Title: Spillover and pandemic properties of zoonotic viruses with high host plasticity Christine Kreuder Johnson1, Peta L. Hitchens1, Tierra Smiley Evans1, Tracey Goldstein1, Kate Thomas1, Andrew Clements2, Damien O


, 1711–21 (2004). 268. Song, J. W. et al. Genetic diversity of Apodemus agrarius-borne Hantaan virus in Korea. Virus Genes 21



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190, 1711–21 (2004).

268. Song, J. W. et al. Genetic diversity of Apodemus agrarius-borne Hantaan virus in Korea. Virus Genes 21, 227–32 (2000).

269. Chua, K. B. et al. Tioman virus, a novel Paramyxovirus isolated from fruit bats in Malaysia. Virology 283, 215–29 (2001).

270. Playford, E. G. et al. Human Hendra virus encephalitis associated with equine outbreak, Australia, 2008. Emerg. Infect. Dis. 16, 219–223 (2010).

271. Field, H. Hendra virus outbreak with novel clinical features, Australia. Emerg. Infect. Dis. 16, 2008–2010 (2010).

272. Field, H. Hendra virus infection risks. Curr. Top. Microbiol. Immunol. 14, 77 – 78 (2009).

273. Wong, K. T. et al. Human Hendra virus infection causes acute and relapsing encephalitis. Neuropathol. Appl. Neurobiol. 35, 296–305 (2009).

274. Plowright, R. K. et al. Reproduction and nutritional stress are risk factors for Hendra virus infection in Little red flying foxes (Pteropus scapulatus). Proc. Biol. Sci. 275, 861–9 (2008).

275. Field, H. E. et al. Epidemiological perspectives on Hendra virus infection in horses and flying foxes. Aust. Vet. J. 85, 268–70 (2007).

276. Barker, S. The Australian paralysis tick may be the missing link in the transmission of Hendra virus from bats to horses to humans. Med. Hypotheses 60, 481–483 (2003).

277. Hayman, D. T. S. et al. Evidence of Henipavirus infection in West African fruit bats. PLoS One 3, e2739 (2008).

278. Breed, A. C., Field, H. E., Smith, C. S., Edmonston, J. & Meers, J. Bats without borders: long-distance movements and implications for disease risk management. Ecohealth 7, 204–12 (2010).

279. Chong, H. T., Abdullah, S. & Tan, C. T. Nipah virus and bats. Neurol. Asia 14, 73–76 (2009).

280. Pavio, N., Meng, X.-J. & Renou, C. Zoonotic Hepatitis E: animal reservoirs and emerging risks. Vet. Res. 41, 46 (2010).

281. Kaba, M., Davoust, B., Marié, J.-L. & Colson, P. Detection of Hepatitis E virus in wild boar (Sus scrofa) livers. Vet. J. 186, 259–61 (2010).

282. Kaba, M. et al. Hepatitis E virus infection in sheltered homeless persons, France. Emerg. Infect. Dis. 16, 1761–1764 (2010).

283. Meng, X. J. Hepatitis E virus: animal reservoirs and zoonotic risk. Vet. Microbiol. 140, 256–65 (2010).

284. Reuter, G., Fodor, D., Forgách, P., Kátai, A. & Szucs, G. Characterization and zoonotic potential of endemic Hepatitis E virus (HEV) strains in humans and animals in Hungary. J. Clin. Virol. 44, 277–81 (2009).

285. Takahashi, K., Kitajima, N., Abe, N. & Mishiro, S. Complete or near-complete nucleotide sequences of hepatitis E virus genome recovered from a wild boar, a deer, and four patients who ate the deer. Virology 330, 501–5 (2004).

286. Chang, Y. et al. Zoonotic risk of Hepatitis E virus (HEV): A study of HEV infection in animals and humans in suburbs of Beijing. Hepatol. Res. 39, 1153–8 (2009).

287. Worm, H. C., van der Poel, W. H. M. & Brandstätter, G. Hepatitis E: an overview. Microbes Infect. 4, 657–66 (2002).

288. Elmore, D. & Eberle, R. Monkey B virus (Cercopithecine Herpesvirus 1). Comp. Med. 58, 11–21 (2008).

289. Ritz, N., Curtis, N., Buttery, J. & Babl, F. E. Monkey bites in travelers: should we think of Herpes B virus? Pediatr. Emerg. Care 25, 529–31 (2009).

