- Case Report
- Open Access
Tuberculosis caused by Mycobacterium bovis infection in a captive-bred American bullfrog (Lithobates catesbeiana)
© The Author(s). 2018
- Received: 4 June 2018
- Accepted: 16 September 2018
- Published: 21 September 2018
Tuberculosis is widely known as a progressive disease that affects endothermic animals, leading to death and/or economical losses, while mycobacterial infections in amphibians are commonly due to nontuberculous mycobacteria. To the authors’ knowledge, this report describes the first case of bovine tuberculosis in a poikilothermic animal.
An adult female captive American bullfrog (Lithobates catesbeianus Shaw, 1802) died in a Brazilian aquarium. Multiple granulomas with acid-fast bacilli were observed in several organs. Identification of Mycobacterium bovis was accomplished by culture and PCR methods. The other animals from the same enclosure were euthanized, but no evidence of mycobacterial infection was observed.
The American bullfrog was introduced in several countries around the world as an alternative husbandry, and its production is purposed for zoological and aquarium collections, biomedical research, education, human consumption and pet market. The present report warns about an episode of bovine tuberculosis in an amphibian, therefore further studies are necessary to define this frog species’ role in the epidemiology of M. bovis.
- Bovine tuberculosis
- Mycobacterium bovis
The genus Mycobacterium comprises several species, such as members of the Mycobacterium tuberculosis complex (MTBC) and other species known as nontuberculous mycobacteria (NTM) . Mycobacterium bovis belongs to the MTBC, and it is well-known for causing bovine tuberculosis and for its wide host range, including humans [1, 2]. There are reports of M. bovis infection in many species of mammals , while they are rare in birds .
In amphibians, mycobacterial infections are commonly caused by NTM, such as M. marinum, M. chelonae, M. fortuitum and M. ulcerans ecovar Liflandii, and are a common source of morbidity and mortality in captive animals . Natural transmission is still poorly understood, but most NTM infections in amphibians are thought to be opportunistic and acquired from environmental sources, such as soil, water and biofilms [5, 6].
International amphibians trade of captive-bred and wild-caught individuals has connected continents, as they are intended for zoological and aquarium collections, biomedical research, education [7, 8], human consumption [8, 9] and pet market [5, 7]. An example of a heavily traded amphibian is the American bullfrog (Lithobates catesbeianus Shaw, 1802). This species has been introduced in Central and South America, the Caribbean islands and Northeast and South-eastern Asia from North America, and it has been farmed for food, pet and biomedical research in many regions around the world [10, 11].
This report describes a case of tuberculosis caused by Mycobacterium bovis in a specimen of Lithobates catesbeianus kept in an aquarium and the potential zoonotic risk to the animal handlers.
A female American bullfrog (Lithobates catesbeianus) was acquired from a frog farm in the state of Sao Paulo that provided animals for meat, research institutes and schools. The animal was transferred to a public aquarium in Brazil, where it was maintained in a closed aqua-terrarium provided with adequate humidity, temperature and water quality. In the same enclosure, exclusive for bullfrogs, there were other three specimens. All of them were previously kept in quarantine for 30 days.
After five years in captivity, with no previous health problems, the animal showed an episode of regurgitation of a bloody fluid. During physical examination, anorexia and pale mucous membranes were observed and the animal was in shock. Despite attempt of supportive treatment with dexamethasone (1 mg/kg), enrofloxacin (1.5 mg/kg), and mixed amino acids and B-vitamins (0.5 ml, Mercepton®) by intramuscular administration, the animal died after 2 h.
At necropsy, 5 ml of translucent viscous fluid was observed in the coelomic cavity, and on cytological evaluation it showed a large amount of proteinaceous material, small numbers of erythrocytes, rare macrophages, lymphocytes and plasma cells, cellular debris and squamous epithelial cells. Macroscopically, isolated or agglomerated, 1.0 to 3.0 mm diameter, firm white-yellow nodules with caseous content were observed in the heart, lungs, liver, spleen, stomach, intestine, gonadal fat bodies and kidneys. The nodules were most frequent in the liver and spleen, and the spleen was firm and 3 to 4 times normal size.
