Volume 15, Number 7—July 2009
Ranavirus Outbreak in North American Bullfrogs (Rana catesbeiana), Japan, 2008
To the Editor: Ranaviruses (family Iridoviridae) are emerging pathogens of farmed and wild amphibians and cause high mortality rates in these animals (1). These viruses are associated with massive population decreases of some species (2,3); outbreaks have been reported in the United States, Asia, Micronesia, and Europe. At the general meeting held by the International Epizootic Office in May 2008, iridoviruses of amphibians were added to the list of pathogens of wildlife that should be monitored (www.oie.int/aac/eng/Publicat/Cardsenglish/Ranavirus%20card_final.pdf, www.oie.int/eng/normes/fcode/en_chapitre_2.4.2.htm, and www.jcu.edu.au/school/phtm/PHTM/frogs/otherdiseases-viruses.htm). We report an outbreak of ranavirus disease in amphibians in Japan.
A mass die-off of wild North American bullfrog (Rana catesbeiana) larvae was discovered in a 1,000-m2 pond in western Japan. The die-off lasted from September 10 through October 20, 2008, with an epidemic peak on September 20, during which several thousand carcasses were collected daily. No dead adults of R. catesbeiana or other amphibian species were found. Fish (families Cyprinidae and Gobiidae) in the pond were unaffected.
Clinical signs in frogs were depression; lethargy; palpebral hyperemia; abdominal edema, petechiae, and erythema on the ventral surface; skin ulcers; limb and tail necrosis; and emaciation. Pathologic changes were similar in all larvae. At necropsy, subcutaneous edema, body cavity effusions, and swollen and friable livers were observed. Histologic examination showed extensive glomerular necrosis with renal tubular hyaline droplet degeneration (Appendix Figure) and various degrees of hepatic cell degeneration and necrosis. Myxosporidia were not observed within any renal tubules. Electron microscopy showed cytoplasmic ranavirus-like particles within glomerular endothelial cells. These particles were icosahedral with a diameter of ≈120 nm. Bacterial colonies were observed on the skin and within multiple organs in some larvae examined. These colonies were interpreted to be opportunistic organisms and microbial cultures were not performed.
PCR with primers M153 and M154 (4) amplified a ranavirus-specific gene encoding major capsid protein (MCP) from 18 bullfrog specimens. DNA sequences (584 nt, which did not include primer-annealing regions) obtained from 5 PCR products randomly selected by direct-sequencing were identical. These sequences showed highest similarities with those of R. catesbeiana virus TW07–440 (GenBank accession no. FJ207464); only 1 nt difference was observed and this difference resulted in an amino acid substitution. Amplifications with several sets of primers (M68/M69, M70/M71, M72/M73, M84/M85, and M151/M152) (4) and sequencing were conducted.
We determined MCP DNA sequences of 1,472 nt that included the complete coding region (nt positions 17–1408, 1,392 nt) and proximal flanking regions. Sequences were deposited in the DNA Data Bank of Japan/GenBank/European Molecular Biology Laboratory DNA databases under the accession no. AB474588. Phylogenetic analysis showed that virus detected in this study, designated RCV-JP, showed greater similarity to TW07–440 virus than to other ranaviruses, including tadpole edema virus (5), frog virus 3 (6), and R. catesbeiana virus Z (7). Liver tissues of fish (Gnathopogon spp.) that cohabitated the pond, but showed no external signs of disease, were positive for ranavirus by PCR using primers M153 and M154. Further sequence analyses are ongoing, and additional investigations of other amphibians and fishes are needed.
Live freshwater fish from several countries have been imported into Japan. However, large amounts (<1,300 tons in 2007) of live aquaculture products, including eels and other fishes, have been imported from Taiwan into Japan (www.customs.go.jp/tariff/2007_4/data/03.htm). Given that viruses that originate in Japan and Taiwan are similar, the ranavirus we detected was likely imported into Japan in an infected aquatic organism. However, an epidemiologic survey will be necessary to determine the source of the ranavirus in the pond studied. Likewise, this virus may be endemic to Japan, and a survey of native and foreign free-ranging amphibians should be conducted. Molecular analysis of ranaviruses detected in these surveys will be necessary to differentiate endemic viruses from introduced viruses.
Japan is located at middle latitudes and has a temperate climate. This country has long been geologically isolated from Asia. This isolation has resulted in the development of many diverse species of amphibians in Japan; 23 species of the order Caudata and 35 species of the order Anura. Of these species, 49 (84%) are native and 36 (62%) are listed by the Ministry of the Environment as threatened species (8). R. catesbeiana frogs were introduced into Japan in 1918 as a food animal, and raising them by aquaculture was widely attempted. Although they are no longer cultured, feral populations have become established throughout Japan (9). Ranavirus in R. catesbeiana frogs represents a serious threat to amphibians throughout Japan.
This study was supported by the Global Environment Research Fund (F-3 and F-081) of the Ministry of the Environment, Japan, 2008, and The Promotion and Mutual Aid Corporation for Private Schools of Japan, Grant in Aid for Matching Fund Subsidy for Private Universities.
- Daszak P, Berger L, Cunningham AA, Hyatt AD, Green DE, Speare R. Emerging infectious diseases and amphibian population declines. Emerg Infect Dis. 1999;5:735–48.
- Cunningham AA, Hyatt AD, Russell P, Bennett PM. Emerging epidemic diseases of frogs in Britain are dependent on the source of ranavirus agent and the route of exposure. Epidemiol Infect. 2007;135:1200–12.
- Docherty DE, Meteyer CU, Wang J, Mao J, Case ST, Chinchar VG. Diagnostic and molecular evaluation of three iridovirus-associated salamander mortality events. J Wildl Dis. 2003;39:556–66.
- Marsh IB, Whittington RJ, O’Rourke B, Hyatt AD, Chisholm O. Rapid differentiation of Australian, European and American ranavirus based on variation in major capsid protein gene sequence. Mol Cell Probes. 2002;16:137–51.
- Wolf K, Bullock GL, Dunbar CE, Quimby MC. Tadpole edema virus: a viscerotropic pathogen for anuran amphibians. J Infect Dis. 1968;118:253–62.
- Miller DL, Rajeev S, Gray MJ, Baldwin CA. Frog virus 3 infection, cultured American bullfrogs. Emerg Infect Dis. 2007;13:342–3.
- Majji S, LaPatra S, Long SM, Sample R, Bryan L, Sinning A, Rana catesbeiana virus Z (RCV-Z): a novel pathogenic ranavirus. Dis Aquat Organ. 2006;73:1–11.
- Ota H. Current status of the threatened amphibians and reptiles of Japan. Popul Ecol. 2000;42:5–9.
- Maeda N, Matsui M. Frogs and toads of Japan. Tokyo: Bun-Ichi Sogo Shuppan Publishers; 1989. p. 100–7.
Suggested citation for this article: Une Y, Sakuma A, Matsueda H, Nakai K, Murakami M. Ranavirus outbreak in North American bullfrogs (Rana catesbeiana), Japan, 2008 [letter]. Emerg Infect Dis [serial on the Internet]. 2009 Jul [date cited]. Available from http://wwwnc.cdc.gov/eid/article/15/7/08-1636
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