290. Huff, J. L. & Berry, P. A. B-virus (Cercopithecine Herpesvirus 1) infection in humans and macaques: potential for zoonotic disease. Emerg. Infect. Dis. 9, 246–250 (2003).

291. Jainkittivong, A. & Langlais, R. P. Herpes B virus infection. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 85, 399–403 (1998).

292. Espana, C. Herpesvirus simiae infection in Macaca radiata. Am. J. Phys. Anthr. 38, 447–454 (2005).

293. Jensen, K., Alvarado-ramy, F., González-martínez, J., Kraiselburd, E. & Rullán, J. B-virus and free-ranging macaques Puerto Rico. Emerg. Infect. Dis. 10, 494–496 (2004).

294. Lee, F., Lin, Y.-J., Deng, M.-C., Lee, T.-Y. & Huang, C.-C. Prevalence of antibody reaction with Cercopithecine Herpesvirus 1 antigen in Macaca cyclopis Macaca fascicularis, and Papio anubis in Taiwan. J. Med. Primatol. 36, 343–7 (2007).

295. Wilson, R. B., Holscher, M. a., Chang, T. & Hodges, J. R. Fatal Herpesvirus Simiae (B Virus) infection in a Patas monkey (Erythrocebus Patas). J. Vet. Diagnostic Investig. 2, 242–244 (1990).

296. Andrade, M. R. et al. Prevalence of antibodies to selected viruses in a long-term closed breeding colony of Rhesus macaques (Macaca mulatta) in Brazil. Am. J. Primatol. 59, 123–8 (2003).

297. Coulibaly, C. et al. A natural asymptomatic herpes B virus infection in a colony of laboratory brown capuchin monkeys (Cebus apella). Lab. Anim. 38, 432–438 (2004).

298. Engel, G. & Jones-Engel, L. Human exposure to Herpesvirus B–seropositive macaques, Bali, Indonesia. Emerg. Infect. Dis. 8, 789–795 (2002).

299. Jones-Engel, L. et al. Temple monkeys and health implications of commensalism, Kathmandu, Nepal. Emerg. Infect. Dis. 12, 900–906 (2006).

300. Johnson, B. W. et al. Ilheus virus isolate from a human, Ecuador. Emerg. Infect. Dis. 13, 956–8 (2007).

301. Anderson, C. R., Trinidad, T., Aitken, T. H. G., Downs, W. G. & Indies, W. The isolation of Ilheus virus from wild caught forest mosquitoes in Trinidad. Unknon...need to find 621–625 (1947).

302. Li, Y. et al. Persistent circulation of highly pathogenic influenza H5N1virus in Lake Qinghai Area of China. Avian Dis. 54, 821–829 (2010).

303. Desvaux, S. et al. Highly pathogenic Avian influenza virus (H5N1) outbreak in captive wild birds and cats, Cambodia. Emerg. Infect. Dis. 15, 475–479 (2009).

304. Roberton, S. I. et al. Avian influenza H5N1 in viverrids: implications for wildlife health and conservation. Proc. Biol. Sci. 273, 1729–32 (2006).

305. Yee, K. S., Carpenter, T. E. & Cardona, C. J. Epidemiology of H5N1 Avian influenza. Comp. Immunol. Microbiol. Infect. Dis. 32, 325–40 (2009).

306. Kayali, G., Ortiz, E. J., Chorazy, M. L. & Gray, G. C. Evidence of previous avian influenza infection among US turkey workers. Zoonoses Public Health 57, 265–72 (2010).

307. Keawcharoen, J. et al. Avian influenza H5N1 in tigers and leopards. Emerg. Infect. Dis. 10, 2189–91 (2004).

308. Stoops, A. C. et al. H5N1 surveillance in migratory birds in Java, Indonesia. Vector borne zoonotic Dis. 9, 695–702 (2009).

309. Yamamoto, Y., Nakamura, K., Yamada, M. & Ito, T. Zoonotic risk for influenza A (H5N1) infection in wild swan feathers. J. Vet. Med. Sci. 71, 1549–51 (2009).

310. Blanc, A. et al. Serologic evidence of influenza A and B viruses in South American fur seals (Arctocephalus australis). J. Wildl. Dis. 45, 519–21 (2009).

311. Osterhaus, a. D., Rimmelzwaan, G. F., Martina, B. E. E., Bestebroer, T. M. & Fouchier, R. A. M. Influenza B virus in seals. Science 288, 1051–1053 (2000).