Tissues samples from all organs were placed in 10% buffered formalin, and five-micrometer sections were obtained and stained using hematoxylin-eosin and Ziehl-Neelsen techniques. Microscopically, the lungs, spleen, intestine, liver, pancreas and kidneys had multiple granulomas, and large numbers of acid-fast bacilli (AFB) within macrophages consistent with a mycobacterial infection. Diffuse congestion, multifocal hemorrhage, extensive necrotic areas were observed in all organs, and marked hyperplasia of melanomacrophage centers were noted in spleen and liver.
Swab samples from all affected organs and the regurgitated bloody fluid were treated with 0.75% 1-Hexadecylpyridinium chloride (HPC), cultured in Stonebrink and Löwenstein-Jensen media, and incubated at 25 °C and 37 °C for 90 days. After approximately 35 days, mycobacterial isolates were observed in Stonebrink medium at 37 °C from all samples, and identified as Mycobacterium sp., MTBC, and M. bovis through previously described PCR methods, based on 16S rRNA gene, MPB70 gene  and genomic regions of difference (RD) , respectively.
Direct Variable Repeat Spacer Oligonucleotide Typing (DVR-Spoligotyping)  and the 24-locus set of mycobacterial interspersed repetitive-unit-variable-number tandem-repeat (MIRU-VNTR)  techniques were performed for genotyping. The M. bovis isolates were discriminated as SB2444 by the Mycobacterium bovis Spoligotyping Database (https://www.mbovis.org) and presented the unique pattern 2 2 5 3 2 2 3 3 2 2 6 3 4 4 4 0 5 3 3 3 2 7 1 2 through the MIRU-VNTR plus database (https://www.miru-vntrplus.org/MIRU/index.faces).
Despite the lack of clinical signs, the other animals in the enclosure were euthanized. They were firstly anesthetized with ketamine hydrochloride (100 mg/kg) and xylazine (10 mg/kg) by intracelomic administration (IC), followed by a lethal dose of pentobarbital sodium (60 mg/kg), IC. Necropsy, histopathological and bacterial examinations were performed, but no evidence of mycobacterial infection was observed.
Aquaculture of American bullfrogs for the meat industry has expanded worldwide during the twentieth century . Taiwan, Brazil, Ecuador and China are known for their significant production , while the United States of America, France, Canada, Belgium, Italy and Spain are known as great consumers . Brazil is the second largest producer of American bullfrogs in the world at approximately 400 tons per year . The success of the industry is attributable to the advantageous Brazilian climate and improvement of production systems that were expanded in the 1970’s and improved with the assistance of research institutions and universities , to provide controlled conditions for better efficiency.
To the authors’ knowledge, the present study describes the first report of infection by a member of the MTBC in a poikilothermic animal. Given the optimal growing temperature of MTBC is 37 °C, it is odd that a frog was able to develop bovine tuberculosis. However, the Brazilian climate can reach over 30 °C during winter, and higher temperatures are kept through climatized production systems.
Moreover, this bullfrog could be immunocompromised, considering the other animals showed no signs of infection. Similar disseminated granulomatous lesions caused by M. marinum were observed in American bullfrogs  and Japanese forest green tree frogs (Rhacophorus arboreus) . The coelomic effusion seen in the latter  and in the specimen of this case resembles the ascitic fluid caused by M. tuberculosis and M. bovis in humans . Accordingly, it is not surprising the use of M. marinum infection in fish and frogs as model for human tuberculosis .
The source of the M. bovis infection in this bullfrog was not determined. The aquarium handlers were tested for tuberculosis and presented negative results. Transmission by visitors is unlikely, since there is a glass barrier avoiding any contact to them. Also, each enclosure is isolated from the other and from any external contact, thus the infection probably occurred in the frog farm. Unfortunately, the information regarding the farm was lost during the aquarium personnel change.
