Diversity of Aerobic Bacteria Isolated from Oral and Cloacal Cavities from Free-Living Snakes Species in Costa Rica Rainforest
Costa Rica has a significant number of snakebites per year and bacterial infections are often complications in these animal bites. Hereby, this study aims to identify, characterize, and report the diversity of the bacterial community in the oral and cloacal cavities of venomous and nonvenomous snakes found in wildlife in Costa Rica. The snakes where captured by casual encounter search between August and November of 2014 in the Quebrada González sector, in Braulio Carrillo National Park. A total of 120 swabs, oral and cloacal, were taken from 16 individuals of the Viperidae and Colubridae families. Samples were cultured on four different media at room temperature. Once isolated in pure culture, colonies were identified with the VITEK® 2C platform (bioMérieux). In order to test the identification provided on environmental isolates, molecular analyses were conducted on 27 isolates of different bacterial species. Specific 16S rDNA PCR-mediated amplification for bacterial taxonomy was performed, then sequenced, and compared with sequences of Ribosomal Database Project (RDP). From 90 bacterial isolates, 40 different bacterial species were identified from both oral and cloacal swabs. These results indicate the diversity of opportunistic pathogens present and their potential to generate infections and zoonosis in humans.
Costa Rica is one of the countries with the highest rates of biodiversity per km2. It includes 143 species of snakes described. Within them, some species are venomous and potentially life-threatening to animals and humans: five species of coral snakes (family Elapidae, subfamily Elapinae), sixteen of pit vipers, such as Bothrops asper and Bothriechis schlegelii (family Viperidae, subfamily Crotalinae), and a sea snake (family Elapidae, subfamily Hydrophiinae) .
In tropical regions, snakebites are important health problems . Only in Central America, approximately 4000 snakebites have been registered per year, being the agricultural workers and/or rural residents the most affected [5, 6]. In Costa Rica, the average of snakebites was 504 reports per year during 1990 to 2000 . The study of these animals has focused greatly on poisonous species for their medical interest, since they are responsible for a significant number of snakebite incidents in the country .
During the period 1990–2000, a total of 5550 snakebite accidents were reported in hospitals and other health centers in Costa Rica. High variation was observed in the number of cases per year, ranging from 423 (1999) to 590 (1992). No trend was observed in the absolute number of snakebites over time averaging 504 reports per year . However, the bacterial infections are often secondary complications of wounds to animal bites, and it has been determined that pathogenic microorganisms responsible for infection are also present in the oral flora of the biting animal [9, 10].
It has been established that the ingested diet and its oral flora directly influence the oral microbiota of the snakes. It has been proposed that cloacal flora of the prey animals can be found in the oral cavity of the snakes, due to the prey defecating by the time it is ingested [9, 11]. Despite the influence of associations of bacteria and snakes and the influence of these bacteria on humans, there are few studies on the characterization and distribution of these microorganisms . However, some bacterial distributions, including some Gram-positive bacteria such as Staphylococcus sp., have been confirmed in snakes biota. They are predominant in the oral cavities of healthy snakes but Gram-negative bacteria such as Pseudomonas aeruginosa, Providencia rettgeri, and Pseudomonas maltophilia (currently Stenotrophomonas maltophilia) are predominant in the oral cavities of snakes with stomatitis [12, 13]. Other members belonging to the family Enterobacteriaceae can cause respiratory diseases in humans . Also some species of the genus Stenotrophomonas sp., for example, S. maltophilia, may induce diseases such as endocarditis, sepsis, meningitis, peritonitis, soft tissue infections, and wounds .
The aim of this study is to identify, characterize, and report the diversity of the bacterial community in the oral and cloacal cavities of venomous and nonvenomous snakes found in wildlife into the rainforest of central volcanic mountain range, Costa Rica.
2. Material and Methods
2.1. Area of Study
The Quebrada González sector forms part of the vast Braulio Carrillo National Park located in 10°09′39.88′′N y 83°56′13.97′′O. The forest located in the area is montane rainforest transitioning to tropical moist basal. It has been registered up to 6375,5 mm of annual precipitation and an average temperature of 24°C. On the other hand, the site’s average elevation is m and has strong inclines in most of its area . The forest composition varies from secondary to mature forests, including open areas formed by the Sucio river [15–17]. Also present are various important tributaries like Quebrada González that have a constant flow throughout the year, making the water source abundant in the sector [18, 19].
