Human parvovirus B19 infection in dengue patients and potential association with disease progression and clinical outcomes

登革热患者中人细小病毒B19感染及其与疾病进展和临床结局的潜在关联

阅读:1

Abstract

OBJECTIVES: Many viruses can present with clinical symptoms resembling dengue fever (DF), including human parvovirus B19 (B19V). Therefore, patients with DF are not often tested for secondary pathogens. The current study aimed to investigate B19V infection and its association with clinical features in dengue patients. METHODS: A total of 230 subjects were recruited for this study, including patients with DF (n = 86), DF with warning signs (DWS, n = 53), and healthy controls (n = 91). Plasma samples were analyzed for B19V using enzyme-linked immunosorbent assay, nested polymerase chain reaction, sequencing, and phylogenetic analysis. The potential association between B19V infection and dengue progression was investigated. RESULTS: Anti-B19V immunoglobulin M antibodies were detected across all groups: 17.4% in the DF group, 7.5% in the DWS group, and 13.2% in healthy controls. Anti-B19V immunoglobulin G positivity was most prevalent in DF patients (26.7%), followed by healthy controls (22.0%) and DWS patients (20.8%). B19V DNA was identified in 10 of 139 dengue patients (7.2%), but not in healthy controls. The rate of B19V infection was significantly higher in DWS patients than in those with DF, suggesting that B19V infection during dengue may be associated with an increased risk of a more severe form of disease (odds ratio = 4.4, P = 0.043). B19V-positive dengue patients had lower platelet counts compared with B19V-negative patients (P = 0.046), although multivariate analysis revealed no significant difference. In addition, only genotype 1, specifically subgenotype 1A, was detected. CONCLUSIONS: This study reports the prevalence of B19V infection in Vietnamese dengue patients and reveals a potential association with dengue progression and clinical features.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。