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A Human Lung Xenograft Mouse Model of Nipah Virus Infection
Nipah virus (NiV) is a highly pathogenic zoonotic virus that causes fatal disease in humans and a variety of other mammalian hosts including pigs. Given the lack of effective therapeutics and vaccines, this virus is considered a public health and agricultural concern, and listed as category C priority pathogen for biodefense research by the National Institute of Allergy and Infectious Diseases. Both animal-to-human and human-to-human transmission has been observed. Studies on the molecular mechanisms of NiV-mediated pathogenesis have been hampered by the lack of biologically relevant in vivo models for studying the initial host responses to NiV infection in the human lung. We show here a new small animal model in which we transplant human lung tissue for studying the pathogenesis of NiV. We showed that NiV can replicate to high levels in the human lung. NiV causes extensive damage to the lung tissue and induces important regulators of the inflammatory response. This study is the first to use a human lung transplant for studying infectious diseases, a powerful model for studying the pathogenesis of NiV infection, and will open up new possibilities for studying virus-host interactions.
Vyšlo v časopise: A Human Lung Xenograft Mouse Model of Nipah Virus Infection. PLoS Pathog 10(4): e32767. doi:10.1371/journal.ppat.1004063
Kategorie: Research Article
prolekare.web.journal.doi_sk: https://doi.org/10.1371/journal.ppat.1004063Souhrn
Nipah virus (NiV) is a highly pathogenic zoonotic virus that causes fatal disease in humans and a variety of other mammalian hosts including pigs. Given the lack of effective therapeutics and vaccines, this virus is considered a public health and agricultural concern, and listed as category C priority pathogen for biodefense research by the National Institute of Allergy and Infectious Diseases. Both animal-to-human and human-to-human transmission has been observed. Studies on the molecular mechanisms of NiV-mediated pathogenesis have been hampered by the lack of biologically relevant in vivo models for studying the initial host responses to NiV infection in the human lung. We show here a new small animal model in which we transplant human lung tissue for studying the pathogenesis of NiV. We showed that NiV can replicate to high levels in the human lung. NiV causes extensive damage to the lung tissue and induces important regulators of the inflammatory response. This study is the first to use a human lung transplant for studying infectious diseases, a powerful model for studying the pathogenesis of NiV infection, and will open up new possibilities for studying virus-host interactions.
Zdroje
1. RockxB, WinegarR, FreibergAN (2012) Recent progress in henipavirus research: molecular biology, genetic diversity, animal models. Antiviral Res 95 : 135–149.
2. ChuaKB, GohKJ, WongKT, KamarulzamanA, TanPS, et al. (1999) Fatal encephalitis due to Nipah virus among pig-farmers in Malaysia. Lancet 354 : 1257–1259.
3. PatonNI, LeoYS, ZakiSR, AuchusAP, LeeKE, et al. (1999) Outbreak of Nipah-virus infection among abattoir workers in Singapore. Lancet 354 : 1253–1256.
4. HsuVP, HossainMJ, ParasharUD, AliMM, KsiazekTG, et al. (2004) Nipah virus encephalitis reemergence, Bangladesh. Emerg Infect Dis 10 : 2082–2087.
5. GurleyES, MontgomeryJM, HossainMJ, BellM, AzadAK, et al. (2007) Person-to-person transmission of Nipah virus in a Bangladeshi community. Emerg Infect Dis 13 : 1031–1037.
6. HossainMJ, GurleyES, MontgomeryJM, BellM, CarrollDS, et al. (2008) Clinical presentation of nipah virus infection in Bangladesh. Clin Infect Dis 46 : 977–984.
7. EscaffreO, BorisevichV, RockxB (2013) Pathogenesis of Hendra and Nipah virus infection in humans. J Infect Dev Ctries 7 : 308–311.
8. WongKT, ShiehW-J, KumarS, NorainK, AbdullahW, et al. (2002) Nipah Virus Infection: Pathology and Pathogenesis of an Emerging Paramyxoviral Zoonosis. The American journal of pathology 161 : 2153–2167.
9. LoMK, MillerD, AljofanM, MungallBA, RollinPE, et al. (2010) Characterization of the antiviral and inflammatory responses against Nipah virus in endothelial cells and neurons. Virology 404 : 78–88.
10. ErbarS, DiederichS, MaisnerA (2008) Selective receptor expression restricts Nipah virus infection of endothelial cells. Virol J 5 : 142.
11. MaisnerA, NeufeldJ, WeingartlH (2009) Organ - and endotheliotropism of Nipah virus infections in vivo and in vitro. Thromb Haemost 102 : 1014–1023.
12. EscaffreO, BorisevichV, CarmicalJR, PrusakD, PrescottJ, et al. (2013) Henipavirus Pathogenesis in Human Respiratory Epithelial Cells. J Virol 87(6): 3284–94.
13. RockxB, BriningD, KramerJ, CallisonJ, EbiharaH, et al. (2011) Clinical outcome of henipavirus infection in hamsters is determined by the route and dose of infection. J Virol 85 : 7658–7671.
14. BossartKN, RockxB, FeldmannF, BriningD, ScottD, et al. (2012) A Hendra virus G glycoprotein subunit vaccine protects African green monkeys from Nipah virus challenge. Sci Transl Med 4 : 146ra107.
15. BossartKN, ZhuZ, MiddletonD, KlippelJ, CrameriG, et al. (2009) A neutralizing human monoclonal antibody protects against lethal disease in a new ferret model of acute nipah virus infection. PLoS Pathog 5: e1000642.
