvirus 3, Human/genetics*
;
Phylogeny
;
Herpes Zoster/epidemiology*
;
Polymorphism, Single Nucleotide
;
Real-Time Polymerase Chain Reaction
;
Nucleotides
8.Sequence analysis of varicella-zoster virus gE gene in varicella-zoster virus strains with different clades.
Long-Feng JIANG ; Lin GAN ; Shan-Shan LI ; Yan-Yan FENG ; Wei JIANG ; Ya-ping DUAN ; Jing-Xian CHEN ; Ming-Li WANG
Chinese Journal of Virology 2013;29(2):112-118
To analyze the gE gene sequence of varicella-zoster virus (VZV) strains of different clades and subclades currently circulating in China. Eighteen skin lesion fluid swabs or skin scab pieces from patients with chickenpox or shingles were obtained from Beijing, Changchun, Lhasa and Urumqi between December 2010 and June 2011. The genotype of the virus strains was determined by a group of single nucleotide polymorphism (SNP) located in 15 ORFs, and the full-length gE genes of 18 strains representing all the clades in the study was amplified by PCR and sequenced. In addition to the synonymous mutations and non-synonymous mutations that were reported in the literature, there were 3 novel non-synonymous mutations (C56T, C1109T, C917A) and 4 new synonymous mutations (C54T, T1075C, T816C, G279A) found in the 8 strains analyzed. We found the VZV strains of clade 5 in Xinjiang for the first time,and the genotypes of some VZV strains circulating in Chagnchun could not be determined by the present methods. The analysis of gE gene sequences,revealed a novel non-synonymous mutations in the e1 and c1 epitopes, corresponding to the amino acid change of serine to tyrosine.
Adolescent
;
Adult
;
Aged
;
Base Sequence
;
Chickenpox
;
virology
;
Child
;
China
;
Female
;
Genotype
;
Herpesvirus 3, Human
;
classification
;
genetics
;
Humans
;
Male
;
Middle Aged
;
Molecular Sequence Data
;
Mutation, Missense
;
Open Reading Frames
;
Sequence Analysis, DNA
;
Viral Envelope Proteins
;
genetics
;
Viral Proteins
;
genetics
;
Young Adult