312. Putkuri, N., Vaheri, A. & Vapalahti, O. Prevalence and protein specificity of human antibodies to Inkoo virus infection. Clin. Vaccine Immunol. 14, 1555–62 (2007).

313. Mayo, D. et al. Jamestown Canyon Virus: seroprevalence in Connecticut. Emerg. Infect. Dis. 7, 8–9 (2001).

314. Murdock, C. C., Olival, K. J. & Perkins, S. L. Molecular identification of host feeding patterns of snow-melt mosquitoes (Diptera: Culicidae): potential implications for the transmission ecology of Jamestown Canyon virus. J. Med. Entomol. 47, 226–229 (2010).

315. Zheng, H. et al. Jamestown Canyon virus detection in human tissue specimens. J. Clin. Pathol. 60, 787–93 (2007).

316. Nelson, D. M. et al. Prevalence of antibodies against Saint Louis encephalitis and Jamestown Canyon viruses in California horses. Comp. Immunol. Microbiol. Infect. Dis. 27, 209–15 (2004).

317. Sahu, S. P. et al. Isolation of Jamestown Canyon virus (California virus group) from vesicular lesions of a horse. J. Vet. Diagnostic Investig. 12, 80–83 (2000).

318. Andreadis, T. G., Anderson, J. F., Armstrong, P. M. & Main, A. J. Isolations of Jamestown canyon virus (Bunyaviridae: Orthobunyavirus) from field collected mosquitoes (Diptera: culicidaw) in connectivcut USA: A ten-year analysis. Vector-borne zoonotic Dis. 8, 175–188 (2008).

319. Armstrong, P. M. & Andreadis, T. G. Genetic relationships of Jamestown Canyon virus strains infecting mosquitoes collected in Connecticut. Am. J. Trop. Med. Hyg. 77, 1157–62 (2007).

320. Grimstad, P. R., Schmitt, S. M. & Williams, D. G. Prevalence of neutralizing antibody to Jamestown Canyon virus (California group) in populations of elk and moose in northern Michigan and Ontario, Canada. J. Wildl. Dis. 22, 453–458 (1986).

321. Grieve, S. Japanese encephalitis. Pract. Nurs. 21, (2010).

322. Nga, P. T. Shift in Japanese encephalitis virus (JEV) genotype circulating in northern Vietnam: implications for frequent introductions of JEV from Southeast Asia to East Asia. J. Gen. Virol. 85, 1625–1631 (2004).

323. Nitatpattana, N. et al. Change in Japanese encephalitis virus distribution, Thailand. Emerg. Infect. Dis. 14, 1762–5 (2008).

324. Erlanger, T. E., Weiss, S., Keiser, J., Utzinger, J. & Wiedenmayer, K. Past, present, and future of Japanese encephalitis. Emerg. Infect. Dis. 15, (2009).

325. Singha, H. et al. Complete genome sequence analysis of Japanese encephalitis virus isolated from a horse in India. Arch. Virol. 158, 113–22 (2013).

326. Lindahl, J. F. et al. Circulation of Japanese encephalitis virus in pigs and mosquito vectors within Can Tho city, Vietnam. PLoS Negl. Trop. Dis. 7, (2013).

327. Charrel, R. N. & de Lamballerie, X. Zoonotic aspects of Arenavirus infections. Vet. Microbiol. 140, 213–20 (2010).

328. Weaver, S. C. et al. Extreme genetic diversity among Pirital virus (Arenaviridae) isolates from western Venezuela. Virology 285, 110–8 (2001).

329. Cajimat, M. N. B. et al. Diversity among Tacaribe serocomplex viruses (family Arenaviridae) naturally associated with the Mexican woodrat (Neotoma mexicana). Virus Res. 133, 211–7 (2008).

330. Arata, A. A. & Gratz, N. G. The structure of rodent faunas associated with arenaviral infections. Bull. World Health Organ. 52, 621 (1975).

331. Enria, D., Briggiler, A. & Feuillade, M. An overview of the epidemiological, ecological and preventive hallmarks of Argentine haemorrhagic fever (Junin virus). Bull. Inst. Pasteur 96, 103–114 (1998).

332. Mills, J., Ellis, B. & Jr, K. M. Junin virus activity in rodents from endemic and nonendemic loci in central Argentina. Am. J. Trop. Med. Hyg. 44, 589–597 (1991).

333. Polop, J. et al. Spatial variation in abundance of the junin virus hosts in endemic and nonendemic Argentine haemorrhagic fever zones. Austral Ecol. 32, 245–253 (2007).

