Human Polyomavirus 6 Detected in Cases of Eosinophilic Pustular Folliculitis.


Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
28 05 2021
Historique:
received: 28 06 2020
accepted: 24 09 2020
pubmed: 30 9 2020
medline: 12 2 2022
entrez: 29 9 2020
Statut: ppublish

Résumé

Human polyomaviruses (HPyVs) have been associated with several cutaneous inflammatory conditions. More investigation is needed to identify further presentations of cutaneous pathology associated with HPyVs. Our aim was to investigate the possible association of skin-tropic HPyVs with folliculitis, particularly eosinophilic pustular folliculitis (EPF). This study included 55 Japanese patients, comprising 13 patients with EPF and 42 patients with suppurative folliculitis. HPyV DNAs were detected by quantitative polymerase chain reaction. Expression of viral antigen and geographically related viral genotypes were also assessed. Human polyomavirus 6 (HPyV6) DNA was found in 9 of 13 (69%) patients with EPF, a rate significantly higher than that found in suppurative folliculitis (1/42; 2%). Of the 7 HPyV6 DNA-positive EPF specimens analyzed, 4 were positive for HPyV6 small tumor antigen. All the HPyV6 strains detected in this study were of the Asian/Japanese genotype. The predominant detection of HPyV6 DNA and the expression of viral antigen suggest a possible association between HPyV6 infection and EPF in a subset of patients. Worldwide studies are warranted to determine whether Asian/Japanese genotype HPyV6 is associated preferentially with the incidence and pathogenesis of this eosinophil-related skin disease that has an ethnic predilection for the East Asian population.

Sections du résumé

BACKGROUND
Human polyomaviruses (HPyVs) have been associated with several cutaneous inflammatory conditions. More investigation is needed to identify further presentations of cutaneous pathology associated with HPyVs. Our aim was to investigate the possible association of skin-tropic HPyVs with folliculitis, particularly eosinophilic pustular folliculitis (EPF).
METHODS
This study included 55 Japanese patients, comprising 13 patients with EPF and 42 patients with suppurative folliculitis. HPyV DNAs were detected by quantitative polymerase chain reaction. Expression of viral antigen and geographically related viral genotypes were also assessed.
RESULTS
Human polyomavirus 6 (HPyV6) DNA was found in 9 of 13 (69%) patients with EPF, a rate significantly higher than that found in suppurative folliculitis (1/42; 2%). Of the 7 HPyV6 DNA-positive EPF specimens analyzed, 4 were positive for HPyV6 small tumor antigen. All the HPyV6 strains detected in this study were of the Asian/Japanese genotype.
CONCLUSIONS
The predominant detection of HPyV6 DNA and the expression of viral antigen suggest a possible association between HPyV6 infection and EPF in a subset of patients. Worldwide studies are warranted to determine whether Asian/Japanese genotype HPyV6 is associated preferentially with the incidence and pathogenesis of this eosinophil-related skin disease that has an ethnic predilection for the East Asian population.

Identifiants

pubmed: 32989462
pii: 5912687
doi: 10.1093/infdis/jiaa607
doi:

Substances chimiques

Antigens, Viral 0
DNA, Viral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1724-1732

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Yumiko Hashida (Y)

Department of Microbiology and Infection, Kochi Medical School, Kochi University, Kochi, Japan.

Tomonori Higuchi (T)

Department of Microbiology and Infection, Kochi Medical School, Kochi University, Kochi, Japan.

Saeko Nakajima (S)

Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Kimiko Nakajima (K)

Department of Dermatology, Kochi Medical School, Kochi University, Kochi, Japan.

Takako Ujihara (T)

Department of Microbiology and Infection, Kochi Medical School, Kochi University, Kochi, Japan.
Science Research Center, Kochi Medical School, Kochi University, Kochi, Japan.

Kenji Kabashima (K)

Department of Dermatology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Singapore Immunology Network and Skin Research Institute of Singapore, Agency for Science, Technology and Research, Singapore.

Shigetoshi Sano (S)

Department of Dermatology, Kochi Medical School, Kochi University, Kochi, Japan.

Masanori Daibata (M)

Department of Microbiology and Infection, Kochi Medical School, Kochi University, Kochi, Japan.

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Classifications MeSH