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Spillover Infection
editSpillover 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
editSpillover 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 hydatido sis. 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
editCommercially 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]
Causes of Spillover
editZoonotic 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.[18] 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.[19] 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.[20] When the novel eukaryotic organism is not available for the virus to infect, it must jump to another host.[19] 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]
References
edit- ^ a b c d Plowright, Raina K.; Parrish, Colin R.; McCallum, Hamish; Hudson, Peter J.; Ko, Albert I.; Graham, Andrea L.; Lloyd-Smith, James O. (2017–18). "Pathways to zoonotic spillover". Nature Reviews Microbiology. 15 (8): 502–510. doi:10.1038/nrmicro.2017.45. ISSN 1740-1534.
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: CS1 maint: date format (link) - ^ Carlson, Colin J.; Albery, Gregory F.; Merow, Cory; Trisos, Christopher H.; Zipfel, Casey M.; Eskew, Evan A.; Olival, Kevin J.; Ross, Noam; Bansal, Shweta (28 April 2022). "Climate change increases cross-species viral transmission risk". Nature. 607 (7919): 555–562. Bibcode:2022Natur.607..555C. doi:10.1038/s41586-022-04788-w. ISSN 1476-4687. PMID 35483403. S2CID 248430532.
- ^ Power, AG; Mitchell, CE (Nov 2004). "Pathogen spillover in disease epidemics". The American Naturalist. 164 (Suppl 5): S79–89. doi:10.1086/424610. PMID 15540144. S2CID 16762851.
- ^ 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.
- ^ a b 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.
- ^ Aiewsakun, Pakorn; Katzourakis, Aris (2015-05-01). "Endogenous viruses: Connecting recent and ancient viral evolution". Virology. 60th Anniversary Issue. 479–480: 26–37. doi:10.1016/j.virol.2015.02.011. ISSN 0042-6822.
- ^ Ebola. (2014). National Center for Emerging and Zoonotic Infectious Diseases, Division of High-Consequence Pathogens and Pathology, Department of Health & Human Services, CDC.
- ^ Carlson, Colin J.; Albery, Gregory F.; Merow, Cory; Trisos, Christopher H.; Zipfel, Casey M.; Eskew, Evan A.; Olival, Kevin J.; Ross, Noam; Bansal, Shweta (28 April 2022). "Climate change increases cross-species viral transmission risk". Nature. 607 (7919): 555–562. Bibcode:2022Natur.607..555C. doi:10.1038/s41586-022-04788-w. ISSN 1476-4687. PMID 35483403. S2CID 248430532.
- ^ Rulli, Maria Cristina; Santini, Monia; Hayman, David T. S.; d'Odorico, Paolo (2017). "The nexus between forest fragmentation in Africa and Ebola virus disease outbreaks". Scientific Reports. 7: 41613. Bibcode:2017NatSR...741613R. doi:10.1038/srep41613. PMC 5307336. PMID 28195145.
- ^ a b 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. doi:10.1111/1365-2664.12134. S2CID 3937352.
- ^ 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. doi:10.1007/s10530-015-0859-6. ISSN 1387-3547.
- ^ 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.
- ^ 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.
- ^ 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.
- ^ 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.
- ^ Graystock, Peter; Blane, Edward J.; McFrederick, Quinn S.; Goulson, Dave; Hughes, William O. H. (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.
- ^ Carrington, Damian (18 July 2013). "Imported bumblebees pose risk to UK's wild and honeybee population – study". The Guardian.
- ^ 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. doi:10.1038/s41598-017-08065-z. ISSN 2045-2322.
- ^ a b Becker, Daniel J.; Eby, Peggy; Madden, Wyatt; Peel, Alison J.; Plowright, Raina K. (2023-01). 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. doi:10.1111/ele.14007. ISSN 1461-023X.
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(help) - ^ Louten, Jennifer (2016). "Virus Replication". Essential Human Virology: 49–70. doi:10.1016/B978-0-12-800947-5.00004-1. PMC 7149683.