Analyze Diet
Pathologie-biologie2008; 57(2); 188-196; doi: 10.1016/j.patbio.2008.04.006

Henipaviruses: a new family of emerging Paramyxoviruses.

Abstract: Paramyxoviruses have been implicated in both animal and human infections. Some viruses, such as Morbilliviruses are responsible for large-scale epidemics. However, there are limited observations of these viruses crossing the host species barrier in nature. In 1994, in Australia a fatal infection in horses and humans was identified to be caused by a new Paramyxovirus, Hendra virus (HeV), and in 1998 in Malaysia, a closely related virus, Nipah virus (NiV) was responsible for fatal infections in pigs and humans. These two viruses were sufficiently different from previously described Paramyxoviruses to create a new genus, Henipaviruses. The natural reservoir of these viruses was the fruit bat (Pteropus), which is found in regions extending from the western Pacific to the eastern coast of Africa. Serological studies have established that as many as half the fruit bats in colonies throughout these regions may have antibodies against this family of viruses. The availability of diagnostic reagents for Nipah virus in humans have identified infections in several countries including, Bangladesh, India and Indonesia. In some of these epidemics, mortality in humans exceeds 75%. Deforestation is probably responsible for fruit bats leaving their ecological niches and approaching farms and villages. The infection of humans and animals may occur via contaminated foods or in certain cases by animals to man. At present, only within close families has human-to-human transmission been proposed. Henipavirus infections are probably more widespread than it is at presently known and so it is important to have an intense monitoring for these diseases, especially in countries where large-scale deforestation is happening.
Publication Date: 2008-06-03 PubMed ID: 18511217DOI: 10.1016/j.patbio.2008.04.006Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Review

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This study revolves around the discovery, spread, and potential risk of Henipaviruses, a new genus of Paramyxoviruses causing fatal infections in horses, pigs, and humans. The research highlights the need for intense monitoring due to their widespread prevalence, notably in countries with significant deforestation.

Discovery of Henipaviruses

  • In 1994, a fatal infection affecting horses and humans in Australia was identified as a new Paramyxovirus named Hendra virus (HeV).
  • In 1998, a closely related virus called Nipah virus (NiV) caused lethal infections in pigs and humans in Malaysia.
  • Henipaviruses were formally introduced as a new genus, having significant differences from previously identified Paramyxoviruses.

Role of Fruit Bats as Natural Reservoirs

  • Fruit bats (Pteropus) are identified as the natural carriers of these viruses, found in regions expanding from the western Pacific to the eastern coast of Africa.
  • Available serological studies established that nearly half the fruit bat colonies throughout these regions may have antibodies against these viruses. It signifies their capacity to carry the infection without exhibiting symptoms.

Propagation and Human Impact of Henipavirus Infections

  • Human infections due to Nipah virus have been identified in several countries, including Bangladesh, India, and Indonesia, with mortality rates in some outbreaks exceeding 75%.
  • Henipavirus infections seem to be spreading more vastly than currently known. Transmission of the infection is likely to occur through contaminated foods or from animals to humans. However, human-to-human transmission is suggested only within immediate family members.

Deforestation and Virus Spread

  • The study suggested that large-scale deforestation might be causing fruit bats to leave their natural habitats and approach farmlands and villages, increasing the chances of virus exposure.
  • Massive deforestation may hence contribute to the transmission of Henipavirus infections, leading to potential outbreaks in humans and animals.
  • The paper calls for stringent monitoring for these diseases, especially in countries with extensive deforestation, to detect and prevent potential outbreaks.

Cite This Article

APA
Wild TF. (2008). Henipaviruses: a new family of emerging Paramyxoviruses. Pathol Biol (Paris), 57(2), 188-196. https://doi.org/10.1016/j.patbio.2008.04.006

Publication

ISSN: 0369-8114
NlmUniqueID: 0265365
Country: France
Language: English
Volume: 57
Issue: 2
Pages: 188-196

Researcher Affiliations

Wild, T F
  • Inserm U758, Immunobiology of viral infections, 69365 Lyon, France. fabian.wild@btinternet.com

MeSH Terms

  • Animals
  • Chiroptera / virology
  • Disease Outbreaks
  • Disease Transmission, Infectious
  • Henipavirus / isolation & purification
  • Henipavirus / pathogenicity
  • Henipavirus Infections / epidemiology
  • Henipavirus Infections / veterinary
  • Horse Diseases / virology
  • Horses
  • Humans
  • Malaysia / epidemiology

