Jump to content

Spillover infection

From Wikipedia, the free encyclopedia

Spillover infection, also known as pathogen spillover and spillover event, occurs when a reservoir population with a high pathogen prevalence comes into contact with a novel host population. The pathogen is transmitted from the reservoir population and may or may not be transmitted within the host population.[1] Due to climate change and land use expansion, the risk of viral spillover is predicted to significantly increase.[2][3]

Spillover zoonoses

[edit]
The fruit bat is believed to be the zoonotic agent responsible for the spillover of the Ebola virus.

Spillover is a common event; in fact, more than two-thirds of human viruses are zoonotic.[4][5] Most spillover events result in self-limited cases with no further human-to-human transmission, as occurs, for example, with rabies, anthrax, histoplasmosis or hydatidosis. Other zoonotic pathogens are able to be transmitted by humans to produce secondary cases and even to establish limited chains of transmission. Some examples are the Ebola and Marburg filoviruses, the MERS and SARS coronaviruses and some avian flu viruses. Finally, some spillover events can result in the final adaptation of the microbe to humans, who can become a new stable reservoir, as occurred with the HIV virus resulting in the AIDS epidemic and with SARS-CoV-2 resulting in the COVID-19 pandemic.[5]

If the history of mutual adaptation is long enough, permanent host-microbe associations can be established resulting in co-evolution, and even permanent integration of the microbe genome with the human genome, as is the case of endogenous viruses.[6] The closer the two target host species are in phylogenetic terms, the easier it is for microbes to overcome the biological barrier to produce successful spillovers.[1] For this reason, other mammals are the main source of zoonotic agents for humans. For example, in the case of the Ebola virus, fruit bats are the hypothesized zoonotic agent.[7]

During the late 20th century, zoonotic spillover increased as the environmental impact of agriculture promoted increased land use and deforestation, changing wildlife habitat. As species shift their geographic range in response to climate change, the risk of zoonotic spillover is predicted to substantially increase, particularly in tropical regions that are experiencing rapid warming.[8] As forested areas of land are cleared for human use, there is increased proximity and interaction between wild animals and humans thereby increasing the potential for exposure.[9]

Intraspecies spillover

[edit]
The bumblebee is a potential reservoir for several pollinator parasites.

Commercially bred bumblebees used to pollinate greenhouses can be reservoirs for several pollinator parasites including the protozoans Crithidia bombi, and Apicystis bombi,[10] the microsporidians Nosema bombi and Nosema ceranae,[10][11] plus viruses such as Deformed wing virus and the tracheal mites Locustacarus buchneri.[11] Commercial bees that escape the greenhouse environment may then infect wild bee populations. Infection may be via direct interactions between managed and wild bees or via shared flower use and contamination.[12][13] One study found that half of all wild bees found near greenhouses were infected with C. bombi. Rates and incidence of infection decline dramatically the further away from the greenhouses where the wild bees are located.[14][15] Instances of spillover between bumblebees are well documented across the world, particularly in Japan, North America, and the United Kingdom.[16][17]

Examples of Spillover Zoonosis
Disease Reservoir
Hepatitis E Wild Boar[10]
Ebola Fruit Bats[11]
HIV/AIDS Chimpanzee[12]
COVID-19 Bats[28]

Causes of spillover

[edit]

Zoonotic spillover is a relatively uncommon but incredibly dangerous natural phenomenon—as is evidenced by the Ebola epidemic and Coronavirus pandemic. For zoonotic spillover to occur, several important factors have to occur in tandem.[1] Such factors include altered ecological niches, epidemiological susceptibility, and the natural behavior of pathogens and novel host or spillover host species.[29] By suggesting that the natural behavior of pathogens and host species impacts zoonotic spillover, simple Darwinian theories are being referenced. As with all species, a pathogen's main goal is to survive. When a stressor puts pressure on the survival of the pathogenic species, it will have to adapt to said stressor in order to survive.[30] For example, the ecological niche of the novel host may be subject to a lack of food which leads to a decrease in the novel host population. In order for a virus to replicate, it must invade a eukaryotic organism.[31] When the novel eukaryotic organism is not available for the virus to infect, it must jump to another host.[30] In order for the virus to make the jump to the spillover host, the spillover host must be epidemiologically susceptible to this virus. Although it is not well understood what makes one spillover host "better" than another host, it is known that the susceptibility has to do with the shedding rate of the virus, how well the virus survives and moves while not within a host, the genotypic similarities between the novel and spillover hosts, and the behavior of the spillover host that leads to contact with a high dose of the virus.[1]

See also

[edit]

