Rat Hepatitis E Virus (RHEV) in Mus musculus and Rattus norvegicus in Northwestern Italy.

Federica Di Profio1 Vittorio Sarchese1 Matteo Carnevale1 Serena Robetto2 Maria Lucia Mandola2 Chiara Nogarol2 Francesco Pellegrini3 Fulvio Marsilio1 Vito Martella3,4 Barbara Di Martino1
Affiliations 4 institutions
  1. Department of Veterinary Medicine, Università Degli Studi di Teramo, Teramo, Italy.
  2. Istituto Zooprofilattico Sperimentale del Piemonte, Della Liguria e Della Valle D'aosta, Turin, Italy.
  3. Department of Veterinary Medicine, University of Bari Aldo Moro, Bari, Italy.
  4. Department of Pharmacology and Toxicology, University of Veterinary Medicine, Budapest, Hungary.
Active Last checked 2026-10-11 03:30:14 Source: NCBI PubMed

Abstract

Hepatitis E virus (HEV) represents a major public health concern. Beyond the main zoonotic genotypes HEV-3 and HEV-4, with pigs and wild boars recognized as the primary reservoirs of infection, a genetically distinct hepevirus of rodent origin (species Rocahepevirus ratti, genotype C1) (rat HEV, RHEV) has recently been implicated in human hepatitis cases worldwide. Although several risk factors have been proposed, contact with rats has been documented in one human case only, and the sources and transmission routes of RHEV remain largely unclear. Of interest, RHEV RNA has recently been detected in farmed pigs, highlighting livestock environments as potential interspecies transmission interfaces. In light of these findings, we performed a molecular investigation for RHEV in rodents captured on farms raising different livestock species in Northwestern Italy (Piemonte region). A total of 98 rodents, collected on 32 livestock farms, were tested for RHEV by a combined molecular approach based on RHEV specific real-time reverse transcription (RT)-PCR assay and a pan-hepevirus heminested RT-PCR. Positive samples were further processed to attempt full-genome amplification. RHEV RNA was identified in a Norway rat (Rattus norvegicus) and in house mice (Mus musculus), with detection rates of 16.6% (1/6; 95% CI: 0.41-64.1) and 7.0% (6/86; 95% CI: 2.6-14.5), respectively. The positive rodents were captured in five livestock farms, raising cattle, goats, and poultry, located across three municipalities. The nearly full-length genome of a rat strain (RHEV/Rattus norvegicus/38129-22/ITA) was reconstructed. Pairwise nucleotide alignment showed high genetic relatedness of RHEV/Rattus norvegicus/38129-22/ITA with sequences previously identified in rodents and human patients, including those from European countries. The identification of infected rodents in livestock farms highlights RHEV circulation in rural environments, where interactions among rodents, domestic animals, and humans may be facilitated. Additional studies are necessary to elucidate RHEV transmission dynamics and assess public health implications.

Supporting text Virus Host Location
house mouse 2 Italy 23 rat 6 RHEV 2

Evidence records

5 total
Zoonotic Surveillance
4 records · 2 evidence types
Evidence type
3 records
OVE12339
Key finding

RHEV RNA was detected in a Norway rat (Rattus norvegicus) in Northwestern Italy with a detection rate of 16.6% (1/6).

Virus
Host
Location
Supporting text

RHEV RNA was identified in a Norway rat (Rattus norvegicus)... with detection rates of 16.6% (1/6; 95% CI: 0.41-64.1).

Method
RHEV specific real-time RT-PCR | pan-hepevirus heminested RT-PCR | full-genome amplification (attempted)
Sample type
samples tested for RHEV by RHEV specific real-time reverse transcription (RT)-PCR assay and a pan-hepevirus heminested RT-PCR
Geographic raw
Northwestern Italy (Piemonte region)
Country inferred
ITA
OVE12340
Key finding

RHEV RNA was detected in house mice (Mus musculus) in Northwestern Italy with a detection rate of 7.0% (6/86).

Virus
Host
Location
Supporting text

RHEV RNA was identified... in house mice (Mus musculus), with detection rates of 7.0% (6/86; 95% CI: 2.6-14.5).

Method
RHEV specific real-time RT-PCR | pan-hepevirus heminested RT-PCR | full-genome amplification (attempted)
Sample type
samples tested for RHEV by RHEV specific real-time reverse transcription (RT)-PCR assay and a pan-hepevirus heminested RT-PCR
Geographic raw
Northwestern Italy (Piemonte region)
Country inferred
ITA
OVE12341
Key finding

RHEV-positive rodents were captured on five livestock farms across three municipalities in Northwestern Italy.

Virus
Host
Location
Supporting text

The positive rodents were captured in five livestock farms, raising cattle, goats, and poultry, located across three municipalities.

Method
RHEV specific real-time RT-PCR | pan-hepevirus heminested RT-PCR
Sample type
rodent samples tested by RT-PCR assays
Geographic raw
five livestock farms | three municipalities | Northwestern Italy (Piemonte region)
Country inferred
ITA
Evidence type
1 records
OVE12343
Key finding

Detection of RHEV-positive rodents on livestock farms indicates circulation at a rural wildlife–livestock–human interface.

Virus
Host
Location
Supporting text

The identification of infected rodents in livestock farms highlights RHEV circulation in rural environments, where interactions among rodents, domestic animals, and humans may be facilitated.

Method
RHEV specific real-time reverse transcription (RT)-PCR | pan-hepevirus heminested RT-PCR | molecular investigation of rodents captured on livestock farms
Geographic raw
livestock farms | rural environments | Northwestern Italy (Piemonte region)
Country inferred
ITA
Genomic Evolution
1 records · 1 evidence types
Evidence type
1 records
OVE12342
Key finding

A nearly full-length rat RHEV genome from Northwestern Italy is highly related to previously reported rodent and human RHEV sequences, including European cases.

Virus
Host
Location
Not specified
Supporting text

The nearly full-length genome of a rat strain (RHEV/Rattus norvegicus/38129-22/ITA) was reconstructed. Pairwise nucleotide alignment showed high genetic relatedness of RHEV/Rattus norvegicus/38129-22/ITA with sequences previously identified in rodents and human patients, including those from European countries.

Genes or proteins
nearly full-length genome
Analysis methods
pairwise nucleotide alignment | comparative genomic analysis