Evidence of the simultaneous replications of active viruses in specimens positive for multiple respiratory viruses

Author:

Kawase Miyuki1,Suwa Reiko1,Sugimoto Satoko1,Kakizaki Masatoshi1,Kume Yohei2,Chishiki Mina2,Ono Takashi2,Okabe Hisao2,Norito Sakurako2,Ujike Makoto3ORCID,Hosoya Mitsuaki2,Hashimoto Koichi2ORCID,Shirato Kazuya1ORCID

Affiliation:

1. Department of Virology III, National Institute of Infectious Disease , Gakuen, Musashimurayama, Tokyo, Japan

2. Department of Pediatrics, School of Medicine, Fukushima Medical University , Hikarigaoka, Fukushima, Japan

3. Faculty of Veterinary Medicine, Nippon Veterinary and Life Science University , Musashino, Tokyo, Japan

Abstract

ABSTRACT Genetic diagnostic assays for the detection of respiratory viruses sometimes show simultaneous multiple infections with low copy numbers. In such cases, the disease is considered caused by a single etiologic agent and others are nonspecific reactions and/or contaminations. Interferon-dependent interference is seen in dual infections of influenza and respiratory syncytial virus, which are the main causes of respiratory infections. Virus isolation is one of the answers in detecting other active viruses present in specimens, and the air–liquid interface culture of human bronchial/tracheal epithelial cells (HBTEC-ALI) is optimal for the isolation of respiratory viruses owing to its wide range of susceptibility. In this study, we successfully confirmed the replications of various viruses from specimens with low copy numbers and simultaneous passage of two to three viruses using HBTEC-ALI cultures, mainly including human bocavirus 1 and/or human rhinovirus. IMPORTANCE Since the pandemic of coronavirus diseases 2019, the use of real-time PCR assay has become widespread among people who were not familiar with it in virus detection. As a result, whether a high real-time PCR value in one time test indicates virus transmissibly became a complicated social problem, regardless of the difference in assays and/or amplification conditions, the time and number of diagnostic test during the time course of infection. In addition, the multiple positives in the test of respiratory viruses further add to the confusion in the interpretation of the infection. To address this issue, we performed virus isolation using pediatric SARI (severe acute respiratory infections) specimens on air–liquid interface culture of human bronchial/tracheal epithelial cell culture. The result of this study can be a strong evidence that the specimens showing positivity for multiple agents in real-time PCR tests possibly contain infectious viruses.

Funder

Japan Agency for Medical Research and Development

MEXT | Japan Society for the Promotion of Science

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Cell Biology,Microbiology (medical),Genetics,General Immunology and Microbiology,Ecology,Physiology

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