References

[edit]
  1. ^ a b c d Woolhouse, Mark; Scott, Fiona; Hudson, Zoe; Howey, Richard; Chase-Topping, Margo (2012). "Human viruses: Discovery and emergence". Philosophical Transactions of the Royal Society B: Biological Sciences. 367 (1604): 2864–2871. doi:10.1098/rstb.2011.0354. PMC 3427559. PMID 22966141.
  2. ^ Wolfe, Nathan D.; Dunavan, Claire Panosian; Diamond, Jared (May 2007). "Origins of major human infectious diseases". Nature. 447 (7142): 279–283. Bibcode:2007Natur.447..279W. doi:10.1038/nature05775. ISSN 1476-4687. PMC 7095142. PMID 17507975.
  3. ^ Ebola. (2014). National Center for Emerging and Zoonotic Infectious Diseases, Division of High-Consequence Pathogens and Pathology, Department of Health & Human Services, CDC.
  4. ^ Graystock, P; Yates, K; Evison, SEF; Darvill, B; Goulson, D; Hughes, WOH (2013). "The Trojan hives: pollinator pathogens, imported and distributed in bumblebee colonies". Journal of Applied Ecology. 50 (5): 1207–15. Bibcode:2013JApEc..50.1207G. doi:10.1111/1365-2664.12134. S2CID 3937352.
  5. ^ a b Sachman-Ruiz, Bernardo; Narváez-Padilla, Verónica; Reynaud, Enrique (2015-03-10). "Commercial Bombus impatiens as reservoirs of emerging infectious diseases in central México". Biological Invasions. 17 (7): 2043–53. Bibcode:2015BiInv..17.2043S. doi:10.1007/s10530-015-0859-6. ISSN 1387-3547.
  6. ^ Durrer, Stephan; Schmid-Hempel, Paul (1994-12-22). "Shared Use of Flowers Leads to Horizontal Pathogen Transmission". Proceedings of the Royal Society of London B: Biological Sciences. 258 (1353): 299–302. Bibcode:1994RSPSB.258..299D. doi:10.1098/rspb.1994.0176. ISSN 0962-8452. S2CID 84926310.
  7. ^ Graystock, Peter; Goulson, Dave; Hughes, William O. H. (2015-08-22). "Parasites in bloom: flowers aid dispersal and transmission of pollinator parasites within and between bee species". Proceedings of the Royal Society B: Biological Sciences. 282 (1813): 20151371. doi:10.1098/rspb.2015.1371. ISSN 0962-8452. PMC 4632632. PMID 26246556.
  8. ^ Otterstatter, MC; Thomson, JD (2008). "Does Pathogen Spillover from Commercially Reared Bumble Bees Threaten Wild Pollinators?". PLOS ONE. 3 (7): e2771. Bibcode:2008PLoSO...3.2771O. doi:10.1371/journal.pone.0002771. PMC 2464710. PMID 18648661.
  9. ^ Graystock, Peter; Goulson, Dave; Hughes, William O.H. (2014). "The relationship between managed bees and the prevalence of parasites in bumblebees". PeerJ. 2: e522. doi:10.7717/peerj.522. PMC 4137657. PMID 25165632.
  10. ^ a b c Anheyer-Behmenburg, Helena E.; Szabo, Kathrin; Schotte, Ulrich; Binder, Alfred; Klein, Günter; Johne, Reimar (2017). "Hepatitis E Virus in Wild Boars and Spillover Infection in Red and Roe Deer, Germany, 2013–2015". Emerging Infectious Diseases. 23 (1): 130–133. doi:10.3201/eid2301.161169. PMC 5176221. PMID 27983488.
  11. ^ a b c Mursel, Sena; Alter, Nathaniel; Slavit, Lindsay; Smith, Anna; Bocchini, Paolo; Buceta, Javier (2022). "Estimation of Ebola's spillover infection exposure in Sierra Leone based on sociodemographic and economic factors". PLOS ONE. 17 (9): e0271886. arXiv:2109.15313. Bibcode:2022PLoSO..1771886M. doi:10.1371/journal.pone.0271886. PMC 9436100. PMID 36048780.
  12. ^ a b "About HIV/AIDS | HIV Basics | HIV/AIDS | CDC". www.cdc.gov. 2022-06-30. Retrieved 2022-12-08.
  13. ^ Graystock, Peter; Goulson, Dave; Hughes, William O. H. (2015-08-22). "Parasites in bloom: flowers aid dispersal and transmission of pollinator parasites within and between bee species". Proceedings of the Royal Society B: Biological Sciences. 282 (1813): 20151371. doi:10.1098/rspb.2015.1371. ISSN 0962-8452. PMC 4632632. PMID 26246556.
