Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 8, Number 9—September 2002
Dispatch

Antibodies to Nipah-Like Virus in Bats (Pteropus lylei), Cambodia

Article Metrics
112
citations of this article
EID Journal Metrics on Scopus
Author affiliations: *United States Naval Medical Research Unit Number 2, Phnom Penh, Cambodia; †Centers for Disease Control and Prevention, Atlanta, Georgia, USA; ‡National Institute of Public Health, Ministry of Health, Phnom Penh, Cambodia; §Wildlife Conservation Society, Phnom Penh, Cambodia;

Cite This Article

Abstract

Serum specimens from fruit bats were obtained at restaurants in Cambodia. We detected antibodies cross-reactive to Nipah virus by enzyme immunoassay in 11 (11.5%) of 96 Lyle’s flying foxes (Pteropus lylei). Our study suggests that viruses closely related to Nipah or Hendra viruses are more widespread in Southeast Asia than previously documented.

A large outbreak of encephalitis among swine farmers in Malaysia occurred from October 1998 to April 1999. Initially, Japanese encephalitis virus (JEV), a mosquito-borne pathogen endemic to the region, was suspected as the causative agent. However, a new paramyxovirus, Nipah virus, which is closely related to Hendra virus (HeV), was later implicated as the cause. Unlike JEV, Nipah virus predominated in adults rather than children. Nipah virus cases clustered in members of the same household, suggesting a high attack rate; in contrast, JEV causes symptomatic encephalitis in approximately 1/300 infected persons. A high proportion of Nipah virus patients had direct contact with pigs, unlike others in the same neighborhood who did not have the virus (providing evidence against a mosquito-borne disease); in addition, many of the pigs belonging to affected farmers had an associated history of illness (15).

Clinically and epidemiologically, the Nipah virus cases in humans also differed from the few reported HeV infections (6). HeV is transmitted from horses, and two of three patients with HeV infections had severe respiratory involvement; only one patient had severe meningoencephalitis. In contrast, Nipah virus infections involved direct contact with pigs and predominant central nervous system disease, with only mild or undiagnosed clinical or radiologic evidence of pulmonary involvement. Incubation periods were <1 month. The main symptom was fever with headache, followed by rapid deterioration in consciousness (1,4).

Nipah virus infection in pigs was frequently asymptomatic or, alternatively, occurred as an acute febrile illness with temperatures >40°C, accompanied by signs of respiratory and neurologic disease. Respiratory signs included open-mouth breathing, increased or forced respiration, and a harsh, nonproductive cough. Neurologic signs included head pressing, agitation and biting at bars, tetanic spasms, trembling, and muscle fasciculations (7,8).

Comprehensive studies of domestic animals and wildlife showed that a substantial proportion of Malaysian fruit bats (genus Pteropus) had neutralizing antibodies to Nipah virus (7,9). Nipah virus was recently isolated from urine of Malaysian small flying foxes (Pt. hypomelanus) (10). HeV was detected in the four Pteropus spp. that occur in Australia, with a moderate (20%–25%) prevalence of HeV-neutralizing antibody (11). In addition, HeV was isolated from the grey-headed flying fox (Pt. poliocephalus) and black flying fox (Pt. lecto) (12). In preliminary studies in Indonesia, antibodies to Nipah-like viruses have been detected in other Pteropus spp. (T. Ksiazek, pers. comm.).

The Study

To further investigate the distribution of this new group of viruses, we investigated the prevalence of virus antibodies in other members of the genus Pteropus in Cambodia. In restaurants where bats are eaten in Phnom Penh, we collected 2-mL blood specimens from each bat as it was prepared for food. The restaurant owners purchased bats from a hunter who trapped them in Kampong Cham Province and transported them alive to restaurants in Phnom Penh. We stored the whole blood on wet ice for as long as 48 h, then transported it to the U.S. Naval Medical Research Unit No. 2, National Institute of Public Health Laboratory, in Phnom Penh on wet ice, and centrifuged it to separate the serum from the clot. Serum specimens were pipetted into screw-capped plastic vials and frozen at -20°C. Frozen serum specimens were sent from Cambodia to the Special Pathogens Branch, Division of Viral and Rickettsial Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia. On arrival, the serum specimens were tested for antibodies to Nipah virus by enzyme immunoassay (EIA).

