Literature DB >> 16848051

Feral cats and risk for Nipah virus transmission.

Jonathan H Epstein, Sohayati Abdul Rahman, Jennifer A Zambriski, Kim Halpin, Greer Meehan, Abdul Aziz Jamaluddin, Sharifah Syed Hassan, Hume E Field, Alex D Hyatt, Peter Daszak.   

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Year:  2006        PMID: 16848051      PMCID: PMC3291044          DOI: 10.3201/eid1207.050799

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


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To the Editor: Nipah virus (NiV) emerged in peninsular Malaysia in 1998 and 1999 as a respiratory and neurologic disease of domestic pigs and an acute febrile encephalitic disease in humans (). Nipah virus infection is associated with a case-fatality ratio of 40% to 76% in humans (,). Cats (Felis catus) were infected with NiV at the site of the outbreak in northern Malaysia (). Experimental studies have shown that cats are susceptible to Hendra virus and NiV (,). Infected cats shed NiV through the nasopharynx and in urine while viremic, and 1 (of 2) recovered from experimental NiV infection with a high neutralizing antibody titer (>256) within 21 days (). Fruit bats of the genus Pteropus are believed to be the reservoir for NiV in Malaysia (). In June 2000, NiV was isolated from partially eaten fruit and from the urine of Pteropus hypomelanus in the village of Air Batang on Tioman Island, Peninsular Malaysia (). Although humans live in close proximity to these bats, no evidence for local human exposure to NiV has been seen (). In contrast, epidemiologic evidence from recent NiV outbreaks in Bangladesh suggests that direct infection from pteropid bats may occur, possibly when bats are pregnant (,). Despite limited contact with bats, residents and visitors to Air Batang have ample opportunity for close contact with feral cats, which are often fed and sometimes housed by residents. Cats have been observed under trees that are occupied by roosting fruit bats in Air Batang. NiV could be transmitted from bats to cats through urine and then among cats oronasally, given their gregarious nature, which frequently includes mutual grooming. Cats are also frequently seen in close contact with humans in restaurants, on the tables, and in food preparation areas, where they are fed. If NiV is also present in bat fetal tissues, cats could become infected through contact with or by eating these tissues after mass births among bats. We tested feral cats from Air Batang for neutralizing antibodies to NiV to determine whether cats might play a role in the zoonotic transmission of Nipah virus. Fifty bats were captured from Air Batang and tested for NiV and neutralizing antibodies to NiV as part of a long-term NiV surveillance study (A. Rahman, unpub. data). Thirty-two cats were caught July 12–19, 2004, in a 200-m radius of a bat colony. Cats were anesthetized, and 3.0 mL blood was collected from the jugular vein or medial saphenous vein. Serum was allowed to separate at 4°C for 24 hours and was then further separated and frozen in liquid nitrogen. Serum was tested by serum neutralization test (SNT), which is considered the reference standard for serologic assays, at the Australian Animal Health Laboratory, Geelong, Australia, as described (,). The time of year was similar to the time when NiV was isolated from bats in 2000; however, none of the 32 cats (18 males, 14 females; 25 adults, 7 juveniles [<1 year of age]) had detectable antibodies to NiV on SNT. All cats appeared healthy except for 1 adult that was markedly jaundiced. The period of the study did not overlap the seasonal gestation period of P. hypomelanus, and none of the adult female bats tested (n = 20) were pregnant. Although attempts to isolate virus from bat urine and saliva were unsuccessful (A. Rahman, unpub. data), 7 (14%) of 50 bats, including 1 (8%) of 13 post-weaning juveniles (≈4 months to 2 years of age) had neutralizing antibodies (all >32) to NiV on SNT, which suggests that virus had circulated in the colony since 2000. Our finding of no seropositive cats may be explained in 3 ways: 1) feral cats are rarely, if at all, exposed to NiV in nature; 2) the death rate from NiV infection in cats is so high that few or none survive with immunity; or 3) our sample size was too small to detect a seropositive cat. We believe that the first hypothesis is most likely. A low incidence of NiV infection in this population of bats (95% confidence interval for 0 of 50 bats, 0.00–0.71), combined with a short viremic period, would make transmission between bats and cats unlikely. However, if transmission occurred, we would expect to find some cats with a detectable titer (). While the exact age of the cats in this survey was unknown, 25 (78%) of 32 were adults (>1 year of age) and may have been in Air Batang either in 2000, when NiV was isolated from bats, or during a more recent outbreak. We conclude that exposure of feral or peridomestic cats to Nipah virus on Tioman Island is rare and that the risk for zoonotic transmission is low.
  8 in total

1.  Isolation of Nipah virus from Malaysian Island flying-foxes.

Authors:  Kaw Bing Chua; Chong Lek Koh; Poh Sim Hooi; Kong Fatt Wee; Jenn Hui Khong; Beng Hooi Chua; Yee Peng Chan; Mou Eng Lim; Sai Kit Lam
Journal:  Microbes Infect       Date:  2002-02       Impact factor: 2.700