2.2. Sample Collection
The snakes were captured between August and November, 2014. On each field trip, sampling took place in the morning (7 a.m.–11 a.m.) and at night (7 p.m.–11 p.m.); since there are more active individuals [2, 19], search was conducted with an intensive search technique for a casual encounter , looking for individuals on the ground, on leaf litter, and on top of vegetation. Snakes were captured with the assistance of herpetological tongs and identified to a species level. A total of 120 swabs, oral and cloacal, were taken from 16 individuals of both Viperidae and Colubridae families. Samples were taken and immediately cultured on four different media at room temperature; Mannitol-salt agar (MSA), MacConkey agar (MCA), Salmonella-Shigella agar (SSA), and blood agar (BA). Cultures were taken to the laboratory on a 24- to 48-hour period; bacterial isolates were separated by morphology and Gram staining. Once grown and pure, cultures were inoculated on blood agar or trypticase soy agar for further processing. After 24 h, these isolates were taken to the Laboratorio de Bacteriología Médica, Facultad de Microbiología, Universidad de Costa Rica, to be identified and submitted to antibiotic susceptibility testing (AST) with the VITEK 2C platform (bioMérieux). To verify the identification provided on environmental isolates, molecular analyses were conducted on 27 isolates of different bacterial species.
2.3. Total DNA Extraction and PCR
Total genomic extraction was performed of bacterial pellets after strong centrifugation using STES buffer (0.2 M Tris-HCL, 0.5 M NaCl, 0.01 M EDTA, 1% SDS) and standard phenol/chloroform extraction method was performed . Specific 16S rDNA PCR-mediated amplification for bacterial taxonomy was executed with the following primers: 5′-AGAGTTTGATCMTGGCTCAG-3′ and 5′-GTTACCTTGTTACGACTT-3′ . Polymerase chain reactions were arranged at a 20 μl final volume with PCR Master Mix (2x) (Thermo Scientific®), 0.3 μM forward and reverse primer, and 100 ng of bacterial genomic DNA template. Thermocycling parameters for the gene fragment amplification consisted of initial denaturalization at 95°C for 5 min, followed by 36 cycles of denaturalization (95°C, 45 s), annealing (58–62°C, 1 min, 30 s), extension (72°C, 1 min, 15 s), and final extension step at 72°C for 7 min. PCR reactions were conducted on a thermal cycler (Proflex PCR System; Applied Biosystems, Life Technologies, USA). Amplicons were visualized by agarose gel electrophoresis (1.5%) in TBE 1x (Tris-base, boric acid, EDTA, pH 8), stained with GelRed® (Biotium). GeneRuler 1 kb plus DNA Ladder (Thermo Scientific) was used as size marker. Molecular biology grade water (Ambion®) was used as negative control.
2.4. Sequencing and Bioinformatics Analysis
PCR products were purified by isopropanol precipitation and quantified with a NanoDrop 2000 spectrophotometer (Thermo Scientific) and used for direct DNA sequencing. Partial gene fragments of 16S rRNA were sequenced, using the same amplification primer (BigDye Terminator® V3.1, Applied Biosystems), according to manufacturer’s instructions. The resulting products were purified with the Xterminator Kit (Applied Biosystems) and then run on DNA multicapillary sequencer (Model 3130, Applied Biosystems) at the Laboratorio de Análisis Genómico, Escuela de Ciencias Biológicas, Universidad Nacional, Costa Rica. Recovered sequences were edited using Geneious® R9 version (Biomatters Ltda), analyzed with BLASTn algorithm  at the NCBI (http://www.ncbi.nlm.nih.gov/blast) with the 16S ribosomal DNA sequences (Bacteria and Archaea) database, and compared with other previously published sequences. On the other hand, all bacterial 16S ribosomal DNA sequences obtained were compared with sequences of Ribosomal Database Project (RDP) database using the Seq Match algorithm, parameter S_ab score (http://rdp.cme.msu.edu/) for sequence similarities searches to confirm bacterial identity . Our nucleotide sequence data for 16S rRNA gene was deposited in GenBank (https://www.ncbi.nlm.nih.gov/genbank/) under accession numbers KY963324 to KY963344.
