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An Efficient Method for Adenovirus Production
Published on: June 10, 2021
Description of an adenovirus A31 outbreak in a paediatric haematology unit
M Leruez-Ville1, M Chardin-Ouachée, B Neven
1Laboratoire de Virologie, EA 3620 Université Paris V, Hôpital Necker-Enfants Malades AP-HP, Paris, France. marianne.leruez@nck.ap-hop-paris.fr
Insights
Adenovirus A31 caused an epidemic in pediatric stem cell transplant patients. This study highlights the need to assess the burden of this specific adenovirus genotype in this vulnerable population.
Area of Science:
- Virology
- Pediatric Hematology
- Infectious Diseases
Background:
- Allogeneic haematopoietic stem cell transplantation (hSCT) in children carries a high risk of adenovirus infections, leading to significant morbidity and mortality.
- While species C and B adenoviruses are most common post-hSCT, adenovirus A31 has emerged as a growing concern.
Purpose of the Study:
- To investigate an outbreak of adenovirus A31 infections in pediatric hSCT patients.
- To characterize the clinical features and epidemiological spread of adenovirus A31 genotype.
Main Methods:
- Quantitative real-time PCR was used to screen blood samples from 58 hSCT children for adenovirus species A-C over three years.
- Phylogenetic analysis, including hexon gene amplification and sequencing, was performed on detected adenovirus strains.
Main Results:
- Fifteen cases of adenovirus viraemia were identified in the study period.
- Seven cases occurring in spring/summer 2003 were identified as adenovirus species A, specifically genotype A31, with 100% hexon gene homology.
- Clinical data for these seven patients with A31 adenovirus viraemia were documented.
Conclusions:
- An epidemic spread of adenovirus genotype A31 was observed in a pediatric hematology unit.
- Epidemiological data strongly suggest a nosocomial (hospital-acquired) origin for this A31 adenovirus outbreak.
- Further assessment of the burden of adenovirus A31 infection in hSCT recipients is warranted.
Abstract:
Adenovirus infections result in significant morbidity and mortality in allogeneic haematopoietic stem cell transplanted (hSCT) children. Adenovirus from species C and B account for more than 90% of adenoviruses recovered after hSCT. However, infections due to adenovirus A31 have been increasingly reported in recent years. Between April 2002 and April 2005, blood samples obtained every 2 weeks from 58 hSCT children were screened for adenovirus species A to C by quantitative real-time PCR. Phylogenetic analysis was realized after amplification and sequencing of the entire hexon gene. Fifteen cases of adenovirus infection with viraemia were recovered during this 3 years period. During spring/summer 2003, seven cases occurred and were due to an adenovirus species A. Phylogenetic analysis of the seven strains showed that they belonged to the A31 genotype and shared 100% homology. Clinical features of the seven HSCT children with A31 adenovirus viraemia are described. We describe here an epidemic spread of adenovirus genotype A31 in a paediatric haematology unit. Timing, location and hexon gene genotyping results highly suggested a nosocomial origin to this epidemic. The burden of adenovirus A31 infection needs to be further assessed in this context.
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