2.  Nipah virus: a recently emergent deadly paramyxovirus.

Authors:  K B Chua; W J Bellini; P A Rota; B H Harcourt; A Tamin; S K Lam; T G Ksiazek; P E Rollin; S R Zaki; W Shieh; C S Goldsmith; D J Gubler; J T Roehrig; B Eaton; A R Gould; J Olson; H Field; P Daniels; A E Ling; C J Peters; L J Anderson; B W Mahy
Journal:  Science       Date:  2000-05-26       Impact factor: 47.728

3.  Susceptibility of cats to equine morbillivirus.

Authors:  H A Westbury; P T Hooper; S L Brouwer; P W Selleck
Journal:  Aust Vet J       Date:  1996-08       Impact factor: 1.281

Review 4.  Nipah virus infection of pigs in peninsular Malaysia.

Authors:  M N Mohd Nor; C H Gan; B L Ong
Journal:  Rev Sci Tech       Date:  2000-04       Impact factor: 1.181

Review 5.  Laboratory diagnosis of Nipah and Hendra virus infections.

Authors:  P Daniels; T Ksiazek; B T Eaton
Journal:  Microbes Infect       Date:  2001-04       Impact factor: 2.700

6.  Experimental Nipah virus infection in pigs and cats.

Authors:  D J Middleton; H A Westbury; C J Morrissy; B M van der Heide; G M Russell; M A Braun; A D Hyatt
Journal:  J Comp Pathol       Date:  2002 Feb-Apr       Impact factor: 1.311

7.  Nipah virus encephalitis reemergence, Bangladesh.

Authors:  Vincent P Hsu; Mohammed Jahangir Hossain; Umesh D Parashar; Mohammed Monsur Ali; Thomas G Ksiazek; Ivan Kuzmin; Michael Niezgoda; Charles Rupprecht; Joseph Bresee; Robert F Breiman
Journal:  Emerg Infect Dis       Date:  2004-12       Impact factor: 6.883

8.  Nipah virus infection in bats (order Chiroptera) in peninsular Malaysia.

Authors:  J M Yob; H Field; A M Rashdi; C Morrissy; B van der Heide; P Rota; A bin Adzhar; J White; P Daniels; A Jamaluddin; T Ksiazek
Journal:  Emerg Infect Dis       Date:  2001 May-Jun       Impact factor: 6.883

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Review 1.  Changing resource landscapes and spillover of henipaviruses.

Authors:  Maureen K Kessler; Daniel J Becker; Alison J Peel; Nathan V Justice; Tamika Lunn; Daniel E Crowley; Devin N Jones; Peggy Eby; Cecilia A Sánchez; Raina K Plowright
Journal:  Ann N Y Acad Sci       Date:  2018-08-23       Impact factor: 5.691

Review 2.  Hendra and nipah infection: pathology, models and potential therapies.

Authors:  Frederic Vigant; Benhur Lee
Journal:  Infect Disord Drug Targets       Date:  2011-06

3.  Mutation of YMYL in the Nipah virus matrix protein abrogates budding and alters subcellular localization.

Authors:  Michael J Ciancanelli; Christopher F Basler
Journal:  J Virol       Date:  2006-09-27       Impact factor: 5.103

4.  Nipah virus sequesters inactive STAT1 in the nucleus via a P gene-encoded mechanism.

Authors:  Michael J Ciancanelli; Valentina A Volchkova; Megan L Shaw; Viktor E Volchkov; Christopher F Basler
Journal:  J Virol       Date:  2009-06-10       Impact factor: 5.103

5.  The nonstructural proteins of Nipah virus play a key role in pathogenicity in experimentally infected animals.

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Journal:  PLoS One       Date:  2010-09-15       Impact factor: 3.240

6.  Qualitative release assessment to estimate the likelihood of henipavirus entering the United Kingdom.

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Journal:  PLoS One       Date:  2012-02-06       Impact factor: 3.240

Review 7.  Henipavirus infections: lessons from animal models.

Authors:  Kévin P Dhondt; Branka Horvat
Journal:  Pathogens       Date:  2013-04-09

Review 8.  Screening and structure-based modeling of T-cell epitopes of Nipah virus proteome: an immunoinformatic approach for designing peptide-based vaccine.

Authors:  Mohit Kamthania; D K Sharma
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Review 9.  Molecular epidemiology and phylogeny of Nipah virus infection: A mini review.

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Journal:  Asian Pac J Trop Med       Date:  2016-05-31       Impact factor: 1.226

Review 10.  Envelope-receptor interactions in Nipah virus pathobiology.

Authors:  Benhur Lee
Journal:  Ann N Y Acad Sci       Date:  2007-04       Impact factor: 5.691

  10 in total

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