Local sequences and ones obtained at GenBank database were dereplicated by USEARCH v7.0 software  through cluster fast command application (under a threshold identity 0.99000). Then, nonduplicates clusters sequences were aligned using MUSCLE algorithm  with default parameters. Phylogenetic tree was performed using maximum likelihood (ML) by raxmlGUI v.7.4.2 [27, 28] software through GTR-GAMMA substitution model and 1000 rapid bootstrap inferences. The consensus trees were visualized and edited in FigTree 1.4 program .
A total of 90 bacterial isolates (from 120 cloacal and oral swabs) were recovered from 16 individuals of several species including Bothrops asper, Bothriechis schlegelii, Leptodeira septentrionalis, Sibon longifrenis, Oxyrhopus petolarius, Oxybelis brevirostris, and Imantodes cenchoa. Overall 40 different bacterial species (12 families) were identified by VITEK approach from both oral and cloacal swabs (Table 1). Both Viperidae species, B. asper and B. schlegelii, isolates had the most different bacterial morphotype with 32 and 18, respectively, followed by S. longifrenis with 13, O. petolarius with 9, L. septentrionalis and I. cenchoa with 7, and finally O. brevirostris with 4 isolates (data not shown). About the distinctive colony phenotypes, 47 of the isolates were found in oral swabs and 43 on the cloacal swabs. From all the isolates identified with the VITEK platform, none are certainly exclusive from either oral or cloacal swabs. However, the few isolates that were identified as a unique bacterial species in either cavity were identified only once. Amongst these unique genera, we can find Bordetella, Salmonella, Elizabethkingia, Sphingomonas, and Rhizobium.
In the family Enterobacteriaceae, a general resistance pattern was found for ampicillin and cephalothin, being susceptible to these antibiotics E. coli and R. ornithinolytica, respectively. On the other hand, they were widely susceptible to various antibiotics: PpC/Tzba, Cfa, Cftz, Cfe, Imi, Mer, Ami, Gen, and Cip2. The only exception is H. alvei showing resistance to the combination of PpC/Tzba. The second family with more representatives in our AST was Staphylococcaceae. It was widely susceptible to most of the antibiotics; however, S. saprophyticus and S. warneri were the only species with resistance to antibiotics. Additionally, several bacterial isolates identified as opportunistic pathogens show resistance to different antibiotics, for example, Aeromonas hydrophila (Amp and Amp/Sbt), Achromobacter xylosoxidans (Amp/Sbt, Gen, Na, and Nit) Serratia marcescens (Cef and Nit), Elizabethkingia meningoseptica (Amp, Amp/Sbt, PpC/Tzba, Gen, and Nit), and Pseudomonas fluorescens (Amp, Amp/Sbt, Na, and Nit) (Table 2).
In the phylogenetic structure obtained for Gram-positive bacteria, we observe clustering of four families: Micrococcaceae, Paenibacillaceae, Bacillaceae, and Staphylococcaceae. On this tree, conflict between identification analyses is shown for isolates SlO2914 and LsO2847. For the Gram-negative bacteria phylogenetic tree, our sequences clustered majorly in three families: Xanthomonadaceae, Pseudomonadaceae, and Enterobacteriaceae. In this topology, we have more taxonomic inconsistencies, mainly on the Enterobacteria, concerning these isolates: BsO3054, SlO2981, SlC2883, SlO2982, BaO2749, and LsC2975. However, more than 65 percent of the isolates analyzed with biochemical and molecular approach turned out in consistent identification at the genera level (Figure 1).
Differences in habitat, predation strategies, and the type of prey can provide an explanation for the high variation in bacterial flora . A marked trend on cloacal and oral isolates is not very well defined in our results. A factor that could influence the bacterial composition on oral or cloacal cavities is feeding habits. At the time of sampling, it is not known how recent has the snake eaten, which could explain why no differences on the number of isolates between terrestrial and arborous species were found. At the same time, it explains the lack of significant difference on oral and cloacal isolates. Another factor to consider is that snakes are very active and most species are not confined to a certain habitat .
