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Human Bocavirus 1 Primary Infection and Shedding in Infants
Emily T Martin1, Jane Kuypers2, John P McRoberts3
1University of Michigan, Ann Arbor.
Insights
Human bocavirus 1 (HBoV-1) primary infections are linked to mild respiratory illness in children. Subsequent prolonged HBoV-1 DNA detection and reinfection contribute to long-term shedding.
Area of Science:
- Pediatric infectious diseases
- Virology
- Respiratory illnesses
Background:
- Human bocavirus 1 (HBoV-1) is frequently detected in young children.
- The precise role of HBoV-1 in pediatric respiratory illness remains unclear due to its common detection in asymptomatic individuals.
Purpose of the Study:
- To investigate the association between HBoV-1 primary shedding events and respiratory symptoms in infants.
- To determine the duration and patterns of HBoV-1 shedding and reinfection in a longitudinal cohort.
Main Methods:
- Quantitative polymerase chain reaction (qPCR) was used to test weekly oral fluid samples from infants for HBoV-1 DNA.
- Symptoms during HBoV-1 primary shedding were compared to control periods.
- Single-nucleotide polymorphisms were analyzed to identify HBoV-1 variants.
Main Results:
- 76% of infants (66/87) experienced primary HBoV-1 infection.
- HBoV-1 DNA was detected for over a month in 42/66 primary shedding events.
- Children were more likely to have new cough symptoms (OR 2.7) and seek healthcare (OR 2.8) during initial HBoV-1 detection.
Conclusions:
- Primary HBoV-1 shedding events correlate with mild respiratory illness.
- Prolonged HBoV-1 DNA detection, lasting up to a year, is observed post-primary infection.
- HBoV-1 reinfection plays a role in the extended shedding patterns.
Background:
Human bocavirus 1 (HBoV-1) is frequently detected in young children. The role of HBoV-1 in respiratory illness is unclear, owing to frequent detection in asymptomatic children.
Methods:
Weekly oral fluid samples from a longitudinal cohort of infants were tested by quantitative polymerase chain reaction for HBoV-1 DNA. Symptoms during HBoV-1 primary shedding events were compared to those during 14-day control periods occurring 1 month prior to and following the primary event. Eight single-nucleotide polymorphisms were analyzed to assess HBoV-1 variants.
Results:
Sixty-six of 87 children (76%), followed for at least 18 months from birth, had a primary HBoV-1 infection. HBoV-1 was consistently detected for >1 month (maximum duration, 402 days) following 42 of 66 primary shedding events. Children were more likely to experience new cough symptoms (odds ratio [OR], 2.7; 95% confidence interval [CI], 1.4-5.5) and to visit a healthcare provider (OR, 2.8; 95% CI, 1.02-7.7) during the 14 days surrounding the time of initial detection of HBoV-1. Recurrent HBoV-1 shedding events were found in 33 children (50%). Twelve of 48 children with HBoV-1 variant data had multiple viral allelic patterns over time.
Conclusions:
HBoV-1 primary shedding events are associated with mild respiratory illness with subsequent prolonged detection of HBoV-1 DNA for up to a year. HBoV-1 reinfection contributes to long-term shedding.
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