  14. ^ Otterstatter, Michael C.; Thomson, James D. (2008-07-23). Adler, Frederick R. (ed.). "Does Pathogen Spillover from Commercially Reared Bumble Bees Threaten Wild Pollinators?". PLOS ONE. 3 (7): e2771. Bibcode:2008PLoSO...3.2771O. doi:10.1371/journal.pone.0002771. ISSN 1932-6203. PMC 2464710. PMID 18648661.
  15. ^ Graystock, Peter; Goulson, Dave; Hughes, William O.H. (2014-08-12). "The relationship between managed bees and the prevalence of parasites in bumblebees". PeerJ. 2: e522. doi:10.7717/peerj.522. ISSN 2167-8359. PMC 4137657. PMID 25165632.
  16. ^ Graystock, Peter; Blane, Edward J.; McFrederick, Quinn S.; Goulson, Dave; Hughes, William O.H. (April 2016). "Do managed bees drive parasite spread and emergence in wild bees?". International Journal for Parasitology: Parasites and Wildlife. 5 (1): 64–75. doi:10.1016/j.ijppaw.2015.10.001. PMC 5439461. PMID 28560161.
  17. ^ Tlak Gajger, Ivana; Šimenc, Laura; Toplak, Ivan (2021-06-25). "The First Detection and Genetic Characterization of Four Different Honeybee Viruses in Wild Bumblebees from Croatia". Pathogens. 10 (7): 808. doi:10.3390/pathogens10070808. ISSN 2076-0817. PMC 8308666. PMID 34202101.
  18. ^ Valencak, Teresa G.; Csiszar, Anna; Szalai, Gabor; Podlutsky, Andrej; Tarantini, Stefano; Fazekas-Pongor, Vince; Papp, Magor; Ungvari, Zoltan (October 2021). "Animal reservoirs of SARS-CoV-2: calculable COVID-19 risk for older adults from animal to human transmission". GeroScience. 43 (5): 2305–2320. doi:10.1007/s11357-021-00444-9. ISSN 2509-2723. PMC 8404404. PMID 34460063.
  19. ^ Lawler, Odette K; Allan, Hannah L; Baxter, Peter W J; Castagnino, Romi; Tor, Marina Corella; Dann, Leah E; Hungerford, Joshua; Karmacharya, Dibesh; Lloyd, Thomas J; López-Jara, María José; Massie, Gloeta N; Novera, Junior; Rogers, Andrew M; Kark, Salit (November 2021). "The COVID-19 pandemic is intricately linked to biodiversity loss and ecosystem health". The Lancet. Planetary Health. 5 (11): e840 – e850. doi:10.1016/S2542-5196(21)00258-8. PMC 8580505. PMID 34774124. The current weight of evidence suggests that SARS-CoV-2, or its progenitor, probably emerged in humans from a zoonotic source in Wuhan, China, where it was first identified in 2019. Although evidence on the origins of SARS-CoV-2 are inconclusive, bats have been suggested to be the most probable evolutionary source for the virus."
  20. ^ Castelo-Branco, D.S.C.M.; Nobre, J.A.; Souza, P.R.H.; Diógenes, E.M.; Guedes, G.M.M.; Mesquita, F.P.; Souza, P.F.N.; Rocha, M.F.G.; Sidrim, J.J.C.; Cordeiro, R.A.; Montenegro, R.C. (February 2023). "Role of Brazilian bats in the epidemiological cycle of potentially zoonotic pathogens". Microbial Pathogenesis. 177: 106032. doi:10.1016/j.micpath.2023.106032. ISSN 0882-4010. PMID 36804526. S2CID 257015965. The pandemic of Coronavirus disease (COVID-19) has highlighted bats as reservoirs of coronaviruses that cause severe respiratory diseases in humans and, frequently, in other animals. However, despite the spillover events of SARS-CoV and MERS-CoV, the implication of bats as natural reservoirs of the ancient virus of SARS-CoV-2 is, to date, unconfirmed, as only closely related SARS-like viruses have been detected by genomic sequencing and little is known about the mechanisms of host switch from bats to humans.
  21. ^ Yuan, Shu; Jiang, Si-Cong; Li, Zi-Lin (9 June 2020). "Analysis of Possible Intermediate Hosts of the New Coronavirus SARS-CoV-2". Frontiers in Veterinary Science. 7: 379. doi:10.3389/fvets.2020.00379. eISSN 2297-1769. PMC 7297130. PMID 32582786.
  22. ^ a b Zhou, Peng; Shi, Zheng-Li (8 January 2021). "SARS-CoV-2 spillover events". Science. 371 (6525): 120–122. Bibcode:2021Sci...371..120Z. doi:10.1126/science.abf6097. eISSN 1095-9203. ISSN 0036-8075. PMID 33414206. S2CID 231138544.
