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Rubella is listed as a disease that needs to be eliminated worldwide by the World Health Organization. This study aimed to investigate rubella epidemiology and genetic characteristics based on data from 12 years of laboratory‐based surveillance (2009–2020) in Tianjin and to provide baseline genotype data for monitoring future rubella control efforts. We collected RV‐positive throat swab samples from confirmed rubella cases during 2009–2020 in Tianjin to isolate RV, amplify and sequence target gene fragments, construct phylogenetic trees, and analyze nucleotide homologies. Four rubella isolates were chosen for whole genome sequencing. The epidemiological data of rubella cases were collected to describe and analyze the epidemiological characteristics of the rubella outbreak. Most cases (87.6%) occurred between March and June, and the peak incidence was observed in May. The age of the reported rubella cases ranged from almost 1 month to 82 years, most were between 10 and 29 years old (83.3%). Almost half (48.3%) of the confirmed rubella cases were from just four districts (Beichen District, Binhai New Area, Hebei District, and Nankai District). A total of 211 rubella virus strains were obtained during 2009–2020, phylogenetic analyses identified four lineages, including 1E‐L1, 1E‐L2, 2B‐L1, and 2B‐L2c, with high homologies of nucleotide sequences compared with RV strains from other provinces of China. Recombination analysis indicated that strain RVi/Tianjin.CHN/37.19/1 a possible recombination strain by 7 analysis methods, with p‐values of 4.993 × 10−28–2.922 × 10−4. Our study provided comprehensive data on rubella epidemiology and the first information on rubella genotypes in Tianjin. Clear evidence of recombination was found, indicating that RV has the potential to continually mutate, so close monitoring of the genetic variations of wild‐type rubella virus strains is necessary. Rubella viruses were highly conserved at the genomic level, the incidence of rubella in Tianjin, as well as in China, has sustains at a low level, which gives us the idea that the rubella control and elimination goal could be achieved in the near future if strengthened RV surveillance continues and vaccine immunization coverage maintaining at the high level.
Rubella is listed as a disease that needs to be eliminated worldwide by the World Health Organization. This study aimed to investigate rubella epidemiology and genetic characteristics based on data from 12 years of laboratory‐based surveillance (2009–2020) in Tianjin and to provide baseline genotype data for monitoring future rubella control efforts. We collected RV‐positive throat swab samples from confirmed rubella cases during 2009–2020 in Tianjin to isolate RV, amplify and sequence target gene fragments, construct phylogenetic trees, and analyze nucleotide homologies. Four rubella isolates were chosen for whole genome sequencing. The epidemiological data of rubella cases were collected to describe and analyze the epidemiological characteristics of the rubella outbreak. Most cases (87.6%) occurred between March and June, and the peak incidence was observed in May. The age of the reported rubella cases ranged from almost 1 month to 82 years, most were between 10 and 29 years old (83.3%). Almost half (48.3%) of the confirmed rubella cases were from just four districts (Beichen District, Binhai New Area, Hebei District, and Nankai District). A total of 211 rubella virus strains were obtained during 2009–2020, phylogenetic analyses identified four lineages, including 1E‐L1, 1E‐L2, 2B‐L1, and 2B‐L2c, with high homologies of nucleotide sequences compared with RV strains from other provinces of China. Recombination analysis indicated that strain RVi/Tianjin.CHN/37.19/1 a possible recombination strain by 7 analysis methods, with p‐values of 4.993 × 10−28–2.922 × 10−4. Our study provided comprehensive data on rubella epidemiology and the first information on rubella genotypes in Tianjin. Clear evidence of recombination was found, indicating that RV has the potential to continually mutate, so close monitoring of the genetic variations of wild‐type rubella virus strains is necessary. Rubella viruses were highly conserved at the genomic level, the incidence of rubella in Tianjin, as well as in China, has sustains at a low level, which gives us the idea that the rubella control and elimination goal could be achieved in the near future if strengthened RV surveillance continues and vaccine immunization coverage maintaining at the high level.