16. GeisbertTW, Daddario-DicaprioKM, HickeyAC, SmithMA, ChanYP, et al. (2010) Development of an acute and highly pathogenic nonhuman primate model of nipah virus infection. PLoS One 5: e10690.
17. WongKT, GrosjeanI, BrissonC, BlanquierB, Fevre-MontangeM, et al. (2003) A golden hamster model for human acute Nipah virus infection. Am J Pathol 163 : 2127–2137.
18. PodestaJE, Al-JamalKT, HerreroMA, TianB, Ali-BoucettaH, et al. (2009) Antitumor activity and prolonged survival by carbon-nanotube-mediated therapeutic siRNA silencing in a human lung xenograft model. Small 5 : 1176–1185.
19. SavidgeTC, MoreyAL, FergusonDJ, FlemingKA, ShmakovAN, et al. (1995) Human intestinal development in a severe-combined immunodeficient xenograft model. Differentiation 58 : 361–371.
20. SavidgeTC, PanWH, NewmanP, O'BrienM, AntonPM, et al. (2003) Clostridium difficile toxin B is an inflammatory enterotoxin in human intestine. Gastroenterology 125 : 413–420.
21. KollmannTR, Pettoello-MantovaniM, KatopodisNF, HachamovitchM, RubinsteinA, et al. (1996) Inhibition of acute in vivo human immunodeficiency virus infection by human interleukin 10 treatment of SCID mice implanted with human fetal thymus and liver. Proc Natl Acad Sci U S A 93 : 3126–3131.
22. Abele-OhlS, LeisM, WollinM, MahmoudianS, HoffmannJ, et al. (2012) Human cytomegalovirus infection leads to elevated levels of transplant arteriosclerosis in a humanized mouse aortic xenograft model. Am J Transplant 12 : 1720–1729.
23. UhlenM, OksvoldP, FagerbergL, LundbergE, JonassonK, et al. (2010) Towards a knowledge-based Human Protein Atlas. Nat Biotechnol 28 : 1248–1250.
24. ShultzLD, SchweitzerPA, ChristiansonSW, GottB, SchweitzerIB, et al. (1995) Multiple defects in innate and adaptive immunologic function in NOD/LtSz-scid mice. J Immunol 154 : 180–191.
25. ClaytonBA, MiddletonD, BergfeldJ, HainingJ, ArkinstallR, et al. (2012) Transmission Routes for Nipah Virus from Malaysia and Bangladesh. Emerg Infect Dis 18 : 1983–1993.
26. DeBuysscherBL, de WitE, MunsterVJ, ScottD, FeldmannH, et al. (2013) Comparison of the pathogenicity of Nipah virus isolates from Bangladesh and Malaysia in the Syrian hamster. PLoS Negl Trop Dis 7: e2024.
27. MathieuC, PohlC, SzecsiJ, Trajkovic-BodennecS, DevergnasS, et al. (2011) Nipah virus uses leukocytes for efficient dissemination within a host. J Virol 85 : 7863–7871.
28. DhondtKP, MathieuC, ChalonsM, ReynaudJM, VallveA, et al. (2013) Type I interferon signaling protects mice from lethal henipavirus infection. J Infect Dis 207 : 142–151.
29. DupsJ, MiddletonD, YamadaM, MonaghanP, LongF, et al. (2012) A new model for Hendra virus encephalitis in the mouse. PLoS One 7: e40308.
30. RockxB, BaasT, ZornetzerGA, HaagmansB, SheahanT, et al. (2009) Early upregulation of acute respiratory distress syndrome-associated cytokines promotes lethal disease in an aged-mouse model of severe acute respiratory syndrome coronavirus infection. J Virol 83 : 7062–7074.
31. GaoR, BhatnagarJ, BlauDM, GreerP, RollinDC, et al. (2013) Cytokine and chemokine profiles in lung tissues from fatal cases of 2009 pandemic influenza A (H1N1): role of the host immune response in pathogenesis. Am J Pathol 183 : 1258–1268.
32. BaskinCR, Bielefeldt-OhmannH, TumpeyTM, SabourinPJ, LongJP, et al. (2009) Early and sustained innate immune response defines pathology and death in nonhuman primates infected by highly pathogenic influenza virus. Proc Natl Acad Sci U S A 106 : 3455–3460.
33. CameronMJ, Bermejo-MartinJF, DaneshA, MullerMP, KelvinDJ (2008) Human immunopathogenesis of severe acute respiratory syndrome (SARS). Virus Res 133 : 13–19.
34. MedfordAR, MillarAB (2006) Vascular endothelial growth factor (VEGF) in acute lung injury (ALI) and acute respiratory distress syndrome (ARDS): paradox or paradigm? Thorax 61 : 621–626.
35. CalderonVE, ValbuenaG, GoezY, JudyBM, HuanteMB, et al. (2013) A humanized mouse model of tuberculosis. PLoS One 8: e63331.
36. MeduriGU, HeadleyS, KohlerG, StentzF, TolleyE, et al. (1995) Persistent elevation of inflammatory cytokines predicts a poor outcome in ARDS. Plasma IL-1 beta and IL-6 levels are consistent and efficient predictors of outcome over time. Chest 107 : 1062–1073.
37. HeadleyAS, TolleyE, MeduriGU (1997) Infections and the inflammatory response in acute respiratory distress syndrome. Chest 111 : 1306–1321.
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Hygiena a epidemiológia Infekčné lekárstvo Laboratórium
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