Serotyping and antimicrobial resistance profile of Salmonella spp. isolated from crocodilians in captivity
Serotipificación y perfil de resistencia antimicrobiana de Salmonella spp. aislados de crocodilios en cautiverio
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Objective. Determine the presence of Salmonella spp and the AMR in isolates of cloacal and muscle swabs in specimens of Caiman crocodilus fuscus and Crocodylus acutus in captivity, in Colombia. Materials and methods. A cross-sectional and descriptive sampling was carried out with a non-probabilistic design for convenience, once, during the month of February 2021. 150 Caiman crocodilus fuscus and Crocodylus acutus animals were included, with a 50/50 distribution. Cloacal and muscle samples were taken with sterile swabs. These were planted on MacConkey agar, then on SS agar. These positive samples were then reconfirmed on TSI agar. Serotyping was performed with specific monovalent and polyvalent antisera. The diffusion test was performed on Mueller-Hinton agar. Results. There was no growth of colonies in any muscle sample. The presence of the bacteria in cloacal samples of Caiman crocodilus fuscus was 36% and for Crocodylus acutus 50.6%. The serotypes with the highest detection percentage in both groups were serogroup C1 and polyvalent serogroup B. Some colonies were resistant to tetracycline, while other colonies had intermediate resistance to ampicillin, cefoxitin, sulfa trimethoprim, and tetracycline. Conclusions. This is the first report related to the detection of Salmonella spp. in alligator carcasses in the country, without finding the presence of the agent in any sample evaluated, however, the importance of continuing its monitoring is emphasized to guarantee innocuous products
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- Boede E, Sogbe E. Enfermedades en caimanes del orinoco (Crocodylus intermedius) y caimanes de la costa (Crocodylus acutus) mantenidos en zoocriaderos venezolanos. Rev Cient FCV-LUZ. 2000; 1(4):328-338. https://produccioncientificaluz.org/index.php/cientifica/article/view/14718
- Uhart M, Ferreyra H, Mattiello R, Caffés M, Terragno R, Schettino A, Prado W. Isolation of Salmonella spp. from yacare caiman (Caiman yacare) and broad-snouted caiman (Caiman latirostris) from the argentine chaco. J Wildlife Dis. 2011; 47(2):271-277. http://dx.doi.org/10.7589/0090-3558-47.2.271.
- Targino T, Quadros P, Cardoso Y, Saraiva J, Neris D, Curbani F, et al. Predominant bacterial microbiota of the mouth and cloaca from captive Caiman latirostris (Daudin, 1802). Herpetol Notes. 2020; 13:451-455. https://www.biotaxa.org/hn/article/view/58133/61421
- Grijalba J, Forero E, Contreras A, Vargas J, Andrade R. Determination of hematological values of common crocodile (Caiman crocodilus fuscus) in captivity in the Magdalena medio of Colombia. Acta biol Colomb. 2019; 25(1):75-81. http://dx.doi.org/10.15446/abc.v25n1.76045
- Canto A, Costa-Lima B, Suman P, Monteiro M, Marsico T, Conte-Junior C, et al. Fatty acid profile and bacteriological quality of caiman meat subjected to high hydrostatic pressure. J Food Sci Technol. 2015; 63:872–877. https://doi.org/10.1016/j.lwt.2015.05.003
- Hoffman L, Cawthorn D. What is the role and contribution of meat from wildlife in providing high-quality protein for consumption? Anim Front. 2012; 2:40–53. https://doi.org/10.2527/af.2012-0061
- Hoffman L, Cawthorn D. Exotic protein sources to meet all needs. Meat Sci. 2013; 95:764–771. https://doi.org/10.1016/j.meatsci.2013.04.027
- Vilhena A, Guerra M, Carneiro B, Aquiles C, Teixeira E, Pimentel T, et al. 2018. Effect of UV-C radiation on Salmonella spp. reduction and oxidative stability of caiman (Caiman crocodilus yacare) meat. J Food Saf. 2018; e12604. https://doi.org/10.1111/jfs.12604