  23. ^ Oude Munnink, Bas B.; Sikkema, Reina S.; Nieuwenhuijse, David F.; Molenaar, Robert Jan; Munger, Emmanuelle; Molenkamp, Richard; van der Spek, Arco; Tolsma, Paulien; Rietveld, Ariene; Brouwer, Miranda; Bouwmeester-Vincken, Noortje; Harders, Frank; Hakze-van der Honing, Renate; Wegdam-Blans, Marjolein C. A.; Bouwstra, Ruth J.; GeurtsvanKessel, Corine; van der Eijk, Annemiek A.; Velkers, Francisca C.; Smit, Lidwien A. M.; Stegeman, Arjan; van der Poel, Wim H. M.; Koopmans, Marion P. G. (8 January 2021). "Transmission of SARS-CoV-2 on mink farms between humans and mink and back to humans". Science. 371 (6525): 172–177. Bibcode:2021Sci...371..172O. doi:10.1126/science.abe5901. eISSN 1095-9203. ISSN 0036-8075. PMC 7857398. PMID 33172935.
  24. ^ Singh, Devika; Yi, Soojin V. (April 2021). "On the origin and evolution of SARS-CoV-2". Experimental & Molecular Medicine. 53 (4): 537–547. doi:10.1038/s12276-021-00604-z. eISSN 2092-6413. ISSN 1226-3613. PMC 8050477. PMID 33864026.
  25. ^ Wrobel, Antoni G.; Benton, Donald J.; Xu, Pengqi; Calder, Lesley J.; Borg, Annabel; Roustan, Chloë; Martin, Stephen R.; Rosenthal, Peter B.; Skehel, John J.; Gamblin, Steven J. (5 February 2021). "Structure and binding properties of Pangolin-CoV spike glycoprotein inform the evolution of SARS-CoV-2". Nature Communications. 12 (1): 837. Bibcode:2021NatCo..12..837W. doi:10.1038/s41467-021-21006-9. eISSN 2041-1723. PMC 7864994. PMID 33547281.
  26. ^ Perlman, Stanley; Peiris, Malik (15 February 2023). "Coronavirus research: knowledge gaps and research priorities". Nature Reviews Microbiology. 21 (3): 125–126. doi:10.1038/s41579-022-00837-3. eISSN 1740-1534. ISSN 1740-1526. PMID 36792727. S2CID 256875846. It is almost certain that the virus originated in bats and crossed species to humans either directly or indirectly via intermediary hosts.
  27. ^ Keusch, Gerald T.; Amuasi, John H.; Anderson, Danielle E.; Daszak, Peter; Eckerle, Isabella; Field, Hume; Koopmans, Marion; Lam, Sai Kit; Das Neves, Carlos G.; Peiris, Malik; Perlman, Stanley; Wacharapluesadee, Supaporn; Yadana, Su; Saif, Linda (18 October 2022). "Pandemic origins and a One Health approach to preparedness and prevention: Solutions based on SARS-CoV-2 and other RNA viruses". Proceedings of the National Academy of Sciences. 119 (42): e2202871119. Bibcode:2022PNAS..11902871K. doi:10.1073/pnas.2202871119. ISSN 0027-8424. PMC 9586299. PMID 36215506. S2CID 252818019. The increasing scientific evidence concerning the origins of Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is most consistent with a zoonotic origin and a spillover pathway from wildlife to people via wildlife farming and the wildlife trade.
  28. ^ SARS-CoV-2 is widely believed to have an original reservoir in bats,[18][19][20] though there may have been an intermediate host (such as palm civets,[21][22] minks,[23][22] or pangolins[24][25]) before spillover into humans.[26][27]
  29. ^ Walsh, Michael G.; Wiethoelter, Anke; Haseeb, M. A. (2017-08-15). "The impact of human population pressure on flying fox niches and the potential consequences for Hendra virus spillover". Scientific Reports. 7 (1): 8226. Bibcode:2017NatSR...7.8226W. doi:10.1038/s41598-017-08065-z. ISSN 2045-2322. PMC 5557840. PMID 28811483.
  30. ^ a b Becker, Daniel J.; Eby, Peggy; Madden, Wyatt; Peel, Alison J.; Plowright, Raina K. (January 2023). Ostfeld, Richard (ed.). "Ecological conditions predict the intensity of Hendra virus excretion over space and time from bat reservoir hosts". Ecology Letters. 26 (1): 23–36. Bibcode:2023EcolL..26...23B. doi:10.1111/ele.14007. ISSN 1461-023X. PMID 36310377.
  31. ^ Louten, Jennifer (2016), "Virus Replication", Essential Human Virology, Elsevier: 49–70, doi:10.1016/b978-0-12-800947-5.00004-1, ISBN 978-0-12-800947-5, PMC 7149683
[edit]