Coxsackievirus A4 (CVA4) has recently become one of the most common causative agents of hand, foot, and mouth disease. The current study investigated the genetic diversity and spread of recombinant CVA4 by analyzing circulating genotypes and recombinant strains in Bangkok, Thailand, from 2017 to 2023. Partial VP1, 3Dpol, and whole genome sequencing of CVA4 samples collected from collaborating hospitals were conducted. Phylogenetic analysis of CVA4 VP1 and 3Dpol genome regions revealed discordance, indicating recombination. The predominant CVA4 genotype was C3, primarily observed in 2019. The predominant genotype in 2017 was C1. D2, commonly found in China, was occasionally observed. In nucleotide similarity analysis, intertypic recombination between CVA4 and EV-A during the evolutionary history of the virus was evident, particularly in the nonstructural region. The estimated emergence of genotypes C1 and C3 in Thailand occurred around 2014, with an evolutionary rate of 5.8 × 10 − 3 nucleotide substitutions per site per year. Genotype D2 exhibited notable variability across both the entire genome and the structural protein region compared to genotype C. Monitoring the genetic diversity and circulation of recombinant CVA4 is crucial for identifying newly emerging virus strains, enabling prompt public health responses and containment efforts, and enhancing surveillance in Thailand. Supplementary Information The online version contains supplementary material available at 10.1038/s41598-024-77832-6.
Background Hand, foot, and mouth disease (HFMD) is a global public health concern, notably within the Asia-Pacific region. Recently, the primary pathogen causing HFMD outbreaks across numerous countries, including China, is coxsackievirus (CV) A6, one of the most prevalent enteroviruses in the world. It is a new variant that has undergone genetic recombination and evolution, which might not only induce modifications in the clinical manifestations of HFMD but also heighten its pathogenicity because of nucleotide mutation accumulation. Objective The study assessed the epidemiological characteristics of HFMD in China and characterized the molecular epidemiology of the major pathogen (CV-A6) causing HFMD. We attempted to establish the association between disease progression and viral genetic evolution through a molecular epidemiological study. Methods Surveillance data from the Chinese Center for Disease Control and Prevention from 2021 to 2023 were used to analyze the epidemiological seasons and peaks of HFMD in Henan, China, and capture the results of HFMD pathogen typing. We analyzed the evolutionary characteristics of all full-length CV-A6 sequences in the NCBI database and the isolated sequences in Henan. To characterize the molecular evolution of CV-A6, time-scaled tree and historical population dynamics regarding CV-A6 sequences were estimated. Additionally, we analyzed the isolated strains for mutated or missing amino acid sites compared to the prototype CV-A6 strain. Results The 2021-2023 epidemic seasons for HFMD in Henan usually lasted from June to August, with peaks around June and July. The monthly case reporting rate during the peak period ranged from 20.7% (4854/23,440) to 35% (12,135/34,706) of the total annual number of cases. Analysis of the pathogen composition of 2850 laboratory-confirmed cases identified 8 enterovirus serotypes, among which CV-A6 accounted for the highest proportion (652/2850, 22.88%). CV-A6 emerged as the major pathogen for HFMD in 2022 (203/732, 27.73%) and 2023 (262/708, 37.01%). We analyzed all CV-A6 full-length sequences in the NCBI database and the evolutionary features of viruses isolated in Henan. In China, the D3 subtype gradually appeared from 2011, and by 2019, all CV-A6 virus strains belonged to the D3 subtype. The VP1 sequences analyzed in Henan showed that its subtypes were consistent with the national subtypes. Furthermore, we analyzed the molecular evolutionary features of CV-A6 using Bayesian phylogeny and found that the most recent common ancestor of CV-A6 D3 dates back to 2006 in China, earlier than the 2011 HFMD outbreak. Moreover, the strains isolated in 2023 had mutations at several amino acid sites compared to the original strain. Conclusions The CV-A6 virus may have been introduced and circulating covertly within China prior to the large-scale HFMD outbreak. Our laboratory testing data confirmed the fluctuation and periodic patterns of CV-A6 prevalence. Our study provides valuable insights into understanding the evolutionary dynamics of CV-A6.
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