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Volume 21, Number 12—December 2015
Letter

Surveillance for Ebola Virus in Wildlife, Thailand

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To the Editor: Active surveillance for zoonotic pathogens in wildlife is particularly critical when the pathogen has the potential to cause a large-scale outbreak. The recent outbreak of Ebola virus (EBOV) disease in West Africa in 2014 was initiated by a single spillover event, followed by human-to-human transmission (1). Projection of filovirus ecologic niches suggests possible areas of distribution in Southeast Asia (2). Reston virus was discovered in macaques exported from the Philippines to the United States in 1989 and in sick domestic pigs in the Philippines in 2008 (with asymptomatic infection in humans) (3). Dead insectivorous bats in Europe were found to be infected by a filovirus, similar to other members of the genus Ebolavirus (4).

Although EBOV has historically been viewed as a virus from Africa, recent studies found that bat populations in Bangladesh and China contain antibodies against EBOV and Reston virus recombinant proteins, which suggests that EBOVs are widely distributed throughout Asia (5,6). Thus, an outbreak in Asian countries free of EBOV diseases may not only be caused by importation of infected humans and/or wildlife from Africa but may arise from in-country filovirus–infected wildlife. Serologic and molecular evidence for filoviruses suggests that members of the order Chiroptera (bats) may be their natural reservoir (7).

As part of a proactive biosurveillance program, we conducted a cross-sectional study for EBOV infection in bats and macaques in Thailand. We screened 500 Pteropus lylei bats collected from 10 roosting sites during March–June 2014 (Technical Appendix Figure) for antibodies against EBOV antigen by using an ELISA validated by the Centers for Disease Control and Prevention (Atlanta, GA, USA) (8).

Bats and macaques were captured with permission from the Department of National Parks, Wildlife and Plant Conservation. The Institutional Animal Care and Use Committee at the University of California, Davis (protocol #16048) approved the capture and sample collection protocols.

To further screen a wide range of wildlife species in Thailand for active EBOV infection, we sampled and tested 699 healthy bats, representing 26 species, and 50 long-tailed macaques (Macaca fascicularis). Additional bat species were randomly captured (≥50/site) in 6 provinces in Thailand during 2011–2013 and identified by morphologic traits. Macaques were captured and sampled in March 2013 from 1 site at Khao Chakan, Srakaeo Province, and released at the same site. Blood, saliva, urine, and feces were collected from anesthetized macaques or nonanesthetized bats. All animals were released after sample collection. Details on species screened, sample sizes, and trapping localities are provided in the Table.

All nonblood specimens were collected in nucleic acid extraction buffer (lysis buffer) and transported on ice to the World Health Organization Collaborating Centre for Research and Training on Viral Zoonoses laboratory (Bangkok, Thailand) for storage and testing. Three types of specimen (saliva, urine, and serum) were collected from individual animals and pooled.

Nucleic acid was then extracted with NucliSENS easyMAG (bioMérieux, Boxtel, the Netherlands) and analyzed by reverse transcription PCR (RT-PCR). A consensus RT-PCR was used to screen for all known species of Ebola virus and Marburg virus, including EBOV (9). In total, 5 RT-PCRs were performed on each specimen, a regimen that included 4 sets of primers specific to known filoviruses and 1 degenerate primer set to detect novel viruses in this family. The sensitivity of RT-PCR on synthetic standard was 50–500 copies/reaction (9). We ran 3,745 PCRs, covering a range of assays, to increase detection sensitivity. All specimens examined were negative for filoviruses by EBOV ELISA and PCR (Table). For P. lylei ELISA screening, optical density values for all 500 bats ranged from 0.000 to 0.095, well below the potential positive cutoff value of 0.2.

Assuming a population size of ≈5,000 bats/roost and a sample size of 50 bats/site, we have 95% confidence that if >6% of the population had antibodies against EBOV antigen, we would have detected it. If we assume that all 500 animals are part of 1 large panmictic population, and we have 95% confidence that if EBOV were circulating in >0.5% of the population, we would have detected it. Therefore, although we cannot rule out infection of this species with 100% confidence, P. lylei bats, the most abundant species of large pteropid bats in Thailand, are highly unlikely to be reservoirs for EBOV.

Our sample sizes for PCR screening of other bat species in this study were much smaller, and we had no supported serologic data, but these negative results could add to the knowledge of filovirus infection in nontissue specimens from healthy bats. Previous studies have detected Ebola virus–like filovirus RNA in lung tissue of healthy Rousettus leschenaultia bats in China (10) and from organs and throat and rectal swab specimens from a die-off of Miniopterus schreibersii bats in Spain (4). In our study, which included 22 M. schreibersii and 132 M. magnate bats, none of the bats tested positive for filoviruses.One limitation of the cross-sectional sampling strategy used here, however, is that PCR-negative findings do not necessarily mean that the bats were not infected in the past. Although we found no evidence of filovirus infection in wildlife species tested in Thailand, we believe that continuing targeted surveillance in wildlife should enable early detection and preparedness to preempt emerging zoonoses.

