Faculdade de Medicina de São José do Rio Preto, São José do Rio Preto, Brazil.
PLoS Negl Trop Dis. 2009 May 26;3(5):e448. doi: 10.1371/journal.pntd.0000448.
The dengue virus has a single-stranded positive-sense RNA genome of approximately 10.700 nucleotides with a single open reading frame that encodes three structural (C, prM, and E) and seven nonstructural (NS1, NS2A, NS2B, NS3, NS4A, NS4B, and NS5) proteins. It possesses four antigenically distinct serotypes (DENV 1-4). Many phylogenetic studies address particularities of the different serotypes using convenience samples that are not conducive to a spatio-temporal analysis in a single urban setting. We describe the pattern of spread of distinct lineages of DENV-3 circulating in São José do Rio Preto, Brazil, during 2006. Blood samples from patients presenting dengue-like symptoms were collected for DENV testing. We performed M-N-PCR using primers based on NS5 for virus detection and identification. The fragments were purified from PCR mixtures and sequenced. The positive dengue cases were geo-coded. To type the sequenced samples, 52 reference sequences were aligned. The dataset generated was used for iterative phylogenetic reconstruction with the maximum likelihood criterion. The best demographic model, the rate of growth, rate of evolutionary change, and Time to Most Recent Common Ancestor (TMRCA) were estimated. The basic reproductive rate during the epidemics was estimated. We obtained sequences from 82 patients among 174 blood samples. We were able to geo-code 46 sequences. The alignment generated a 399-nucleotide-long dataset with 134 taxa. The phylogenetic analysis indicated that all samples were of DENV-3 and related to strains circulating on the isle of Martinique in 2000-2001. Sixty DENV-3 from São José do Rio Preto formed a monophyletic group (lineage 1), closely related to the remaining 22 isolates (lineage 2). We assumed that these lineages appeared before 2006 in different occasions. By transforming the inferred exponential growth rates into the basic reproductive rate, we obtained values for lineage 1 of R(0) = 1.53 and values for lineage 2 of R(0) = 1.13. Under the exponential model, TMRCA of lineage 1 dated 1 year and lineage 2 dated 3.4 years before the last sampling. The possibility of inferring the spatio-temporal dynamics from genetic data has been generally little explored, and it may shed light on DENV circulation. The use of both geographic and temporally structured phylogenetic data provided a detailed view on the spread of at least two dengue viral strains in a populated urban area.
登革热病毒是一种单链正链 RNA 基因组,约有 10700 个核苷酸,具有一个单一的开放阅读框,编码三个结构蛋白(C、prM 和 E)和七个非结构蛋白(NS1、NS2A、NS2B、NS3、NS4A、NS4B 和 NS5)。它有四个具有不同抗原性的血清型(DENV1-4)。许多系统发育研究使用非便利样本来研究不同血清型的特殊性,而这些样本不利于在单一城市环境中进行时空分析。我们描述了 2006 年巴西圣若泽-杜里奥普雷托(São José do Rio Preto)循环的不同血清型 3 型登革热病毒(DENV-3)的传播模式。采集有登革热样症状的患者的血液样本进行登革热检测。我们使用基于 NS5 的引物进行 M-N-PCR 以检测和鉴定病毒。从 PCR 混合物中纯化片段并进行测序。对阳性登革热病例进行地理编码。为了对测序样本进行分型,我们对 52 个参考序列进行了比对。生成的数据集用于使用最大似然准则进行迭代系统发育重建。估计了最佳人口统计模型、增长率、进化变化率和最近共同祖先的时间(TMRCA)。估计了流行期间的基本繁殖率。我们从 174 份血样中的 82 名患者中获得了序列。我们能够对 46 个序列进行地理编码。比对生成了一个 399 个核苷酸长的数据集,包含 134 个分类单元。系统发育分析表明,所有样本均为 DENV-3,与 2000-2001 年马提尼克岛流行的菌株有关。来自圣若泽-杜里奥普雷托的 60 株 DENV-3 形成一个单系群(谱系 1),与其余 22 株(谱系 2)密切相关。我们假设这些谱系在不同时间出现在 2006 年之前。通过将推断的指数增长率转换为基本繁殖率,我们得到了谱系 1 的 R(0) = 1.53 和谱系 2 的 R(0) = 1.13 的值。在指数模型下,谱系 1 的 TMRCA 为最后一次采样前 1 年,谱系 2 的 TMRCA 为 3.4 年。从遗传数据推断时空动态的可能性尚未得到广泛探索,它可能为登革热病毒的传播提供新的见解。使用地理和时间结构的系统发育数据提供了一个详细的视图,了解至少两种登革热病毒株在人口稠密的城市地区的传播情况。