Host hybridization enabled the emergence of a reassorted hantavirus lineage.

Anton Labutin1 Nadine Ritter2,3,4 Guiscard Seebohm2 Gerald Heckel1
Affiliations 4 institutions
  1. Institute of Ecology and Evolution, University of Bern, Bern, Switzerland.
  2. Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany.
  3. Chembion, University of Münster, Münster, Germany.
  4. Department of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.

Abstract

The exchange of genetic material between individuals is a key driver of evolution and diversification across most branches of life. Segmented viruses can exchange genetic material through reassortment of genomic segments. New viral strains that emerge from reassortments can have greater infection ranges and higher virulence, although concrete examples of the adaptive advantages of reassortants in nature apart from influenza remain rare. We studied here the evolutionary history and consequences of reassortment in Tula orthohantavirus (TULV) in a hybrid zone between evolutionary lineages of its reservoir host, the common vole (Microtus arvalis). Across 58 trapping sites and 127 infected voles, we detected 27 TULV reassortants in a 12.5 km broad zone at the contact of the parental TULV clades, resembling a viral hybrid zone concordant with the hosts'. Phylogenomic analyses revealed three independent reassortment events, but most of the host hybrid zone was dominated by a single strain with a reassorted M-Segment, which encodes the surface glycoprotein. We detected clade-specific variation in the glycoprotein's N-terminal region consisting of five residues, two of which showed evidence of positive selection. In silico 3D modeling of seven glycoproteins confirmed that this N-terminal region has a unique and specific structure for each TULV clade and the dominant reassortants and is the only structurally variable region of the TULV glycoprotein. Our findings suggest that reassortment between the parental TULV clades in the contact region has resulted in a transgressive virus phenotype potentially adapted to hybrid hosts. This demonstrates the potential of zones of hybridization for the emergence of new virus strains with novel evolutionary trajectories.

Supporting text Virus Host Location

Evidence records

7 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE11848
Key finding

Tula orthohantavirus (TULV) was detected in 127 infected voles across 58 trapping sites, including 27 reassortant TULV detections within a 12.5 km hybrid zone.

Virus
Host
Location
Supporting text

Across 58 trapping sites and 127 infected voles, we detected 27 TULV reassortants in a 12.5 km broad zone at the contact of the parental TULV clades

Method
phylogenomic analyses
Geographic raw
a 12.5 km broad zone at the contact of the parental TULV clades
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE11849
Key finding

TULV clades and dominant reassortants exhibit clade-specific N-terminal glycoprotein variation, including five residues (two under positive selection) that form uniquely structured regions, implicating adaptive glycoprotein changes.

Virus
Host
Not specified
Location
Not specified
Supporting text

We detected clade-specific variation in the glycoprotein's N-terminal region consisting of five residues, two of which showed evidence of positive selection. In silico 3D modeling of seven glycoproteins confirmed that this N-terminal region has a unique and specific structure for each TULV clade and the dominant reassortants and is the only structurally variable region of the TULV glycoprotein.

Genes or proteins
glycoprotein | M-Segment
Mechanism types
receptor binding | host-range expansion | tissue tropism | transmission fitness
Genomic Evolution
5 records · 2 evidence types
Evidence type
1 records
OVE11847
Key finding

Phylogenomics identified three independent reassortment events in Tula orthohantavirus, with a dominant lineage carrying a reassorted M-segment in the host hybrid zone.

Virus
Host
Not specified
Location
Not specified
Supporting text

Phylogenomic analyses revealed three independent reassortment events, but most of the host hybrid zone was dominated by a single strain with a reassorted M-Segment, which encodes the surface glycoprotein.

Event type
reassortment
Genes or segments
M-Segment | glycoprotein
Evidence type
4 records
OVE11850
Key finding

Phylogenomic analyses show three independent reassortment events in Tula orthohantavirus with dominance of a lineage carrying a reassorted M segment across a host hybrid zone.

Virus
Host
Context pending
Location
Not specified
Supporting text

Phylogenomic analyses revealed three independent reassortment events, but most of the host hybrid zone was dominated by a single strain with a reassorted M-Segment, which encodes the surface glycoprotein.

Genes or proteins
M-Segment | glycoprotein
Analysis methods
Phylogenomic analyses
OVE11853
Key finding

A viral hybrid zone of TULV reassortants spans a ~12.5 km region concordant with the host hybrid zone, with 27 reassortant genomes detected among 127 infected voles from 58 sites.

Virus
Host
Location
Not specified
Supporting text

Across 58 trapping sites and 127 infected voles, we detected 27 TULV reassortants in a 12.5 km broad zone at the contact of the parental TULV clades, resembling a viral hybrid zone concordant with the hosts'.

Analysis methods
phylogeographic analysis | clade-based phylogenetic analysis
OVE11851
Key finding

Clade-specific variation in the TULV glycoprotein N-terminal region involves five residues, with two sites showing evidence of positive selection.

Virus
Host
Not specified
Location
Not specified
Supporting text

We detected clade-specific variation in the glycoprotein's N-terminal region consisting of five residues, two of which showed evidence of positive selection.

Genes or proteins
glycoprotein | N-terminal region
Analysis methods
positive selection analysis
OVE11852
Key finding

In silico 3D modeling shows the glycoprotein N-terminal region is uniquely structured for each TULV clade and dominant reassortants and is the only structurally variable glycoprotein region.

Virus
Host
Not specified
Location
Not specified
Supporting text

In silico 3D modeling of seven glycoproteins confirmed that this N-terminal region has a unique and specific structure for each TULV clade and the dominant reassortants and is the only structurally variable region of the TULV glycoprotein.

Genes or proteins
glycoprotein | N-terminal region
Analysis methods
in silico 3D modeling | structural comparative analysis