References

This article includes 58 references

Citations

This article has been cited 21 times.
  1. Wu X, Xiang R, Yang D, He X, Zhu L, Sun F, Li H, Pi N, Li Y. HRP-integrated CRISPR-Cas12a biosensor for rapid point-of-care detection of Langya henipavirus. iScience 2024 Dec 20;27(12):111466.
    doi: 10.1016/j.isci.2024.111466pubmed: 39758988google scholar: lookup
  2. Zhu W, Smith G, Pickering B, Banadyga L, Yang M. Enzyme-Linked Immunosorbent Assay Using Henipavirus-Receptor EphrinB2 and Monoclonal Antibodies for Detecting Nipah and Hendra Viruses. Viruses 2024 May 16;16(5).
    doi: 10.3390/v16050794pubmed: 38793674google scholar: lookup
  3. Findlay-Wilson S, Flett L, Salguero FJ, Ruedas-Torres I, Fotheringham S, Easterbrook L, Graham V, Dowall S. Establishment of a Nipah Virus Disease Model in Hamsters, including a Comparison of Intranasal and Intraperitoneal Routes of Challenge. Pathogens 2023 Jul 26;12(8).
    doi: 10.3390/pathogens12080976pubmed: 37623936google scholar: lookup
  4. Joshi J, Shah Y, Pandey K, Ojha RP, Joshi CR, Bhatt LR, Dumre SP, Acharya PR, Joshi HR, Rimal S, Shahi R, Pokharel D, Khadka KS, Dahal B, Nepal S, Dhami RS, Pant KP, Basnet R, Pandey BD. Possible high risk of transmission of the Nipah virus in South and South East Asia: a review. Trop Med Health 2023 Aug 10;51(1):44.
    doi: 10.1186/s41182-023-00535-7pubmed: 37559114google scholar: lookup
  5. Muzeniek T, Perera T, Siriwardana S, Bas D, Kaplan F, Öruc M, Becker-Ziaja B, Schwarz F, Premawansa G, Premawansa S, Perera I, Yapa W, Nitsche A, Kohl C. Detection of Alpha- and Betacoronaviruses in Miniopterus fuliginosus and Rousettus leschenaultii, two species of Sri Lankan Bats. Vaccines (Basel) 2021 Jun 15;9(6).
    doi: 10.3390/vaccines9060650pubmed: 34203592google scholar: lookup
  6. White RJ, Razgour O. Emerging zoonotic diseases originating in mammals: a systematic review of effects of anthropogenic land-use change. Mamm Rev 2020 Oct;50(4):336-352.
    doi: 10.1111/mam.12201pubmed: 32836691google scholar: lookup
  7. Gummow B. Challenges posed by new and re-emerging infectious diseases in livestock production, wildlife and humans. Livest Sci 2010 May;130(1):41-46.
    doi: 10.1016/j.livsci.2010.02.009pubmed: 32288869google scholar: lookup
  8. Eickmann M, Gravemann U, Handke W, Tolksdorf F, Reichenberg S, Müller TH, Seltsam A. Inactivation of three emerging viruses - severe acute respiratory syndrome coronavirus, Crimean-Congo haemorrhagic fever virus and Nipah virus - in platelet concentrates by ultraviolet C light and in plasma by methylene blue plus visible light. Vox Sang 2020 Apr;115(3):146-151.
    doi: 10.1111/vox.12888pubmed: 31930543google scholar: lookup
  9. Hedrick SM. Understanding Immunity through the Lens of Disease Ecology. Trends Immunol 2017 Dec;38(12):888-903.
    doi: 10.1016/j.it.2017.08.001pubmed: 28882454google scholar: lookup
  10. Lacroix A, Duong V, Hul V, San S, Davun H, Omaliss K, Chea S, Hassanin A, Theppangna W, Silithammavong S, Khammavong K, Singhalath S, Afelt A, Greatorex Z, Fine AE, Goldstein T, Olson S, Joly DO, Keatts L, Dussart P, Frutos R, Buchy P. Diversity of bat astroviruses in Lao PDR and Cambodia. Infect Genet Evol 2017 Jan;47:41-50.
    doi: 10.1016/j.meegid.2016.11.013pubmed: 27871796google scholar: lookup