334. Chiappero, M. B., Gardenal, C. N. & Panzetta-Dutari, G. M. Isolation and characterization of microsatellite markers in Calomys musculinus (Muridae, Sigmodontinae, Phyllotini), the natural reservoir of Junin virus. Mol. Ecol. Notes 5, 593–595 (2005).

335. García, J. B. et al. Genetic diversity of the Junin virus in Argentina: geographic and temporal patterns. Virology 272, 127–36 (2000).

336. Polop, F. et al. On the relationship between the environmental history and the epidemiological situation of Argentine hemorrhagic fever. Ecol. Res. 23, 217–225 (2008).

337. Oliveira, R. C. et al. Genetic characterization of a Juquitiba-like viral lineage in Oligoryzomys nigripes in Rio de Janeiro, Brazil. Acta Trop. 112, 212–8 (2009).

338. Delfraro, A. et al. Juquitiba-like Hantavirus from 2 nonrelated rodent species, Uruguay. Emerg. Infect. Dis. 14, 1447–1451 (2008).

339. Calisher, C. H., Oro, J. B., Lord, R. D., Sabattini, M. S. & Karabatsos, N. Kairi virus identified from a fabrile horse in Argentina. Am. J. Trop. Med. Hyg. 39, 519–521 (1988).

340. Soto, V. et al. Complete nucleotide sequences of the small and medium RNA genome segments of Kairi virus (family Bunyaviridae). Arch. Virol. 154, 1555–8 (2009).

341. Mehla, R. et al. Recent ancestry of Kyasanur Forest disease virus. Emerg. Infect. Dis. 15, 1431–7 (2009).

342. Wang, J. Isolation of Kyasanur Forest disease virus from febrile patient, Yunnan, China. Emerg. Infect. Dis. 15, 326–328 (2009).

343. Pattnaik, P. Kyasanur Forest disease: an epidemiological view in India. Rev. Med. Virol. 16, 151–65 (2006).

344. Armstrong, P. M. & Andreadis, T. G. A new genetic variant of La Crosse virus (Bunyaviridae) isolated from New England. Am. J. Trop. Med. Hyg. 75, 491–6 (2006).

345. Borucki, M. K., Kempf, B. J., Blitvich, B. J., Blair, C. D. & Beaty, B. J. La Crosse virus: replication in vertebrate and invertebrate hosts. Microbes Infect. 4, 341–50 (2002).

346. Sokol, D. K., Kleiman, M. B. & Garg, B. P. La Crosse viral encephalitis mimics herpes simplex viral encephalitis. Pediatr. Neurol. 25, 413–5 (2001).

347. Rust, R. S., Thompson, W. H., Matthews, C. G., Beaty, B. J. & Chun, R. W. M. Topical review: La Crosse and other forms of California encephalitis. J. Child Neurol. 14, 1–14 (1999).

348. Balfour, H. H., Edelman, C. K., Bauer, H. & Siem, R. A. California arbovirus (La Crosse) infections. III. Epidemiology of California encephalitis in Minnesota. J. Infect. Dis. 133, 293–301 (1976).

349. Gerhardt, R. R. et al. First isolation of La Crosse virus from naturally infected Aedes albopictus. Emerg. Infect. Dis. 7, 807–811 (2001).

350. Haddow, A. D. & Odoi, A. The incidence risk, clustering, and clinical presentation of La Crosse virus infections in the eastern United States, 2003-2007. PLoS One 4, e6145 (2009).

351. Lambert, A. J. et al. La Crosse virus in Aedes albopictus mosquitoes, Texas, USA, 2009. Emerg. Infect. Dis. 16, 856–8 (2010).

352. Polop, F. J. et al. Temporal and spatial host abundance and prevalence of Andes Hantavirus in southern Argentina. Ecohealth 7, 176–84 (2010).

353. Carroll, D. S. et al. Hantavirus pulmonary syndrome in Central Bolivia: relationships between reservoir hosts, habitats, and viral genotypes. Am. J. Trop. Med. Hyg. 72, 42–6 (2005).

354. Levis, S. et al. Hantavirus pulmonary syndrome in northwestern Argentina: circulation of Laguna Negra virus associated with Calomys callosus. Am. J. Trop. Med. Hyg. 71, 658–63 (2004).

