Transmission of Rat Hepatitis E Virus Infection to Humans in Hong Kong: A Clinical and Epidemiological Analysis.


Journal

Hepatology (Baltimore, Md.)
ISSN: 1527-3350
Titre abrégé: Hepatology
Pays: United States
ID NLM: 8302946

Informations de publication

Date de publication:
01 2021
Historique:
received: 15 10 2019
accepted: 23 12 2019
pubmed: 22 1 2020
medline: 22 6 2021
entrez: 22 1 2020
Statut: ppublish

Résumé

Hepatitis E virus (HEV) variants causing human infection predominantly belong to HEV species A (HEV-A). HEV species C genotype 1 (HEV-C1) circulates in rats and is highly divergent from HEV-A. It was previously considered unable to infect humans, but the first case of human HEV-C1 infection was recently discovered in Hong Kong. The aim of this study is to further describe the features of this zoonosis in Hong Kong. We conducted a territory-wide prospective screening study for HEV-C1 infection over a 31-month period. Blood samples from 2,860 patients with abnormal liver function (n = 2,201) or immunosuppressive conditions (n = 659) were screened for HEV-C1 RNA. In addition, 186 captured commensal rats were screened for HEV-C1 RNA. Sequences of human-derived and rat-derived HEV-C1 isolates were compared. Epidemiological and clinical features of HEV-C1 infection were analyzed. HEV-C1 RNA was detected in 6/2,201 (0.27%) patients with hepatitis and 1/659 (0.15%) immunocompromised persons. Including the previously reported case, eight HEV-C1 infections were identified, including five in patients who were immunosuppressed. Three patients had acute hepatitis, four had persistent hepatitis, and one had subclinical infection without hepatitis. One patient died of meningoencephalitis, and HEV-C1 was detected in cerebrospinal fluid. HEV-C1 hepatitis was generally milder than HEV-A hepatitis. HEV-C1 RNA was detected in 7/186 (3.76%) rats. One HEV-C1 isolate obtained from a rat captured near the residences of patients was closely related to the major outbreak strain. HEV-C1 is a cause of hepatitis E in humans in Hong Kong. Immunosuppressed individuals are susceptible to persistent HEV-C1 infection and extrahepatic manifestations. Subclinical HEV-C1 infection threatens blood safety. Tests for HEV-C1 are required in clinical laboratories.

Sections du résumé

BACKGROUND AND AIMS
Hepatitis E virus (HEV) variants causing human infection predominantly belong to HEV species A (HEV-A). HEV species C genotype 1 (HEV-C1) circulates in rats and is highly divergent from HEV-A. It was previously considered unable to infect humans, but the first case of human HEV-C1 infection was recently discovered in Hong Kong. The aim of this study is to further describe the features of this zoonosis in Hong Kong.
APPROACH AND RESULTS
We conducted a territory-wide prospective screening study for HEV-C1 infection over a 31-month period. Blood samples from 2,860 patients with abnormal liver function (n = 2,201) or immunosuppressive conditions (n = 659) were screened for HEV-C1 RNA. In addition, 186 captured commensal rats were screened for HEV-C1 RNA. Sequences of human-derived and rat-derived HEV-C1 isolates were compared. Epidemiological and clinical features of HEV-C1 infection were analyzed. HEV-C1 RNA was detected in 6/2,201 (0.27%) patients with hepatitis and 1/659 (0.15%) immunocompromised persons. Including the previously reported case, eight HEV-C1 infections were identified, including five in patients who were immunosuppressed. Three patients had acute hepatitis, four had persistent hepatitis, and one had subclinical infection without hepatitis. One patient died of meningoencephalitis, and HEV-C1 was detected in cerebrospinal fluid. HEV-C1 hepatitis was generally milder than HEV-A hepatitis. HEV-C1 RNA was detected in 7/186 (3.76%) rats. One HEV-C1 isolate obtained from a rat captured near the residences of patients was closely related to the major outbreak strain.
CONCLUSIONS
HEV-C1 is a cause of hepatitis E in humans in Hong Kong. Immunosuppressed individuals are susceptible to persistent HEV-C1 infection and extrahepatic manifestations. Subclinical HEV-C1 infection threatens blood safety. Tests for HEV-C1 are required in clinical laboratories.

Identifiants

pubmed: 31960460
doi: 10.1002/hep.31138
doi:

Substances chimiques

RNA, Viral 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

10-22

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© 2020 by the American Association for the Study of Liver Diseases.

Références

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Auteurs

Siddharth Sridhar (S)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong, Hong Kong, China.
Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, China.

Cyril Chik-Yan Yip (CC)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Shusheng Wu (S)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Nicholas Foo-Siong Chew (NF)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Kit-Hang Leung (KH)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Jasper Fuk-Woo Chan (JF)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong, Hong Kong, China.
Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, China.

Pyrear Suhui Zhao (PS)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Wan-Mui Chan (WM)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Rosana Wing-Shan Poon (RW)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Hoi-Wah Tsoi (HW)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Jian-Piao Cai (JP)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Helen Shuk-Ying Chan (HS)

The Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The University of Hong Kong, Hong Kong, China.

Anthony Wai-Shing Leung (AW)

Queen Elizabeth Hospital, Hong Kong, China.

Cindy Wing-Sze Tse (CW)

Princess Margaret Hospital, Hong Kong, China.

Jonpaul Sze-Tsing Zee (JS)

Kwong Wah Hospital, Hong Kong, China.

Owen Tak-Yin Tsang (OT)

Queen Elizabeth Hospital, Hong Kong, China.

Vincent Chi-Chung Cheng (VC)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.

Susanna Kar-Pui Lau (SK)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong, Hong Kong, China.
Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, China.
Tuen Mun Hospital, Hong Kong, China.

Patrick Chiu-Yat Woo (PC)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong, Hong Kong, China.
Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, China.
Tuen Mun Hospital, Hong Kong, China.

Dominic Ngai-Chong Tsang (DN)

Department of Health, Public Health Laboratory Services Branch, Hong Kong, China.

Kwok-Yung Yuen (KY)

Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Emerging Infectious Diseases, The University of Hong Kong, Hong Kong, China.
Carol Yu Centre for Infection, The University of Hong Kong, Hong Kong, China.
Tuen Mun Hospital, Hong Kong, China.

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