- Yang S, Sadekuzzaman M, Ha S. Treatment with lauric arginate ethyl ester and commercial bacteriophage, alone or in combination, inhibits Listeria monocytogenes in chicken breast tissue. Food Control. 2017; 78:57–63. https://doi.org/10.1016/j.foodcont.2017.02.021
- Pachón D, Pulido A, Moreno C. Aislamiento y serotipificación de Salmonella sp. en estanques con Crocodylus intermedius y testudines cautivos en Villavicencio – Colombia. Rev MVZ Córdoba. 2011; 16(2):2564-2575. https://revistamvz.unicordoba.edu.co/article/view/1021
- Monteiro M, Mársico E, Mano B, Alvares S, Rosenthal A, Lemos M, et al. Combined effect of high hydrostatic pressure and ultraviolet radiation on quality parameters of refrigerated vacuum-packed tilapia (Oreochromis niloticus) fillets. Sci Rep. 2018; 8:9524. https://doi.org/10.1038/s41598-018-27861-9
- Rodrigues B, Alvares T, Sampaio G, Cabral C, Araujo J, Franco R, et al. Influence of vacuum and modified atmosphere packaging in combination with UV-C radiation on the shelf life of rainbow trout (Oncorhynchus mykiss) fillets. Food Control. 2016; 60:596–605. https://doi.org/10.1016/j.foodcont.2015.09.004
- Santos J, Mársico E, Lemos M, Cinquini M, Silva F, Dutra Y, et al. 2018. Effect of the UV-C radiation on shelf life of vacuum-packed refrigerated pirarucu (Arapaima gigas) fillets. J Aqua Food Prod Tech 27:48–60. https://doi.org/10.1080/10498850.2017.1402840
- Grimont P, Weill F. Antigenic Formulas of the Salmonella Serovars. 9a ed. World Health Organization- Institut Pasteur. París, Francia; 2007. https://www.pasteur.fr/sites/default/files/veng_0.pdf
- Gay N, Le Hello S, Weill F, Thoysi B, Berger F. Salmonella serotypes in reptiles and humans, French Guiana. Vet Microbiol. 2014; 170(1-2):167-171 https://doi.org/10.1016/j.vetmic.2014.01.024
- Merkeviciene L, Butrimaite-Ambrozeviciene C, Paškevicius G, Pikuniene A, Virgailis M, Dailidaviciene J, et al. Serological variety and antimicrobial resistance in salmonella isolated from reptiles. Biology. 2022; 11(6):836. https://doi.org/10.3390/biology11060836
- Bauwens L, Vercammen F, Bertrand S, Collard J, De Ceuster S. Isolation of Salmonella from environmental samples collected in the reptile department of Antwerp Zoo using different selective methods. J Appl Microbiol. 2006; 101(2):284-289. https://dx.doi.org/10.1111/j.1365-2672.2006.02977.x
- Maluta A, Zajac M, Krajewska-Wedzina M, Wasyl D, Heckers K, Didkowska A, et al. Mixed Infection of Mycobacterium szulgai, M. lentiflavum, and Gram-Negative Bacteria as a Cause of Death in a Brown Caiman Caiman crocodylus: A Case Report. J Vet Sci. 2022; 9:133. https://doi.org/10.3390/vetsci9030133
- Silva J, Mota R, Pinheiro J, Almeida M, Ferreira D, Azevedo J. Aerobic bacterial microflora of Broad-snouted caiman (Caiman latirostris) oral cavity and cloaca, originating from parque Zoológico Arruda Câmara, Paraíba, Brazil. Braz J Microbiol. 2009; 40(1):194-198. https://dx.doi.org/10.1590/S1517-838220090001000034.
- Carvalho G, Bérgamo A, Aleixo V, Veiga A, Moreira L, Knöbl T, et al. Hematological parameters and frequency of Salmonella spp. in swabs of caiman yacare after of probiotics. RICA. 2018; 9(5):51-63. http://doi.org/10.6008/CBPC2179-6858.2018.005.0006
- Ríos R, Flores B, Mora-Sánchez B, Torres D, Sheleby-Elías J, Jirón W, et al. Isolation of Salmonella spp. from black spiny-tailed iguana (Ctenosaura similis) meat commercialized in markets of León city, Nicaragua. Vet Med Sci. 2022; 8:695–699. https://doi.org/10.1002/vms3.654
- Morrison BJ, Rubin J. Detection of multidrug-resistant Gram-negative bacteria from imported reptile and amphibian meats. J Appl Micriobiol. 2020; 129(4):1053–1061. https://doi.org/10.1111/jam.14658
- O’Neal L, Alvarez D, Mendizábal-Cabrera R, Ramay BM, Graham J. Community-Acquired Antimicrobial Resistant Enterobacteriaceae in Central America: A One Health Systematic Review. Int J Environ Res Public Health. 2020; 17(20):7622. https://doi.org/10.3390/ijerph17207622