Of 96 serum specimens from the fruit bat (Pt. lylei), 11 (11.5%) were positive (>1/10) for Nipah virus antibodies by EIA. All 11 were confirmed by serum neutralization test. Nine additional sera were found positive (low titers) only by neutralization assay. We also screened sera (when sufficient quantities were available) by neutralization test against HeV. In general, results were equivalent between the two tests. No sera were found positive for HeV and negative for Nipah virus. Our results suggest that the virus circulating in Cambodia is neither Nipah nor HeV, but another closely related virus.

Conclusions

Several species of the genus Pteropus show serologic evidence of Nipah or HeV infection. Attempts by several groups to recover virus from tissues of serologically positive bats have been unsuccessful, as have immunohistochemical tests to detect the infection in tissues (9). Several possible reasons may account for the inability to recover virus from serologically positive bats. Antibody-positive bats may represent the portion of those infected that survived and cleared the virus. Experimental inoculation of a small number of Australian Pteropus bats with a related paramyxovirus resulted in findings that the virus replicates, causes microscopic lesions, and is shed; the virus appears to clear as the antibody response appears (13,14). We did not attempt to isolate virus from blood, and our attempts to detect virus antigen in tissues by immunohistochemical tests in one bat were unsuccessful.

We observed no evidence that HeV (15) or Nipah viruses move directly from bats to humans. However, during the outbreak of Nipah virus encephalitis outbreak in Malaysia, several laboratory-confirmed Nipah cases that lacked exposure to infected pigs were identified (P. Kitsutani, pers. comm.). In Cambodia, the distribution of Pt. lylei is limited to sites where they are protected from hunting, including urban areas and temples, where the human-bat interaction may be increased. The fact that these large bats are caught and used for food further increases the risk for exposure and infection in humans.

Future studies should include an evaluation of the risk of Nipah virus infection among populations intensely exposed to bats, such as those who capture, transport, slaughter, and butcher bats, as well as bat rehabilitators, animal caretakers, and wildlife conservationists. We suggest that future studies also include a cross-sectional survey of swine in Cambodia. Unlike workers on the large, commercial swine production farms of Malaysia, typical swine farmers in Cambodia raise several swine for their own use and for the local market. The potential for amplification of the virus, unlike that observed in the large concentrated pig population in Malaysia, remains very limited. Finally, a systematic study of encephalitis causes may show whether Nipah virus causes disease in humans in Cambodia and elsewhere in the region.

Dr. Olson is laboratory manager/epidemiologist at the Naval Medical Research Unit Number 2 satellite laboratory located at the National Institute of Public Health, Phnom Penh, Cambodia. His interests include the epidemiology and diagnosis of viral and rickettsial diseases.

Top

Acknowledgment

We thank Deborah Cannon, Jennifer Jones, Leilani Alvarez Kostiuchenko, Emily Meseck, Marty Monroe, Benjamin Shapiro, and Thomas Stevens for their participation in collecting and processing specimens and performing laboratory procedures.