Despite improvement of raniculture production systems, not all farms have adopted best management practices and some of them may supply the animals with crude protein feed from different sources. Given L. catesbeianus becomes carnivore in its adult stage [9, 10], our specimen might have acquired the infection from contaminated cow meat fed to the frog while in the farm. Other transmission possibilities could be through contact with an infected animal, whether from wildlife or another domestic animal source. Finally, an environmental source of infection cannot be excluded because while M. bovis is an obligate pathogen , it can survive in the environment for weeks depending on temperature, sunlight exposure, soil moisture and the presence of organic matter .
Although the genotyping techniques for bovine tuberculosis are purposed to track the origin of the infection, the profile found has not been reported in any study. Yet, it resembles the three most common spoligotypes in Brazil, SB0295, SB0121 and SB0120 , displaying two, three and four different spacers, respectively.
Isolation of M. bovis in captive American bullfrogs, either in breeding or research facilities and zoo collections, raises concerns for a new potential source of this highly zoonotic disease to workers in direct contact with these animals and for international movement as the result of trade in frog meat. Furthermore, the American bullfrog is ranked as one of the world’s most invasive species by the International Union for Conservation of Nature (IUCN) Invasive Species Specialist Group (ISSG)  and escape or release of frogs has resulted in feral populations .
Nevertheless, this case reports one episode of bovine tuberculosis in an amphibian, and further studies with experimental data are necessary to define if this frog species represents a potential reservoir or acts as spillover host of M. bovis.
We thank Dr. Mara Cristina Scheffer for her assistance in the spoligotyping technique.
Availability of data and materials
All data are presented in the manuscript.
Clinical stage: LR, BS; necropsy: LR, FAS; histopathologic evaluation: LR, FAS, CDP, APP; mycobacterial isolation and identification: CYI; writing of the manuscript: CYI, LR, JSFN, JLCD. All the authors revised and approved the final version of the manuscript.
Ethics approval and consent to participate
All data originated from retrospective clinical and diagnostic routine, without any experimental data. Therefore, the author’s institution (Aquario de Sao Paulo ethics committee) ruled that no formal ethics approval was required.
Consent for publication
The authors declare no competing interests.
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- Lécu A, Ball R. Mycobacterial infections in zoo animals: relevance, diagnosis and management. Int Zoo Yearb. 2011;45:183–202.View ArticleGoogle Scholar
- Miller M, Olea-Polpeka F. One health in the shrinking world: experiences with tuberculosis at the human–livestock–wildlife interface. Comp Immunol Microbiol Infect Dis. 2013;36:263–8.View ArticleGoogle Scholar
- Maas M, Michel AL, Rutten VPMG. Facts and dilemmas in diagnosis of tuberculosis in wildlife. Comp Immunol Microbiol Infect Dis. 2013;36:269–85.View ArticleGoogle Scholar
- Kelly P, Jahns H, Power E, Bainbridge J, Kenny K, Corpa JM, et al. Mycobacteriosis in ostriches (Struthio camelus) due to infection with Mycobacterium bovis and Mycobacterium avium complex. Avian Dis. 2013;57:808–11.View ArticleGoogle Scholar
- Martinho F, Heatley JJ. Amphibian mycobacteriosis. Vet Clin North Am Exot Anim Pract. 2012;15:113–9.View ArticleGoogle Scholar
- September SM, Brözel VS, Venter SN. Diversity of nontuberculoid Mycobacterium species in biofilms of urban and semiurban drinking water distribution systems. Appl Environl Microbiol. 2004;70:7571–3.View ArticleGoogle Scholar
- Schlaepfer MA, Hoover C, Dodd CK. Challenges in evaluating the impact of the trade in amphibians and reptiles on wild populations. BioScience. 2005;55:256–64.View ArticleGoogle Scholar
- Schloegel LM, Picco AM, Kilpatrick AM, Davies AJ, Hyatt AD, Daszak P. Magnitude of the US trade in amphibians and presence of Batrachochytrium dendrobatidis and ranavirus infection in imported north American bullfrogs (Rana catesbeiana). Biol Conserv. 2009;142:1420–6.View ArticleGoogle Scholar
- Cribb AY, Afonso AM, Mostério CMF. Manual Técnico de Raniculura. Brasília: Embrapa; 2013.Google Scholar
- FAO. Cultured Aquatic Species Information Programme. Rana catesbeiana. In: Fisheries and aquaculture department, 2005. http://www.fao.org/fishery/culturedspecies/Rana_catesbeiana/en. Accessed 28 March 2018.
