Detection of Infectious Fungal Diseases of Frogs Inhabiting in Korea

Abstract

In recent years, there has been a rapid decrease in amphibian populations worldwide, and infectious diseases have been associated with this decline. Diseased frogs inhabiting Korea were collected from fields, and the diseases were identified by morphological and molecular analyses. Two fungal diseases-saprolegniasis and chromomycosis-were detected in the frogs. Saprolegniasis caused by Saprolegnia spp. was found in Rana plancyi chosenica from Gangwon-do and Rana huanrenensis from Chungbuk. Chromomycosis, which is caused by infection with Cladosporium cladosporioides, was detected in Rana catesbeiana from Busan.

Many factors are known to be related with the worldwide decline in amphibian populations (Alford and Richards, 1999; Beebee and Griffiths, 2005). Although the precise causes for the declines remain to be determined yet, modifications in the physical habitat, infectious diseases, predation by exotics, and changes in environmental conditions such as increased exposure to ultraviolet radiation and acid precipitation are known to be closely associated with the decline in the amphibian populations (Gardner, 2001). Blaustein and Kiesecker (2002) suggested that the declines were the result of complex interactions among multiple factors and that the causative factors differed among regions.

Recently, there are increasing reports of infectious diseases as the cause of the global decline in amphibian populations (Daszak et al., 1999; Longcore et al., 1999). A variety of diseases, including chytridiomycosis, ranavirus disease, and saprolegniasis, have been generally accepted to play a major role in the high mortality in amphibian populations worldwide (Berger and Speare, 1998; Daszak et al., 1999; Pessier et al., 1999). Infectious fungal diseases affecting frogs include chytridiomycosis, chromomycosis, mucormycosis, and saprolegniasis. In particular, chytridiomycosis that is caused by Batrachochytrium dendrobatidis has received recent attention with high mortality of amphibian populations around the world. The other fungal disease saprolegniasis that is caused by pathogenic oomycetes, namely, Saprolegnia spp., has also been considered responsible for the high mortality in amphibians. Infection is due to the complex interactions of pathogens with environmental factors (Kiesecker and Blaustein, 1995; Kiesecker et al., 2001).

Studies have suggested that disease outbreaks are often the result of complex interactions among many biotic and abiotic factors and are responsible for the decline in the amphibian populations (Blaustein and Kiesecker, 2002). Therefore, along with the increasing efforts that are recently being adopted to control environmental factors, disease control should also be implemented in conservation and reintroduction of amphibians. However, despite the significance of infectious fungal diseases among amphibian diseases, there has been no systematic study regarding them in Korea. In this study, diseased frogs from Korea were collected from field sites and a frog farm, and their diseases were identified using morphological and molecular analyses.

Materials and Methods

Diseased frogs were collected between 2006 and 2007 from various regions, including farms. Three diseased species of frogs were found from fields and a frog farm in Korea: Gold-spotted frog (Rana plancyi chosenica) tadpoles from a farm in Chuncheon, Gangwon-do; American Bullfrog (Rana catesbeiana) specimens from a reservoir in Gijang-gun, Busan; and adult Korean Stream Brown frogs (Rana huanrenensis) from a ditch in Chun Taesan, Yeongdong-gun, Chungbuk. A landing net was used to catch the frogs. The dead frogs were put into a bag containing pieces of ice, transported to the laboratory, and stored in a freezer until use.

