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Article: Transmission of rat hepatitis E virus infection to humans in Hong Kong: a clinical and epidemiological analysis
Title | Transmission of rat hepatitis E virus infection to humans in Hong Kong: a clinical and epidemiological analysis |
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Authors | |
Keywords | rodent zoonosis public health epidemiology liver disease |
Issue Date | 2021 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ |
Citation | Hepatology, 2021, v. 73 n. 1, p. 10-22 How to Cite? |
Abstract | Background & 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 novel zoonosis in Hong Kong.
Approach & 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 immunosuppressed patients. Three patients had acute hepatitis, four had persistent hepatitis while 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. 7/186 (3·76%) rats tested positive for HEV‐C1. 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. |
Persistent Identifier | http://hdl.handle.net/10722/284101 |
ISSN | 2023 Impact Factor: 12.9 2023 SCImago Journal Rankings: 5.011 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Sridhar, S | - |
dc.contributor.author | Yip, CCY | - |
dc.contributor.author | Wu, S | - |
dc.contributor.author | Chew, NFS | - |
dc.contributor.author | Leung, KH | - |
dc.contributor.author | Chan, JFW | - |
dc.contributor.author | Zhao, PS | - |
dc.contributor.author | Chan, WM | - |
dc.contributor.author | Poon, RWS | - |
dc.contributor.author | Tsoi, HW | - |
dc.contributor.author | Cai, JP | - |
dc.contributor.author | Chan, HSY | - |
dc.contributor.author | Leung, AWS | - |
dc.contributor.author | Tse, CWS | - |
dc.contributor.author | Zee, JST | - |
dc.contributor.author | TSang, OTY | - |
dc.contributor.author | Cheng, VCC | - |
dc.contributor.author | Lau, SKP | - |
dc.contributor.author | Woo, PCY | - |
dc.contributor.author | Tsang, DNC | - |
dc.contributor.author | Yuen, KY | - |
dc.date.accessioned | 2020-07-20T05:56:06Z | - |
dc.date.available | 2020-07-20T05:56:06Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Hepatology, 2021, v. 73 n. 1, p. 10-22 | - |
dc.identifier.issn | 0270-9139 | - |
dc.identifier.uri | http://hdl.handle.net/10722/284101 | - |
dc.description.abstract | Background & 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 novel zoonosis in Hong Kong. Approach & 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 immunosuppressed patients. Three patients had acute hepatitis, four had persistent hepatitis while 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. 7/186 (3·76%) rats tested positive for HEV‐C1. 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. | - |
dc.language | eng | - |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ | - |
dc.relation.ispartof | Hepatology | - |
dc.rights | Postprint This is the peer reviewed version of the following article: [Hepatology, 2021, v. 73 n. 1, p. 10-22], which has been published in final form at [http://dx.doi.org/10.1002/hep.31138]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | - |
dc.subject | rodent | - |
dc.subject | zoonosis | - |
dc.subject | public health | - |
dc.subject | epidemiology | - |
dc.subject | liver disease | - |
dc.title | Transmission of rat hepatitis E virus infection to humans in Hong Kong: a clinical and epidemiological analysis | - |
dc.type | Article | - |
dc.identifier.email | Sridhar, S: sid8998@hku.hk | - |
dc.identifier.email | Wu, S: wss2017@hku.hk | - |
dc.identifier.email | Chew, NFS: chewnf@hku.hk | - |
dc.identifier.email | Leung, KH: khl17@hku.hk | - |
dc.identifier.email | Chan, JFW: jfwchan@hku.hk | - |
dc.identifier.email | Chan, WM: mbally@hku.hk | - |
dc.identifier.email | Tsoi, HW: hwtsoi@hkucc.hku.hk | - |
dc.identifier.email | Cai, JP: caijuice@hku.hk | - |
dc.identifier.email | Lau, SKP: skplau@hkucc.hku.hk | - |
dc.identifier.email | Woo, PCY: pcywoo@hkucc.hku.hk | - |
dc.identifier.email | Yuen, KY: kyyuen@hkucc.hku.hk | - |
dc.identifier.authority | Sridhar, S=rp02249 | - |
dc.identifier.authority | Chan, JFW=rp01736 | - |
dc.identifier.authority | Tsoi, HW=rp00439 | - |
dc.identifier.authority | Lau, SKP=rp00486 | - |
dc.identifier.authority | Woo, PCY=rp00430 | - |
dc.identifier.authority | Yuen, KY=rp00366 | - |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1002/hep.31138 | - |
dc.identifier.pmid | 31960460 | - |
dc.identifier.scopus | eid_2-s2.0-85081129563 | - |
dc.identifier.hkuros | 310921 | - |
dc.identifier.volume | 73 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | 10 | - |
dc.identifier.epage | 22 | - |
dc.identifier.eissn | 1527-3350 | - |
dc.identifier.isi | WOS:000576691300001 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 0270-9139 | - |