- Both C, Lingnau R, Santos-Jr A, Madalozzo B, Lima LP, Grant T. Widespread occurrence of the American bullfrog, Lithobates catesbeianus (Shaw, 1802) (Anura: Ranidae), in Brazil. South Am J Herpetol. 2011;6:127–34.View ArticleGoogle Scholar
- Wilton S, Cousins D. Detection and identification of multiple mycobacterial pathogens by DNA amplification in a single tube. PCR Methods Appl. 1992;1:269–73.View ArticleGoogle Scholar
- Warren RM, Gey Van Pittius NC, Barnard M, Hesseling A, Engelke E, De Kock M, et al. Differentiation of Mycobacterium tuberculosis complex by PCR amplification of genomic regions of difference. Int J Tuberc Lung Dis. 2006;10:818–22.PubMedGoogle Scholar
- Kamerbeek J, Schouls L, Kolk A, van Agterveld M, van Soolingen D, Kuijper S, et al. Simultaneous detection and strain differentiation of Mycobacterium tuberculosis for diagnosis and epidemiology. J Clin Microbiol. 1997;37:907–14.Google Scholar
- Supply P, Allix C, Lesjean S, Cardoso-Oelemann M, Rüsch-Gerdes S, Willery E, et al. Proposal for standardization of optimized mycobacterial interspersed repetitive unit–variable-number tandem repeat typing of Mycobacterium tuberculosis. J Clin Microbiol. 2006;44:4498–510.View ArticleGoogle Scholar
- Fontana I, Cunha EAP. Change of the Brazilian health status towards OIE for amphibian diseases. Biológico. 2017;79:Supplement:89.Google Scholar
- Ferreira R, Fonseca L de S, Afonso AM, da Silva MG, Saad MH, Lilenbaum W. A report of mycobacteriosis caused by Mycobacterium marinum in bullfrogs (Rana catesbeiana). Vet J. 2006;171:177–80.View ArticleGoogle Scholar
- Haridy M, Tachikawa Y, Yoshida S, Tsuyuguchi K, Tomita M, Maeda S, Wada T, Ibi K, Sakai H, Yanai T. Mycobacterium marinum infection in Japanese forest green tree frogs (Rhacophorus arboreus). J Comp Pathol. 2014;151:277–89.View ArticleGoogle Scholar
- Cavalli Z, Ader F, Valour F, Saison J, Boussel L, Dumitrescu O, et al. Clinical presentation, diagnosis, and bacterial epidemiology of peritoneal tuberculosis in two university hospitals in France. Infect Dis Ther. 2016;5:193–9.View ArticleGoogle Scholar
- Duffield BJ, Young DA. Survival of Mycobacterium bovis in defined environmental conditions. Vet Microbiol. 1985;10:193–7.View ArticleGoogle Scholar
- Ghavidel M, Manssury D, Nourian K, Ghazvini K. The most common spoligotype of Mycobacterium bovis isolated in the world and the recommended loci for VNTR typing; a systematic review. Microb Pathog. 2018;118:310–5.View ArticleGoogle Scholar
- Global Invasive Species Database. Species profile: Lithobates catesbeianus. In: Invasive species specialist group, 2018. http://www.iucngisd.org/gisd/species.php?sc=80. Accessed 15 March 2018.
- Barrasso DA, Cajade R, Nenda SJ, Baloriani G, Herrera R. Introduction of the American bullfrog Lithobates catesbeianus (Anura: Ranidae) in natural and modified environments: an increasing conservation problem in Argentina. South Am J Herpetol. 2009;4:69–75.View ArticleGoogle Scholar