Identification and genetic characterization of a distinct genotype of Puumala orthohantavirus in Hebei Province, China.

Yanan Cai1,2 Yamei Wei2,3 Guoyi Du4 Xinyang Zhang2 Zhenkun Wang1 Zhengguang Wang5 Zhanying Han2,3 Yanbo Zhang2,3 Yonggang Xu2,3 Xu Han2,3 Jiandong Li6 Qi Li1,2
Affiliations 6 institutions
  1. School of Public Health, Hebei Medical University, Shijiazhuang, China.
  2. Institute for Viral Disease Control and Prevention, Hebei Provincial Center for Disease Control and Prevention, Shijiazhuang, China.
  3. Hebei Key Laboratory of Pathogens and Epidemiology of Infectious Diseases, Hebei Provincial Center for Disease Control and Prevention, Shijiazhuang, China.
  4. Hebei Provincial Institute for Plague Control, Zhangjiakou, China.
  5. School of Public Health, Hebei University, Baoding, China.
  6. National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.

Abstract

Orthohantavirus infections pose a significant threat to human health, while numerous orthohantaviruses have been identified, suspected viral infections remain undiagnosed in the world, which highlights the need for further identification and characterization of viruses circulating in humans and host animals. In this study, viral metagenomics was utilized to investigate orthohantaviruses present in tissue samples collected from rodents trapped at the Bashang Grassland of Hebei Province, China. A total of 145 wild rodents belonging to six species were captured in the study area, and 725 tissue samples (lung, liver, kidney, spleen, gut) were collected in 2024. A Puumala orthohantavirus (PUUV), named Guyuan strain, was identified in Myodes rufocanus, with a positive rate of 0.69%. The complete genomic sequences of the L, M, and S segments were obtained and confirmed by Sanger sequencing. Phylogenetic analysis of these genomic sequences with those of other orthohantavirus species showed that the L, M, and S segments clustered with PUUV genomic sequences, while sharing a nucleotide sequence similarity of 81.2%, 80.2%, and 84.3% with previously characterized reference viral strains Kitahiyama128L, Tobetsu_04, and Baltic/205 Cg, respectively. Amino acid homology analysis demonstrated that the sequences exhibited the highest identity to PUUV Hokkaido strain at a level of 95.4%, 94.6%, and 97.0% respectively. Viral particles were observed in lung and kidney tissues using transmission electron microscopy, and viral protein antigen was detected in viral RNA-positive lung, liver, and kidney tissues through immunofluorescence assay with antibodies against the PUUV nucleocapsid protein, thereby confirming the virus's multiorgan tropism. The results demonstrated that a distinct genotype of PUUV was circulating in rodents in the study areas, which may have implications for zoonotic transmission surveillance and public health management in Hebei Province.

Supporting text Virus Host Location
Genotype 137 Puumala virus 3 Rodent Diseases 28 Animals 1948 Arvicolinae 16 China 229 Genome, Viral 317 Phylogeny 805 RNA, Viral 193 Rodentia 51

Evidence records

4 total
Zoonotic Surveillance
3 records · 2 evidence types
Evidence type
2 records
OVE11042
Key finding

A Puumala orthohantavirus (Guyuan strain) was detected in Myodes rufocanus rodents collected in Hebei Province, China.

Virus
Host
Location
Supporting text

In this study, viral metagenomics was utilized to investigate orthohantaviruses present in tissue samples collected from rodents trapped at the Bashang Grassland of Hebei Province, China. A Puumala orthohantavirus (PUUV), named Guyuan strain, was identified in Myodes rufocanus, with a positive rate of 0.69%.

Method
viral metagenomics | Sanger sequencing
Sample type
tissue samples
Geographic raw
Hebei Province
Country inferred
CHN
OVE11043
Key finding

Puumala orthohantavirus antigen and viral particles were detected in multiple organs of Myodes rufocanus by immunofluorescence and electron microscopy, showing multiorgan tropism.

Virus
Host
Not specified
Location
Not specified
Supporting text

Viral particles were observed in lung and kidney tissues using transmission electron microscopy, and viral protein antigen was detected in viral RNA-positive lung, liver, and kidney tissues through immunofluorescence assay with antibodies against the PUUV nucleocapsid protein, thereby confirming the virus's multiorgan tropism.

Method
transmission electron microscopy | immunofluorescence assay
Sample type
lung tissue | liver tissue | kidney tissue
Evidence type
1 records
OVE11045
Key finding

A distinct genotype of Puumala orthohantavirus was found to be circulating in rodents in Hebei Province, indicating ecological maintenance of the virus in local rodent populations.

Virus
Host
Location
Supporting text

The results demonstrated that a distinct genotype of PUUV was circulating in rodents in the study areas, which may have implications for zoonotic transmission surveillance and public health management in Hebei Province.

Method
viral metagenomics | phylogenetic analysis | transmission electron microscopy | immunofluorescence assay
Sample type
tissue samples (lung, liver, kidney, spleen, gut)
Geographic raw
Hebei Province
Country inferred
CHN
Genomic Evolution
1 records · 1 evidence types
Evidence type
1 records
OVE11044
Key finding

Phylogenetic analysis showed that the Puumala orthohantavirus Guyuan strain identified in Myodes rufocanus from Hebei Province represents a distinct genotype clustering within the PUUV lineage but with only about 80–84% nucleotide identity to known reference strains.

Virus
Host
Location
Not specified
Supporting text

A Puumala orthohantavirus (PUUV), named Guyuan strain, was identified in Myodes rufocanus, with a positive rate of 0.69%. Phylogenetic analysis of these genomic sequences with those of other orthohantavirus species showed that the L, M, and S segments clustered with PUUV genomic sequences, while sharing a nucleotide sequence similarity of 81.2%, 80.2%, and 84.3% with previously characterized reference viral strains Kitahiyama128L, Tobetsu_04, and Baltic/205 Cg, respectively.

Genes or proteins
L segment | M segment | S segment
Analysis methods
phylogenetic analysis | sequence similarity comparison