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Acknowledgment

This study was supported by a research grant from Department of National Parks, Wildlife and Plant Conservation, the Thailand Research Fund (RDG5420089), the Ratchadaphiseksomphot Endowment Fund of Chulalongkorn University (RES560530148-HR), Health and Biomedical Science Research Program by National Research Council of Thailand and Health System Research Institute, the Research Chair Grant, the National Science and Technology Development Agency, Thailand, and the Naval Health Research Center (BAA-10-93) under the Cooperative Agreement no. W911NF-11-2-0041, and the United States Agency for International Development Emerging Pandemic Threats PREDICT project.

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Supaporn WacharapluesadeeComments to Author , Kevin J. Olival, Budsabong Kanchanasaka, Prateep Duengkae, Supakarn Kaewchot, Phimchanok Srongmongkol, Gittiyaporn Ieamsaard, Patarapol Maneeorn, Nuntaporn Sittidetboripat, Thongchai Kaewpom, Sininat Petcharat, Sangchai Yingsakmongkon, Pierre E. Rollin, Jonathan S. Towner, and Thiravat Hemachudha
Author affiliations: King Chulalongkorn Memorial Hospital and Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand (S. Wacharaplluesadee, N. Sittidetboripa, T. Kaewpom, S. Petcharat, S. Yingsakmongkon, T. Hemachudha); EcoHealth Alliance, New York, New York, USA (K.J. Olival); Department of National Parks, Bangkok (B. Kanchanasaka, S. Kaewchot, P. Srongmongkol, G. Ieamsaard, P. Maneeorn); Kasetsart University, Bangkok (P. Duengkae); Centers for Disease Control and Prevention, Atlanta, Georgia, USA (P.E. Rollin, J.S. Towner)

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References

  1. Gire  SK, Goba  A, Andersen  KG, Sealfon  RSG, Park  DJ, Kanneh  L, Genomic surveillance elucidates Ebola virus origin and transmission during the 2014 outbreak. Science. 2014;345:136972. DOIPubMedGoogle Scholar
  2. Peterson  AT, Bauer  JT, Mills  JN. Ecologic and geographic distribution of filovirus disease. Emerg Infect Dis. 2004;10:407. DOIPubMedGoogle Scholar
  3. Miranda  MEG, Miranda  NLJ. Reston ebolavirus in humans and animals in the Philippines: a review. J Infect Dis. 2011;204(Suppl 3):S75760. DOIPubMedGoogle Scholar
  4. Negredo  A, Palacios  G, Vázquez-Morón  S, González  F, Dopazo  H, Molero  F, Discovery of an ebolavirus-like filovirus in Europe. PLoS Pathog. 2011;7:e1002304. DOIPubMedGoogle Scholar
  5. Olival  KJ, Islam  A, Yu  M, Anthony  SJ, Epstein  JH, Khan  SA, Ebola virus antibodies in fruit bats, Bangladesh. Emerg Infect Dis. 2013;19:2703. DOIPubMedGoogle Scholar
  6. Yuan  JF, Zhang  YJ, Li  JL, Zhang  YZ, Wang  LF, Shi  ZL. Serological evidence of ebolavirus infection in bats, China. Virol J. 2012;9:236. DOIPubMedGoogle Scholar
  7. Olival  KJ, Hayman  DTS. Filoviruses in bats: current knowledge and future directions. Viruses. 2014;6:175988. DOIPubMedGoogle Scholar
  8. Rollin  P, Nichol  S, Zaki  S, Ksiazek  T. Arenaviruses and filoviruses. In: Versalovic J, Carroll K, Funke G, Jorgensen J, Landry M, Warnock D, editors. Manual of clinical microbiology. Washington (DC): ASM Press; 2011. p. 1514–29.
  9. Zhai  J, Palacios  G, Towner  JS, Jabado  O, Kapoor  V, Venter  M, Rapid molecular strategy for filovirus detection and characterization. J Clin Microbiol. 2007;45:2246. DOIPubMedGoogle Scholar
  10. He  B, Feng  Y, Zhang  H. Xu Lin, Yang W, Zhang Y, et al. Filovirus RNA in fruit bats, China [letter]. Emerg Infect Dis. 2015; 21:1675–77.

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Cite This Article

DOI: 10.3201/eid2112.150860

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Table of Contents – Volume 21, Number 12—December 2015

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Supaporn Wacharapluesadee, World Health Organization Collaborating Centre for Research and Training on Viral Zoonoses, King Chulalongkorn Memorial Hospital, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand

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Page created: November 10, 2015
Page updated: November 10, 2015
Page reviewed: November 10, 2015
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.
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