Suppiah Jeyanthi, Zulkifli Murni Maya Sari, Adiee Amir Hussin, Zainudin Nur Ain Zahidah, Dukut Soeharto Mazrul Effendy, Ramli Nuraisyah, Wan Ming Keong, Sulong Mohd Rahim, Suli Zailiza, Mohd Zain Rozainanee
Virology Unit, Infectious Disease Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health, Shah Alam, Selangor, Malaysia.
Vector-Borne Disease Sector, Disease Control Division, Ministry of Health, Putrajaya, Malaysia.
Trop Med Health. 2025 Aug 25;53(1):114. doi: 10.1186/s41182-025-00795-5.
Sylvatic dengue viruses, typically maintained in non-human primate and forest mosquito cycles, have rarely been associated with human infections. However, sporadic spillovers have been reported in Southeast Asia, including Malaysia. These events are often under-detected due to the genetic divergence of sylvatic strains from endemic urban dengue viruses. During routine surveillance in Malaysia (2024-2025), a subset of clinically confirmed dengue cases yielded undetectable serotype results by commercial real-time reverse transcription polymerase chain reaction (RT-PCR) assays, prompting investigation into a possible sylvatic origin.
We investigated 22 such cases through clinical, serological, molecular, and phylogenetic analyses. NS1 antigen and broad-range RT-PCR confirmed acute dengue infection. Selected samples underwent sequencing and lineage determination.
Most patients presented with severe dengue during early illness (mean day 3), with 95.5% NS1 positivity and predominantly primary infection profiles. Despite serotyping failure, sequencing revealed that eight of nine analyzed samples belonged to sylvatic DENV2, while one represented a divergent DENV3. Comparative amino acid analysis uncovered a unique signature in recent Malaysian sylvatic DENV2 strains, differentiating them from both urban and historical sylvatic lineages. This includes the V270 mutation in the M gene; R844, V884, and I898 in the NS1 gene; T1207 in the NS2A gene; A1597 in the NS3 gene; and D3048 and I3373 in the NS5 gene. Phylogenetic analysis clustered these strains into a distinct Malaysian clade, separate from the African sylvatic lineage.
This study provides the first genomic evidence of a recent sylvatic DENV2 spillover into humans in Malaysia, likely undetected by standard diagnostics due to genetic divergence. These findings underscore the urgent need to enhance surveillance tools and explore the sylvatic transmission cycle's role in dengue epidemiology.
丛林型登革病毒通常在非人灵长类动物和森林蚊子的循环中维持传播,很少与人类感染相关。然而,在东南亚地区,包括马来西亚,已有零星的病毒外溢事件报道。由于丛林型毒株与地方性城市登革病毒存在基因差异,这些事件往往未被充分检测到。在马来西亚的常规监测(2024 - 2025年)期间,一部分临床确诊的登革热病例通过商业实时逆转录聚合酶链反应(RT-PCR)检测未得出血清型结果,这促使人们对可能的丛林型病毒起源展开调查。
我们通过临床、血清学、分子和系统发育分析对22例此类病例进行了调查。NS1抗原检测和广谱RT-PCR证实为急性登革热感染。选取的样本进行了测序和谱系确定。
大多数患者在疾病早期(平均第3天)表现为重症登革热,NS1阳性率为95.5%,且主要为初次感染特征。尽管血清分型失败,但测序显示,9个分析样本中有8个属于丛林型登革病毒2型(DENV2),1个代表一种不同的登革病毒3型(DENV3)。氨基酸比较分析发现,近期马来西亚丛林型DENV2毒株具有独特的特征,使其与城市和历史丛林型谱系区分开来。这包括M基因中的V270突变;NS1基因中的R844、V884和I898;NS2A基因中的T1207;NS3基因中的A1597;以及NS5基因中的D3048和I3373。系统发育分析将这些毒株聚类为一个独特的马来西亚分支,与非洲丛林型谱系不同。
本研究提供首个基因组证据,证明近期马来西亚存在丛林型DENV2病毒外溢感染人类的情况,由于基因差异,标准诊断方法可能未检测到。这些发现强调迫切需要加强监测工具,并探索丛林型传播循环在登革热流行病学中的作用。