Polyomaviruses-associated respiratory infections in HIV-infected and HIV-uninfected children

被引:6
|
作者
Nunes, Marta C. [1 ,2 ]
Kuschner, Zachary [3 ]
Rabede, Zelda [2 ]
Cutland, Clare L. [1 ,2 ]
Madimabe, Richard [1 ,2 ]
Kuwanda, Locadiah [1 ,2 ]
Klugman, Keith P. [2 ,4 ,5 ]
Adrian, Peter V. [1 ,2 ]
Madhi, Shabir A. [1 ,2 ,6 ]
机构
[1] Univ Witwatersrand, Natl Res Fdn Vaccine Preventable Dis, Dept Sci & Technol, Johannesburg, South Africa
[2] Univ Witwatersrand, Fac Hlth Sci, MRC, Resp & Meningeal Pathogens Res Unit, Johannesburg, South Africa
[3] SUNY Stony Brook, Stony Brook Sch Med, Stony Brook, NY 11794 USA
[4] Emory Univ, Sch Med, Rollins Sch Publ Hlth, Hubert Dept Global Hlth, Atlanta, GA USA
[5] Emory Univ, Sch Med, Div Infect Dis, Atlanta, GA USA
[6] Ctr Vaccines & Immunol, Natl Inst Communicable Dis, Johannesburg, South Africa
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
Polyomaviruses; HIV; Pneumonia; Respiratory infections; PCV9; Pneumococcal vaccine; IMMUNODEFICIENT CHILD; TRACT INFECTIONS; KI; WU; PNEUMONIA; DISEASE; VIRUS; CONJUGATE; BURDEN; TRIAL;
D O I
10.1016/j.jcv.2014.10.013
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Two recently discovered polyomaviruses (PyV), WU and KI, have been identified in respiratory-tract specimens from children with acute respiratory infections, although there are limited data in HIV-infected children. Objectives: To determine the prevalence and clinical manifestations of WUPyV and KIPyV-associated lower respiratory tract infections (LRTIs) hospitalization in HIV-infected and -uninfected children; and probe the role of pneumococcal co-infection. Study design: Nasopharyngeal aspirates were collected from a cohort of 39,836 children randomized to receive 9-valent pneumococcal conjugate vaccine (PCV9) or placebo when hospitalized for LRTIs, and were screened by PCR for WUPyV, KIPyV and other respiratory viruses. Results: In placebo-recipients the prevalence of WUPyV was 6.3% (18/285) in HIV-infected and 13.9% (66/476) in HIV-uninfected children (p = 0.002). In WUPyV-positive LRTIs HIV-infected children had lower oxygen saturation at admission and a higher case fatality rate (11.1% vs. 0%; p = 0.04). KIPyV was identified in 10.2% (29/285) of HIV-infected and in 7.4% (35/476) of HIV-uninfected placebo-recipients with LRTIs (p = 0.13). HIV-infected compared to HIV-uninfected children with KIPyV-positive LRTIs had lower oxygen saturation, higher respiratory rate and longer duration of hospitalization. Co-infections with other respiratory-viruses were detected in 65.5% of WUPyV-positive LRTIs and in 75.0% of KIPyV-positive LRTIs. Among HIV-uninfected children, there was a lower incidence of hospitalization for clinical pneumonia episodes in which KIPyV (80%; 95% CI: 41,93) and WUPyV (49%; 95% CI: 9, 71) were identified among PCV9-recipients compared to placebo-recipients. Conclusions: Polyomaviruses were commonly identified in HIV-infected and -uninfected children hospitalized for LRTIs, frequently in association with other viruses and may contribute to the pathogenesis of pneumococcal pneumonia. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:571 / 578
页数:8
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