Recombination analysis of intermediate human adenovirus type 53 in Japan by complete genome sequence

Author:

Kaneko Hisatoshi1,Aoki Koki2,Ishida Susumu2,Ohno Shigeaki3,Kitaichi Nobuyoshi43,Ishiko Hiroaki5,Fujimoto Tsuguto6,Ikeda Yoshifumi7,Nakamura Masako8,Gonzalez Gabriel9,Koyanagi Kanako O.9,Watanabe Hidemi9,Suzutani Tatsuo1

Affiliation:

1. Department of Microbiology, Fukushima Medical University School of Medicine, Fukushima, Japan

2. Department of Ophthalmology, Hokkaido University Graduate School of Medicine, Sapporo, Japan

3. Department of Ocular Inflammation and Immunology, Hokkaido University Graduate School of Medicine, Sapporo, Japan

4. Department of Ophthalmology, Health Sciences University of Hokkaido, Sapporo, Japan

5. Host Defense Laboratory, Mitsubishi Chemical Medience Corporation, Tokyo, Japan

6. National Institute of Infectious Diseases, Tokyo, Japan

7. Hiroshima City Institute of Public Health, Hiroshima, Japan

8. Fukui Prefectural Institute of Public Health and Environmental Science, Fukui, Japan

9. Laboratory of Genome Sciences, Research Groups of Bioinformatics, Division of Bioengineering and Bioinformatics, Hokkaido University Graduate School of Information Science and Technology, Sapporo, Japan

Abstract

Human adenovirus type 53 (HAdV-53) has commonly been detected in samples from epidemic keratoconjunctivitis (EKC) patients in Japan since 1996. HAdV-53 is an intermediate virus, containing hexon-chimeric, penton base and fiber structures similar to HAdV-22 and -37, HAdV-37 and HAdV-8, respectively. HAdV-53-like intermediate strains were first isolated from EKC samples in Japan in the 1980s. Here, the complete genome sequences of three such HAdV-53-like intermediate strains (870006C, 880249C and 890357C) and four HAdV-53 strains were determined, and their relationships were analysed. The seven HAdV strains were classified into three groups, 870006C/880249C, 890357C and the four HAdV-53 strains, on the basis of phylogenetic analyses of the partial and complete genome sequences. HAdV strains within the same group showed the highest nucleotide identities (99.87–100.00 %). Like HAdV-53, the hexon loop 1 and 2 regions of 870006C, 880249C and 890357C showed the highest identity with HAdV-22. However, these strains did not show a hexon-chimeric structure similar to HAdV-22 and -37, or a penton base similar to HAdV-37. The fiber genes of 870006C and 880249C were identical to that of HAdV-37, but not HAdV-8. Thus, the three intermediate HAdVs isolated in the 1980s were similar to each other but not to HAdV-53. The recombination breakpoints were inferred by the Recombination Detection Program (rdp) using whole-genome sequences of these seven HAdV and of 12 HAdV-D strains from GenBank. HAdV-53 may have evolved from intermediate HAdVs circulating in the 1980s, and from HAdV-8, -22 and -37, by recombination of sections cut at the putative breakpoints.

Publisher

Microbiology Society

Subject

Virology

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