The diseased fogs were observed, and their characteristics were recorded using light microscopes. Diseases were identified based on morphological characteristics. For molecular identification of the pathogens, skin tissue or infected intestinal parts were removed, and DNA was extracted following the protocol of the DNeasy Plant Mini Kit (Qiagen Science, USA). The DNA was amplified using Prime Taq Premix (G-2000) obtained from GENET (mixing solution [pH 9.0] with a 1 ml microtube, 1 units/10 µl Prime Taq DNA polymerase, 2× reaction buffer, 4 mM MgCl₂, enzyme stabilizer, loading dye, and 2 mM dNTPs). Using the universal fungal primer pairs ITS1 (5'-TCCGCAGGTTCACCTACGGA-3') and ITS4 (5'-TCCTCCGCTTATTGATATGC-3'), the internal transcribed spacer1 (ITS1) and internal transcribed spacer4 (ITS4) regions were amplified (Bruns and Gardes, 1993). After adjusting the total volume to 20 µl with 10 pM of ITS1 of Prime Taq Premix and 2 µl ITS4 primer, 2 µl template DNA (20 ng), and 4 µl pure water, PCR was performed using a thermal cycler (Applied Biosystems). The PCR protocol was as follows: 1 cycle at 94℃ for 4 min; followed by 35 cycles at 94℃ for 1 min, 54℃ for 1 min, and 72℃ for 1 min; and 1 cycle at 72℃ for 4 min. The PCR products were sequenced using the AMI PRISM 377 automated sequencer (Perkin-Elmer, USA). A sequence similarity search of the National Center for Biotechnology Information (NCBI) database was conducted using the Basic Local Alignment Search Tool (BLAST) algorithm.

Results and Discussion

Symptoms of two infectious diseases, namely, saprolegniasis and chromomycosis, were observed in the three species of frogs. Diseased Korean Golden frog (R. plancyi choseni) tadpoles were found in a frog farm in 2006. A fuss-like mold was observed on most parts of the tadpole tail or head (Fig. 1A). The PCR products that were amplified from the diseased tissue were 750 bp and nucleotide sequence analysis showed that the sequence had the closest similarity with Saprolegnia australis (Genebank accession no. AM228837.1, Table 1). It is highly possible that the disease affecting the R. plancyi choseni individuals in this study was saprolegniasis. Saprolegniasis was also detected in wild frogs and Korean Stream Brown frogs (R. huanrenensis). The diseased frogs presented with an eye infected by the pathogen (Fig. 1B). One eye of the diseased frogs was covered with white mold, and their legs were swollen. The frogs moved slowly and died after being transported to the lab. It has been reported that the skin of frogs with saprolegniasis is covered with a characteristic matted white cotton-like material (Pessier, 2002). The R. plancyi choseni and R. huanrenensis specimens that we studied presented with the same symptoms. The PCR product from the infected tissue was 700 bp, and the sequence was closest to Saprolegnia diclina (Table 1). Saprolegniasis is caused by infectious oomycetous water molds such as Saprolegnia, Aphanomyces, and Achlya. It is known as a common disease affecting frog eggs and tadpoles in frog farms (Anver and Pond, 1984).

Fig. 1.

Morphological feature showing symptoms of diseased frogs found in Korea. A. a tadpole of Gold-spotted pond frog (Rana plancyi chosenica) infected by Saprolegnia australis. Mold like fuss was observed in in the head. B. Korean stream brown frog (Rana huanrenensis) infected by Saprolegnia diclina. The symptom was observed in one eye. C. American Bullfrog (Rana catesbeiana) infected by Cladosporium cladosporioides. Red spots in the thigh and abdomen, gray-black pigmentation in the side were observed.

Table 1.

Diseases of frogs identified by sequence analysis

Diseased American Bullfrogs (R. catesbeiana) were found around a reservoir in Busan. Black molds and red spots on the flesh on the inside of the thigh and the flank were observed in these frogs (Fig. 1C). The other seven frogs found at the site showed the same symptoms. The morphological characteristics of this disease were identical to those described by Gonzalez-Mendoza (1988). The PCR product that was amplified from the DNA extracted tissue of the diseased frog was 600 bp, and its nucleotide sequence was closest to Cladosporium cladosporioides (Table 1). C. cladosporioides has been known to be the representative pathogen causing chromomycosis in amphibians (Roberts, 1986). Molecular analysis showed that the disease infecting R. catesbeiana in this study was likely to be chromomycosis. In this study, two infectious diseases were found to affect frogs collected from a frog farm and field sites in Korea. Our result can be used as the framework for studying infectious amphibian diseases in Korea. Further research will help in protecting against the extinction of amphibian species due to infectious diseases in Korea.