Abstract

BackgroundHuman bocavirus is a newly discovered parvovirus. Multiple studies have confirmed the presence of human bocavirus1 (HBoV1) in respiratory tract samples of children. The viral load, presentation of single detection and its role as a causative agent of severe respiratory tract infections have not been thoroughly elucidated.MethodsWe investigated the presence of HBoV1 by quantitative polymerase chain reaction (PCR) of nasopharyngeal aspirate specimens from 1229 children hospitalized for respiratory tract infections. The samples were analyzed for 15 respiratory viruses by PCR and 7 respiratory viruses by viral culture.ResultsAt least one virus was detected in 652 (53.1%) of 1229 children, and two or more viruses were detected in 266 (21.6%) children. HBoV1 was detected in 127 children (10.3%), in which 66/127 (52%) of the cases were the only HBoV1 virus detected. Seasonal variation was observed with a high HBoV1 infection rate in summer. A cutoff value of 107 copies/mL was used to distinguish high and low HBoV1 viral loads in the nasopharyngeal aspirates. High viral loads of HBoV1 were noted predominantly in the absence of other viral agents (28/39, 71.8%) whereas there was primarily co-detection in cases of low HBoV1 viral loads (50/88, 56.8%). There were no differences in the clinical symptoms and severity between HBoV1 single detection and co-detection. In cases of HBoV1 single detection, the high viral load group was more prevalent among children with dyspnea and wheezing than was the low viral load group (42.9% vs. 23.7%, P = 0.036; 60.7% vs. 31.6%, P = 0.018). In clinical severity, a significant difference was recorded (25.0% vs. 5.3%, P = 0.003) between high viral load and low viral load groups. Of the HBoV1 positive patients associated with severe respiratory tract infections, 10/18 (55.6%) patients belonged to the HBoV1 high viral load group, and 7/10 (70%) patients had cases of HBoV1 single detection.ConclusionsHBoV1 at a high viral load is not frequently found in co-detection with other respiratory viruses, and a single detection with a high viral load could be an etiological agent of severe respiratory tract infections.Electronic supplementary materialThe online version of this article (doi:10.1186/1471-2334-14-424) contains supplementary material, which is available to authorized users.

Highlights

  • Human bocavirus is a newly discovered parvovirus

  • Recent results obtained by quantitative realtime polymerase chain reaction (PCR) suggest that high Human bocavirus (HBoV) viral loads are frequently present as the sole viral finding for children admitted for respiratory tract infections (RTI) [4,5,8]

  • We investigated whether human bocavirus1 (HBoV1) at a high viral load increases the severity of RTI and whether co-detection with HBoV1 and another respiratory virus or viruses increases the severity of concurrent viral detection

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Summary

Introduction

Multiple studies have confirmed the presence of human bocavirus (HBoV1) in respiratory tract samples of children. The viral load, presentation of single detection and its role as a causative agent of severe respiratory tract infections have not been thoroughly elucidated. Human bocavirus (HBoV) was first described in 2005 in nasopharyngeal aspirates (NPAs) of children with respiratory tract infections (RTI). Jacques reported that HBoV at a high viral load could be an etiological agent of respiratory tract disease [4]. Recent results obtained by quantitative realtime PCR suggest that high HBoV viral loads (defined as > 106copies/mL) are frequently present as the sole viral finding for children admitted for RTI [4,5,8]. The role of HBoV as a causative agent in severe respiratory tract infections (SRTI) is unclear

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