Snake bites have a high rate of infection because of Gram-negative bacteria . This is due to their eating habits, where the prey head is ingested first, leaving a colonization of fecal flora on the oral cavity. This also could explain the higher amount of enterobacterial isolates found in the mouth of the individuals sampled.
Providencia sp. was found in the oral cavity of captive snakes from Costa Rica . Another study on Bothrops jararaca reported several species of bacteria from the oral cavity including Providencia rettgeri, Staphylococcus aureus, Salmonella typhimurium, Citrobacter sp., and Morganella morganii . This finding coincided with our study, except that we found the last three genera on the cloaca not in the mouth. On a study carried out by Ferreira Junior et al. (2009) , they indicate the presence of Salmonella enterica and M. morganii in the oral cavity of rattlesnakes, and also Citrobacter freundii was found in the cloaca. In nonvenomous snakes, such as Python regius and Clelia scyntalina, Serratia marcescens, M. morganii, and C. freundii and other species in the oral cavity were identified . On the other hand, Elaphe quatuorlineata (Colubridae) sampled at their natural habitats have shown bacterial isolates mainly of the genera Serratia, Stenotrophomonas, Escherichia, Aeromonas, Pseudomonas, Staphylococcus, and Bacillus .
Inconsistencies in bacterial identification between 16S rRNA sequencing and biochemical analyses conducted on the VITEK platform could be due to several factors. On a clinical study, 92% identity fidelity with a 16S sequencing approach was obtained, while VITEK only resolved 52% of the samples . In our case, some isolates could be difficult to identify due to lack of entries in the database. However, in almost all of the samples, percentages of identification from VITEK are above 90%. Another factor that could be interfering is the lack of primer match suitable sites on the 16S rRNA for bacterial species level identification ; also the primers used (27f and 1492r) are widely known universal primers. This leads to a possible systematic underrepresentation of the matching phylogenetic group due to a difference in nucleotides .
Bacteria isolated from snakes on a zoo, such as Citrobacter sp., Enterobacter sp., Escherichia coli, Hafnia alvei, Morganella morganii, Proteus sp., Stenotrophomonas maltophilia, and Pseudomonas sp., could be opportunistic pathogens and generate nosocomial infections. Besides, Sphingomonas paucimobilis has been associated with infections of the oral mucosa of humans . On the other hand, pathogens like Enterococcus faecalis, Salmonella arizonae, and Staphylococcus lentus can generate zoonosis . Similar bacterial genera were found compared to our results, where predominantly Staphylococcus, Pseudomonas, and Enterobacter match our findings .
Important to notice is the presence of M. morganii, a pathogen highly involved in abscess generation [30, 42]. The several species of Staphylococcus found can generate local infections and have been isolated in clinical cases . Yokenella regensburgei has been known to generate septicemias from soft tissue infections, especially for immunocompromised hosts . The capacity of Aeromonas hydrophila is well known to cause severe infections after snakebites . Another species identified was Raoultella ornithinolytica, a poorly described pathogen with rare cases of infection, with a high mortality rate reported (20%). This pathogen can produce bacteremia, skin infections, and respiratory infections .
Finally, Elizabethkingia meningoseptica was identified, an opportunistic pathogen that could have serious consequences on humans, with a reported 24% mortality rate over 118 patients . Although it was found on a nonvenomous species, it is fairly commonly distributed . This pathogen has been previously isolated in dead amphibians with cataracts and showed severe consequences to the host .
The vast majority of isolates showed antibiotic sensitivity patterns typical of wild, nonexposed strains and several natural resistance mechanisms widely distributed in nature. Resistance patterns suggested natural mechanisms of antibiotic resistance, such as constitutive chromosomal AmpC beta-lactamases and cephalosporinases, common in genera such as Enterobacter, Citrobacter, Serratia, Proteus, Escherichia, and Morganella . Probable evidences of QNR protein and efflux pumps could be present in Enterobacteria and Pseudomonas strains, according to their resistance to nalidixic acid, but not to quinolones . Similarly, resistance mechanisms to erythromycin and tetracycline due to efflux pumps could be present in Gram-positive cocci isolates, as they are widespread [50, 51].