355. Yahnke, C. J., Meserve, P. L., Ksiazek, T. G. & Mills, J. N. Patterns of infection with Laguna Negra virus in wild populations of Calomys laucha in the central Paraguayan chaco. Am. J. Trop. Med. Hyg. 65, 768–76 (2001).

356. Raboni, S. M. et al. Evidence of circulation of Laguna Negra-like Hantavirus in the central west of Brazil: case report. J. Clin. Virol. 45, 153–6 (2009).

357. Ferrer, J. F. et al. Hantavirus infection in people inhabiting a highly endemic region of the Gran Chaco territory, Paraguay: association with Trypanosoma cruzi infection, epidemiological features and haematological characteristics. Ann. Trop. Med. Parasitol. 97, 269–80 (2003).

358. Padula, P. J. et al. Genetic diversity, distribution, and serological features of Hantavirus infection in five countries in South America. J. Clin. Microbiol. 38, 3029–35 (2000).

359. Cross, H., Province, N. E. & Ecija, N. Isolation of Getah virus from Nueva Ecija Province, Republic of the Philippines. Trans. R. Soc. Trop. Med. Hyg. 75, 312–313 (1981).

360. Safronetz, D. et al. Detection of Lassa virus, Mali. Emerg. Infect. Dis. 16, 1123–1127 (2010).

361. Emmerich, P., Günther, S. & Schmitz, H. Strain-specific antibody response to Lassa virus in the local population of west Africa. J. Clin. Virol. 42, 40–44 (2008).

362. Mcconnell, R. et al. Imported Lassa Fever, Pennsylvania, USA, 2010. Emerg. Infect. Dis. 16, 1598–1601 (2010).

363. Cooke, F. J. & Shapiro, D. S. ProMED update - Lassa fever case imported to Germany from Sierra Leone. Int. J. Infect. Dis. 10, 341–342 (2006).

364. Macher, A. M. & Wolfe, M. S. Historical Lassa Fever reports and 30-year clinical update. Emerg. Infect. Dis. 12, 835–837 (2006).

365. Omilabu, S. A. et al. Lassa fever, Nigeria, 2003 and 2004. Emerg. Infect. Dis. 11, 1642–4 (2005).

366. Chakarala, A. Imported Lassa Fever-New Jersey, 2004. J. Am. Med. Assoc. 292, 2828–2830 (2004).

367. Crowcroft, N. S. et al. The public health response to a case of Lassa fever in London in 2000. J. Infect. 48, 221–8 (2004).

368. Meulen, J. Ter et al. Short Communication: Lassa fever in Sierra Leone UN peacekeepers are at risk. Trop. Med. Int. Heal. 6, 83–84 (2001).

369. Garcia, F. L. B. et al. A retrospective laboratory analysis of clinically diagnosed Lassa Fever cases in a tertiary hospital in Nigeria. Int. J. Infect. Dis. 14, e209–e209 (2010).

370. Okogbenin, S. A. et al. Prevalence and presentation of Lassa fever in Nigerian children. Int. J. Infect. Dis. 14, e380–e380 (2010).

371. Ehichioya, D. U. et al. Lassa Fever, Nigeria, 2005-2008. Emerg. Infect. Dis. 16, 1040–1042 (2010).

372. Kernéis, S. et al. Prevalence and risk factors of Lassa seropositivity in inhabitants of the forest region of Guinea: a cross-sectional study. PLoS Negl. Trop. Dis. 3, e548 (2009).

373. Ehichioya1, D. U., Omilabu, S., Asogun, D. A., Hass, M. & Gunther, S. Clinical and serological evidence of Lassa Fever in Edo State, Nigeria. Int. J. Infect. Dis. 12, e331–e332 (2008).

374. Fair, J. et al. Lassa virus-infected rodents in refugee camps in Guinea: a looming threat to public health in a politically unstable region. Vector Borne Zoonotic Dis. 7, 167–71 (2007).

375. Lecompte, E. et al. Mastomys natalensis and Lassa fever, West Africa. Emerg. Infect. Dis. 12, 1971–4 (2006).

376. Niklasson, B. et al. A new Picornavirus isolated from bank voles (Clethrionomys glareolus). Virology 255, 86–93 (1999).

377. Niklasson, B., Almqvist, P. R., Hörnfeldt, B. & Klitz, W. Sudden infant death syndrome and Ljungan virus. Forensic Sci. Med. Pathol. 5, 274–9 (2009).