Top

References

  1. Chua  KB, Goh  KJ, Wong  KT, Kamarulzaman  A, Tan  PSK, Ksiazek  TG, Fatal encephalitis due to Nipah virus among pig-farmers in Malaysia. Lancet. 1999;354:12579. DOIPubMedGoogle Scholar
  2. Centers for Disease Control and Prevention. Update: outbreak of Hendra-like virus—Malaysia and Singapore, 1998–1999. MMWR Morb Mortal Wkly Rep. 1999;48:2659.PubMedGoogle Scholar
  3. Centers for Disease Control and Prevention. Update: outbreak of Nipah virus—Malaysia and Singapore, 1999. MMWR Morb Mortal Wkly Rep. 1999;48:3357.PubMedGoogle Scholar
  4. Paton  NI, Leo  YS, Zaki  SR, Auchus  AP, Lee  KE, Ling  AE, Outbreak of Nipah-virus infection among abattoir workers in Singapore. Lancet. 1999;354:12536. DOIPubMedGoogle Scholar
  5. Chua  KB, Bellini  WJ, Rota  PA, Harcourt  BH, Tamin  A, Lam  SK, Nipah virus: a recently emergent deadly paramyxovirus. Science. 2000;288:14325. DOIPubMedGoogle Scholar
  6. O'Sullivan  JD, Allworth  AM, Paterson  DL, Snow  TM, Boots  R, Gleeson  LJ, Fatal encephalitis due to novel paramyxovirus transmitted from horses. Lancet. 1997;349:935. DOIPubMedGoogle Scholar
  7. Daniels  P, Aziz  J, Ksiazek  T, Ong  BL, Bunning  M, Johara  B, Nipah virus –considerations for regional preparedness. In: Classical swine fever and emerging diseases in Southeast Asia. Canberra: Australian Centre for International Agricultural Research, 1999. p. 133–41.
  8. Nor  MNM. Nipah disease in Malaysia. In: Disease Information. Paris:Office International des Epizooties 1999;12:67–70.
  9. Yob  JM, Field  H, Rashdi  AM, Morrissy  C, van der Heide  B, Rota  P, Nipah virus infection in bats (order Chiroptera) in peninsular Malaysia. Emerg Infect Dis. 2001;7:43941.PubMedGoogle Scholar
  10. Chua  KB, Koh  CL, Hooi  PS, Wee  KF, Khong  JH, Chua  BH, Isolation of Nipah virus from Malaysian Island flying-foxes. Microbes Infect. 2002;4:14551. DOIPubMedGoogle Scholar
  11. Halpin  K, Young  PL, Field  H, Mackenzie  JS. Newly discovered viruses of flying foxes. Vet Microbiol. 1999;68:837. DOIPubMedGoogle Scholar
  12. Halpin  K, Young  PL, Field  H, Mackenzie  JS. Isolation of Hendra virus from Pteropid bats: a natural reservoir of Hendra virus. J Gen Virol. 2000;81:192732.PubMedGoogle Scholar
  13. Williamson  MM, Hooper  PT, Selleck  PW, Westbury  HA, Slocombe  RF. Experimental Hendra virus infection in pregnant guinea-pigs and fruit bats (Pteropus poliocephalus). J Comp Pathol. 2000;122:2017. DOIPubMedGoogle Scholar
  14. Williamson  MM, Hooper  PT, Selleck  PW, Gleeson  LJ, Daniels  PW, Westbury  HA, Transmission studies of Hendra virus (equine morbillivirus) in fruit bats, horses and cats. Aust Vet J. 1998;76:8138. DOIPubMedGoogle Scholar
  15. Selvey  L, Taylor  R, Arklay  A, Gerard  J. Screening of bat carers for antibodies to equine morbillivirus. Commun Dis Intell. 1996;20:4778.

Top

Cite This Article

DOI: 10.3201/eid0809.010515

Table of Contents – Volume 8, Number 9—September 2002

EID Search Options
presentation_01 Advanced Article Search – Search articles by author and/or keyword.
presentation_01 Articles by Country Search – Search articles by the topic country.
presentation_01 Article Type Search – Search articles by article type and issue.

Top

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

Thomas G. Ksiazek, Special Pathogens Branch, MS G14, Centers for Disease Control and Prevention, 1600 Clifton Rd., Atlanta, GA 30333, USA; fax: 404-639-1118;

Send To

10000 character(s) remaining.

Top

Page created: July 16, 2010
Page updated: July 16, 2010
Page reviewed: July 16, 2010
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external