An important diversity of aerobic bacteria was isolated (40 different bacterial species) from oral and cloacal mucous membrane from wildlife snakes species. Also with similar findings, other studies looked at bacterial diversity in different reptiles like turtles  and Komodo dragons , corroborating our results. Even studies regarding fungal diversity  conclude that these findings should be considering in the clinical picture when treating these animal bites. Importantly, antibiotics most appropriate in the case of infection by these pathogens are reported as well as the resistance found in these wild strains.
In summary, to our knowledge herein, this is the first report of a survey that combines biochemical and molecular approaches that identifies aerobic bacterial communities isolated from free-living venomous and nonvenomous snakes from Costa Rican rainforests. We also obtained an antibiotic susceptibility test (AST) for bacterial clusters inhabiting the cavities of local serpents. Our results revealed that the majority of the 12 bacterial families could bring health complications after a snakebite.
Conflicts of Interest
The authors declare that there are no conflicts of interest regarding the publication of this paper.
The authors are very grateful to the group of colleagues working with snakes at Braulio Carrillo, especially Jonathan Vega, Daniel Ramírez, Alejandro Zuñiga, Mauricio de la O, and Wouter Baaijen, for their effort on collaborating with sampling. At the same time, the authors appreciate the vital support of all laboratories involved: Laboratory of Genomic Analyses (LAGEN), Laboratory of Biotechnology at National University, and the Laboratory of Medical Bacteriology, Faculty of Microbiology, University of Costa Rica. Finally, the authors appreciate all the work from laboratory staff, especially Abad Rodríguez and Silvia Mau who facilitated commodities when needed.
A. Solórzano, Serpientes de Costa Rica, Instituto Nacional de Biodiversidad, Santo Domingo de Heredia, Costa Rica, 2004.
E. Hansson, M. Sasa, K. Mattisson, A. Robles, and J. M. Gutiérrez, “Using geographical information systems to identify populations in need of improved accessibility to antivenom treatment for snakebite envenoming in Costa Rica,” PLoS Neglected Tropical Diseases, vol. 7, no. 1, Article ID e2009, 2013.View at: Publisher Site | Google Scholar
J. M. Gutiérrez, “Snakebite poisoning in Latin America and the Caribbean: an integral view from a regional perspective,” Boletin de Malariologia y Salud Ambiental, vol. 51, no. 1, pp. 1–16, 2011.View at: Google Scholar
G. Blandón, Flora Bacteriana Asociada a la Cavidad Bucal en Serpientes de la Familia Viperidae, Trabajo de Grado en Modalidad de Extensión, Universidad de Caldas, Manizales Centro de Investigación y Asesoría Ofidiológica. OPHIDIA, 2009.
J. Iqbal, M. Sagheer, N. Tabassum, R. Siddiqui, and N. A. Khan, “Culturable aerobic and facultative anaerobic intestinal bacterial flora of black cobra (Naja naja karachiensis) in Southern Pakistan,” ISRN Veterinary Science, vol. 2014, Article ID 878479, 5 pages, 2014.View at: Publisher Site | Google Scholar
Y. S. Jho, D. H. Park, J. H. Lee, and Y. S. Lyoo, “Aerobic bacteria from oral cavities and cloaca of snakes in a petting zoo,” Korean Journal of Veterinary Research, vol. 51, no. 3, pp. 243–247, 2011.View at: Google Scholar
S. Baron, “Pseudomonas,” in Medical Microbiology, B. H. Iglewsk, Ed., chapter 27, University of Texas Medical Branch at Galveston, Galveston, Tex, USA, 4th edition, 1996.View at: Google Scholar
P. Oviedo-Pérez and L. Fournier-Gutiérrez, “Caracterización de la avifauna del sector Quebrada González, Parque Nacional Braulio Carrillo, Costa Rica,” Brenesia, vol. 69, pp. 25–33, 2008.View at: Google Scholar
W. McDiarmid, Reptile Biodiversity: Standard Methods for Inventory and Monitoring, University of California Press, 2012.
W. J. Sutherland, Ed., Ecological Census Techniques: A Handbook, Cambridge University Press, 2006.
K. H. Wilson, R. B. Blitchington, and R. C. Greene, “Amplification of bacterial 16S ribosomal DNA with polymerase chain reaction,” Journal of Clinical Microbiology, vol. 28, pp. 1942–1946, 1990.View at: Google Scholar
