Literature detail

Natural Hendra Virus Infection in Flying-Foxes - Tissue Tropism and Risk Factors.

Lauren K Goldspink1 Daniel W Edson1 Miranda E Vidgen1 John Bingham2 Hume E Field3,4 Craig S Smith1
Affiliations 4 institutions
  1. Queensland Centre for Emerging Infectious Diseases, Biosecurity Queensland, Department of Agriculture and Fisheries, Coopers Plains, Queensland, Australia.
  2. Australian Animal Health Laboratory, Commonwealth Scientific and Industrial Research Organisation, East Geelong, Victoria, Australia.
  3. Queensland Centre for Emerging Infectious Diseases, Biosecurity Queensland, Department of Agriculture and Fisheries, Coopers Plains, Queensland, Australia
  4. EcoHealth Alliance, New York, New York, United States of America.
PMID 26060997 2015 PLoS One eng epublish
PubMed DOI Browse context

Article

Publication summary

Hendra virus (HeV) is a lethal zoonotic agent that emerged in 1994 in Australia. Pteropid bats (flying-foxes) are the natural reservoir. To date, HeV has spilled over from flying-foxes to horses on 51 known occasions, and from infected horses to close-contact humans on seven occasions. We undertook screening of archived bat tissues for HeV by reverse transcription quantitative polymerase chain reaction (RT-qPCR). Tissues were tested from 310 bats including 295 Pteropodiformes and 15 Vespertilioniformes. HeV was detected in 20 individual flying-foxes (6.4%) from various tissues including spleen, kidney, liver, lung, placenta and blood components. Detection was significantly higher in Pteropus Alecto and P. conspicillatus, identifying species as a risk factor for infection. Further, our findings indicate that HeV has a predilection for the spleen, suggesting this organ plays an important role in HeV infection. The lack of detections in the foetal tissues of HeV-positive females suggests that vertical transmission is not a regular mode of transmission in naturally infected flying-foxes, and that placental and foetal tissues are not a major source of infection for horses. A better understanding of HeV tissue tropism will strengthen management of the risk of spillover from flying-foxes to horses and ultimately humans.

Viral Tropism Animals Chiroptera Female Hendra Virus Henipavirus Infections Male Pregnancy Reverse Transcriptase Polymerase Chain Reaction Risk Factors Species Specificity Zoonoses

Structured evidence records

Evidence records

3 total
2 records
Extraction confidence 0.95
Key finding

Hendra virus has spilled over from flying-foxes to horses and subsequently from infected horses to humans in Australia.

Virus
Location
Supporting text

HeV has spilled over from flying-foxes to horses on 51 known occasions, and from infected horses to close-contact humans on seven occasions.

Method
reverse transcription quantitative polymerase chain reaction
Study design
field surveillance
Transmission direction
animal-to-human
Geographic raw
Australia
Country inferred
Australia
Extraction confidence 0.95
Key finding

Hendra virus transmission from infected horses to humans has occurred on seven known occasions.

Virus
Location
Supporting text

HeV has spilled over from flying-foxes to horses on 51 known occasions, and from infected horses to close-contact humans on seven occasions.

Method
reverse transcription quantitative polymerase chain reaction
Study design
field surveillance
Transmission direction
animal-to-human
Geographic raw
Australia
Country inferred
Australia
1 records
Extraction confidence 0.96
Key finding

Hendra virus was detected by RT-qPCR in archived tissues from flying-foxes in Australia, providing surveillance evidence of infection prevalence and tissue tropism in the reservoir host.

Virus
Location
Supporting text

We undertook screening of archived bat tissues for HeV by reverse transcription quantitative polymerase chain reaction (RT-qPCR). Tissues were tested from 310 bats including 295 Pteropodiformes and 15 Vespertilioniformes. HeV was detected in 20 individual flying-foxes (6.4%) from various tissues including spleen, kidney, liver, lung, placenta and blood components.

Method
RT-qPCR
Sample type
spleen; kidney; liver; lung; placenta; blood components
Geographic raw
Australia
Country inferred
Australia