  11. Muzyka D, Pantin-Jackwood M, Stegniy B, Rula O, Bolotin V, Stegniy A, Gerilovych A, Shutchenko P, Stegniy M, Koshelev V, Maiorova K, Tkachenko S, Muzyka N, Usova L, Afonso CL. Wild bird surveillance for avian paramyxoviruses in the Azov-black sea region of Ukraine (2006 to 2011) reveals epidemiological connections with Europe and Africa. Appl Environ Microbiol 2014 Sep;80(17):5427-38.
    doi: 10.1128/AEM.00733-14pubmed: 24973063google scholar: lookup
  12. Sendow I, Ratnawati A, Taylor T, Adjid RM, Saepulloh M, Barr J, Wong F, Daniels P, Field H. Nipah virus in the fruit bat Pteropus vampyrus in Sumatera, Indonesia. PLoS One 2013;8(7):e69544.
    doi: 10.1371/journal.pone.0069544pubmed: 23894501google scholar: lookup
  13. DeBuysscher BL, de Wit E, Munster VJ, Scott D, Feldmann H, Prescott J. Comparison of the pathogenicity of Nipah virus isolates from Bangladesh and Malaysia in the Syrian hamster. PLoS Negl Trop Dis 2013;7(1):e2024.
    doi: 10.1371/journal.pntd.0002024pubmed: 23342177google scholar: lookup
  14. Caignard G, Lucas-Hourani M, Dhondt KP, Labernardière JL, Petit T, Jacob Y, Horvat B, Tangy F, Vidalain PO. The V protein of Tioman virus is incapable of blocking type I interferon signaling in human cells. PLoS One 2013;8(1):e53881.
    doi: 10.1371/journal.pone.0053881pubmed: 23342031google scholar: lookup
  15. Weiss S, Nowak K, Fahr J, Wibbelt G, Mombouli JV, Parra HJ, Wolfe ND, Schneider BS, Leendertz FH. Henipavirus-related sequences in fruit bat bushmeat, Republic of Congo. Emerg Infect Dis 2012 Sep;18(9):1536-7.
    doi: 10.3201/eid1809.111607pubmed: 22935105google scholar: lookup
  16. Pallister J, Middleton D, Wang LF, Klein R, Haining J, Robinson R, Yamada M, White J, Payne J, Feng YR, Chan YP, Broder CC. A recombinant Hendra virus G glycoprotein-based subunit vaccine protects ferrets from lethal Hendra virus challenge. Vaccine 2011 Aug 5;29(34):5623-30.
    doi: 10.1016/j.vaccine.2011.06.015pubmed: 21689706google scholar: lookup
  17. Vigant F, Lee B. Hendra and nipah infection: pathology, models and potential therapies. Infect Disord Drug Targets 2011 Jun;11(3):315-36.
    doi: 10.2174/187152611795768097pubmed: 21488828google scholar: lookup
  18. Bowden TA, Jones EY, Stuart DI. Cells under siege: viral glycoprotein interactions at the cell surface. J Struct Biol 2011 Aug;175(2):120-6.
    doi: 10.1016/j.jsb.2011.03.016pubmed: 21440638google scholar: lookup
  19. Miller PJ, Afonso CL, Spackman E, Scott MA, Pedersen JC, Senne DA, Brown JD, Fuller CM, Uhart MM, Karesh WB, Brown IH, Alexander DJ, Swayne DE. Evidence for a new avian paramyxovirus serotype 10 detected in rockhopper penguins from the Falkland Islands. J Virol 2010 Nov;84(21):11496-504.
    doi: 10.1128/JVI.00822-10pubmed: 20702635google scholar: lookup
  20. Chiang CF, Lo MK, Rota PA, Spiropoulou CF, Rollin PE. Use of monoclonal antibodies against Hendra and Nipah viruses in an antigen capture ELISA. Virol J 2010 Jun 3;7:115.
    doi: 10.1186/1743-422X-7-115pubmed: 20525276google scholar: lookup
  21. Bowden TA, Crispin M, Harvey DJ, Aricescu AR, Grimes JM, Jones EY, Stuart DI. Crystal structure and carbohydrate analysis of Nipah virus attachment glycoprotein: a template for antiviral and vaccine design. J Virol 2008 Dec;82(23):11628-36.
    doi: 10.1128/JVI.01344-08pubmed: 18815311google scholar: lookup