A. Rambaut, FigTree v1.4 2012–2014: Tree Figure Drawing Tool, http://tree.bio.ed.ac.uk/software/figtree.
K. C. Shek, K. L. Tsui, K. K. Lam et al., “Oral bacterial flora of the Chinese cobra (Naja atra) and bamboo pit viper (Trimeresurus albolabris) in Hong Kong SAR, China,” Hong Kong Medical Journal, vol. 15, no. 3, pp. 183–190, 2009.View at: Google Scholar
O. Arroyo, R. Bolaños, and G. Muñoz, “The bacterial flora of venoms and mouth cavities of Costa Rican snakes,” Bulletin of the Pan American Health Organization, vol. 14, no. 3, pp. 280–285, 1980.View at: Google Scholar
M. T. Jorge, J. S. de Mendonça, L. A. Ribeiro, M. L. da Silva, E. J. Kusano, and C. L. Cordeiro, “Bacterial flora of the oral cavity, fangs and venom of Bothrops jararaca: possible source of infection at the site of bite,” Revista do Instituto de Medicina Tropical de Sao Paulo, vol. 32, no. 1, pp. 6–10, 1990.View at: Publisher Site | Google Scholar
M. Lukač, D. Horvatek Tomić, Z. Mandac, S. Mihoković, and E. Prukner-Radovčić, “Oral and cloacal aerobic bacterial and fungal flora of free-living four-lined snakes (Elaphe quatuorlineata) from Croatia,” Veterinarski Arhiv, vol. 87, no. 3, pp. 351–361, 2017.View at: Google Scholar
P. P. Bosshard, R. Zbinden, S. Abels, B. Böddinghaus, M. Altwegg, and E. C. Böttger, “16S rRNA gene sequencing versus the API 20 NE system and the VITEK 2 ID-GNB card for identification of nonfermenting Gram-negative bacteria in the clinical laboratory,” Journal of Clinical Microbiology, vol. 44, no. 4, pp. 1359–1366, 2006.View at: Publisher Site | Google Scholar
Y.-C. Chiang, C.-Y. Yang, C. Li, Y.-C. Ho, C.-K. Lin, and H.-Y. Tsen, “Identification of Bacillus spp., Escherichia coli, Salmonella spp., Staphylococcus spp. and Vibrio spp. with 16S ribosomal DNA-based oligonucleotide array hybridization,” International Journal of Food Microbiology, vol. 107, no. 2, pp. 131–137, 2006.View at: Publisher Site | Google Scholar
M. S. Hsu, C. H. Liao, Y. T. Huang et al., “Clinical features, antimicrobial susceptibilities, and outcomes of Elizabethkingia meningoseptica (Chryseobacterium meningosepticum) bacteremia at a medical center in Taiwan, 1999–2006,” European Journal of Clinical Microbiology and Infectious Diseases, vol. 30, no. 10, pp. 1271–1278, 2011.View at: Publisher Site | Google Scholar
Z.-Y. Xie, Y.-C. Zhou, S.-F. Wang et al., “First isolation and identification of Elizabethkingia meningoseptica from cultured tiger frog, Rana tigerina rugulosa,” Veterinary Microbiology, vol. 138, no. 1, pp. 140–144, 2009.View at: Google Scholar
A. Hernández, M. B. Sánchez, and J. L. Martínez, “Quinolone resistance: much more than predicted,” Frontiers in Microbiology, vol. 2, p. 22, 2011.View at: Google Scholar
J. C. M. Junior, M. Marinho, C. V. Táparo, J. B. da Costa, and H. L. T. Dias, “Enterobacterias en tortugas silvestres y cautivas del Amazonas, Podocnemis expansa (Testudines: Podocnemididae),” Revista de Biología Tropical, vol. 63, no. 4, pp. 1083–1089, 2015.View at: Google Scholar
E. J. C. Goldstein, K. L. Tyrrell, D. M. Citron et al., “Anaerobic and aerobic bacteriology of the saliva and gingiva from 16 captive Komodo dragons (Varanus Komodoensis): New implications for the bacteria as venom model,” Journal of Zoo and Wildlife Medicine, vol. 44, no. 2, pp. 262–272, 2013.View at: Publisher Site | Google Scholar