378. Hauffe, H. C. et al. Ljungan virus detected in bank voles (Myodes glareolus) and yellow-necked mice (Apodemus flavicollis) from Northern Italy. J. Wildl. Dis. 46, 262–6 (2010).

379. Donoso Mantke, O., Kallies, R., Niklasson, B., Nitsche, A. & Niedrig, M. A new quantitative real-time reverse transcriptase PCR assay and melting curve analysis for detection and genotyping of Ljungan virus strains. J. Virol. Methods 141, 71–7 (2007).

380. Briese, T. et al. Genetic detection and characterization of Lujo virus, a new hemorrhagic fever-associated arenavirus from southern Africa. PLoS Pathog. 5, e1000455 (2009).

381. Paweska, J. T. et al. Nosocomial outbreak of novel arenavirus infection, southern Africa. Emerg. Infect. Dis. 15, 1598–602 (2009).

382. Rousseau, M., Saron, M., Brouqui, P. & Bourgeade, A. Lymphocytic choriomeningitis virus in southern France: four case reports and a review of the literature. Eur. J. Epidemiol. 13, 817–823 (1997).

383. Karamany, R. El & Imam, I. Antibodies to Lymphocytic choriomeningitis virus in wild rodent sera in Egypt. J. Hyg. Epidemiol. Microbiol. Immunol. 35, 97–103 (1991).

384. Morita, C., Matsuura, Y. & Fujii, H. Isolation of Lymphocytic choriomeningitis virus from wild house mice (Mus musculus) in Osaka Port, Japan. J. Vet. Med. Sci. 53, 889–892 (1991).

385. Becker, S., Bennett, M., Stewart, J. & Hurst, J. Serological survey of virus infection among wild house mice (Mus domesticus) in the UK. Lab. Anim. 41, 229–238 (2007).

386. Ledesma, J. et al. Independent lineage of Lymphocytic choriomeningitis virus in wood mice (Apodemus sylvaticus), Spain. Emerg. Infect. Dis. 15, 1677–1680 (2009).

387. Tagliapietra, V. et al. Spatial and temporal dynamics of Lymphocytic choriomeningitis virus in wild rodents, northern Italy. Emerg. Infect. Dis. 15, 1019–1025 (2009).

388. Marrie, T. & Saron, M. Seroprevalence of Lymphocytic choriomeningitis virus in Nova Scotia. Am. J. Trop. Med. Hyg. 58, 47–49 (1998).

389. Sottosanti, J. et al. Serological study of the Lymphocytic choriomeningitis virus (LCMV) in an inner city of Argentina. J. Med. Virol. 76, 285–289 (2005).

390. Asnis, D. S., Muana, O., Kim, D. G., Garcia, M. & Rollin, P. E. Lymphocytic choriomeningitis virus meningitis, New York, NY, USA, 2009. Emerg. Infect. Dis. 16, 328–331 (2010).

391. Asper, M. et al. First outbreak of Callitrichid Hepatitis in Germany : genetic characterization of the causative Lymphocytic choriomeningitis virus strains. Virology 284, 203–213 (2001).

392. Ceianu, C. et al. Letter to the Editor - Lymphocytic choriomeningitis in a pet store worker in Romania. Clinial Vaccine Immunol. 15, 1749 (2008).

393. Johnson, K. Epidemiology of Machupo virus infection. III. Significance of virological observations in man and animals. Am. J. Trop. Med. Hyg. 14, 816–8 (1965).

394. Murphy, F. Arenavirus taxonomy: a review. Bull. World Health Organ. 52, 387–391 (1975).

395. Report, W. Ebola haemorrhagic fever in Sudan , 1976. Bull. World Health Organ. 56, (1978).

396. Pourrut, X. et al. Large serological survey showing cocirculation of Ebola and Marburg viruses in Gabonese bat populations, and a high seroprevalence of both viruses in Rousettus aegyptiacus. BMC Infect. Dis. 9, 159 (2009).

397. Lahm, S., Kombila, M., Swanepoel, R. & Barnes, R. F. W. Morbidity and mortality of wild animals in relation to outbreaks of Ebola haemorrhagic fever in Gabon, 1994-2003. Trans. R. Soc. Trop. Med. Hyg. 101, 64–78 (2007).

398. Towner, J. S. et al. Isolation of genetically diverse Marburg viruses from Egyptian fruit bats. PLoS Pathog. 5, e1000536 (2009).

399. Timen, A. et al. Response to imported case of Marburg Hemorrhagic Fever, the Netherlands. Emerg. Infect. Dis.


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