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1978 年至 2006 年中国南方登革热病毒的分子流行病学研究。

Molecular epidemiology of dengue viruses in southern China from 1978 to 2006.

机构信息

Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing 100029, China.

出版信息

Virol J. 2011 Jun 26;8:322. doi: 10.1186/1743-422X-8-322.

Abstract

To investigate molecular epidemiology of dengue viruses (DENV) in southern China, a total of 14 dengue isolates were collected in southern China during each epidemic year between 1978 and 2006 and their full-length genome sequences were obtained by using RT-PCR method. The E gene sequences from additional 6 dengue fever patients in Guangzhou in 2006 were also obtained by using RT-PCR method. Combined with DENVs sequences published in GenBank, phylogenetic analysis and recombination analysis were performed. One hundred and twenty-five E gene sequences and 60 complete genome sequences published in the GenBank were also involved. Phylogenetic analysis showed that there was a wide genetic diversity of DENVs isolated in southern China. DENV-1 strains exist in almost all of the clades of genotype I and IV except the Asia 1 clade of genotype I; DENV-2 stains are grouped into four of the five genotypes except American genotype. DENV-4 strains are grouped into 2 genotypes (I and II). Phylogenetic analysis also showed that all DENV-4 isolates and two DENV-2 isolates were closely related to the prior isolates from neighboring Southeast Asia countries. The DENV-1 strain isolated during the 2006 epidemic is highly homologous to the strains isolated during the 2001 epidemic.Recombination analysis showed no inter-serotype recombination, but 22 intra-serotype recombination events were found across the 32 complete genomes of all Chinese isolates. The study suggested that dengue fever epidemic in Southern China over the past 30 years presented two important modes, 1) imported-cases-induced endemic prevalence; 2) endogenous epidemic outbreak with natural epidemic focus. Recombination may play an important role in dengue virus evolution and adaptation.

摘要

为了调查中国南方登革热病毒(DENV)的分子流行病学,我们在 1978 年至 2006 年期间每个流行年份共收集了 14 株登革热分离株,并通过 RT-PCR 方法获得了它们的全长基因组序列。我们还通过 RT-PCR 方法获得了来自广州的 6 例 2006 年登革热患者的 E 基因序列。结合 GenBank 中发布的 DENVs 序列,进行了系统发育分析和重组分析。还涉及了 125 个 E 基因序列和 60 个完整基因组序列。系统发育分析表明,中国南方分离的 DENVs 存在广泛的遗传多样性。DENV-1 株存在于几乎所有的 I 型和 IV 型基因型的分支中,除了 I 型的亚洲 1 分支;DENV-2 株分为除了美洲基因型外的五个基因型中的四个。DENV-4 株分为 2 个基因型(I 和 II)。系统发育分析还表明,所有 DENV-4 分离株和 2 株 DENV-2 分离株与来自邻近东南亚国家的先前分离株密切相关。2006 年流行期间分离的 DENV-1 株与 2001 年流行期间分离的株高度同源。重组分析表明没有血清型间重组,但在所有中国分离株的 32 个完整基因组中发现了 22 个血清型内重组事件。该研究表明,过去 30 年中国南方的登革热流行呈现出两种重要模式,1)输入性病例引起的地方性流行;2)以自然流行疫区为中心的内源性流行爆发。重组可能在登革热病毒的进化和适应中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b264/3138434/14165566d36c/1743-422X-8-322-2.jpg

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