SciELO - Scientific Electronic Library Online

 
vol.36Notes on Lagothrix flavicauda (Primates: Atelidae): oldest known specimen and the importance of the revisions of museum specimensMortality of primates due to roads and power lines in two forest patches in Bangladesh author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

Share


Zoologia (Curitiba)

Print version ISSN 1984-4670On-line version ISSN 1984-4689

Zoologia (Curitiba) vol.36  Curitiba  2019  Epub Oct 21, 2019

https://doi.org/10.3897/zoologia.36.e29587 

SHORT COMMUNICATION

Parasites in feces of the endemic rattlesnake, Crotalus triseriatus (Serpentes: Viperidae), from Mexican highlands

Leroy Soria-Díaz1 
http://orcid.org/0000-0002-2412-3211

Jaime Luis Rábago-Castro2 
http://orcid.org/0000-0002-0618-0490

Hublester Domínguez-Vega3 
http://orcid.org/0000-0002-2862-0872

Yuriana Gómez-Ortiz3 
http://orcid.org/0000-0002-1737-3941

Javier Manjarrez4 
http://orcid.org/0000-0003-3053-3257

Lorena Garrido-Olvera1  * 
http://orcid.org/0000-0001-8414-4519

1Instituto de Ecología Aplicada, Universidad Autónoma de Tamaulipas. División del Golfo 356, La Libertad, 87019, Ciudad Victoria, Tamaulipas, Mexico.

2Facultad de Medicina Veterinaria y Zootecnia, Universidad Autónoma de Tamaulipas. Carretera Victoria-Mante km 5, 87000, Ciudad Victoria, Tamaulipas, Mexico.

3División de Desarrollo Sustentable, Universidad Intercultural del Estado de México. Libramiento Francisco Villa SN, 50640, San Felipe del Progreso, Estado de México, Mexico.

4Centro de Investigación en Recursos Bióticos, Facultad de Ciencias, Universidad Autónoma del Estado de México. Instituto Literario 100, 50000, Toluca, Estado de México, Mexico.


ABSTRACT

There are few studies about parasitic infections in Crotalus triseriatus (Wagler, 1830), an endemic rattlesnake from the highlands of central Mexico. This species occupies several habitats, from conserved forested regions to heavily impacted landscapes. To increase the parasitological knowledge of this reptile species without impacting populations, we obtained fecal samples of 16 rattlesnakes between 2012 and 2014 from Toluca Valley, Mexico. By using flotation technique, we found oocysts of Eimeria sp. and eggs of Capillariidae sp. The most frequent parasite was Eimeria sp. (62.5%). This study provides the first records of occurrence of parasites in reptilian feces from Mexico. Our results may be important for wildlife conservation purposes, for example, they could indicate of the population health of this species during processes of translocation.

KEY WORDS: Coccidia; Mexico; Nematoda; reptile; urban wildlife

Reptiles are hosts of a wide variety of protozoan and metazoan parasites (Wilson and Carpenter 1996). Most of these parasites have been recorded through necropsies of specimens, although the diagnosis could be achieved by revealing parasitic elements in feces (e.g., eggs, larvae, oocysts). Even though, the latter non-invasive method only allows detecting intestinal parasites, may be useful for conservation projects, which involve knowing the health status of a reptile population in wildlife (Jorge et al. 2013).

In Mexico, 864 reptile species have been recorded (i.e., 8.7% of the reptiles of the world), of which 57% are endemic (Flores-Villela and García-Vazquez 2014). However, the inventory of their parasites is far from complete, since only a few more than 200 Mexican reptile species have been recorded as hosts of helminths, acari and crustaceans (Paredes-León et al. 2008).

Mexico holds the highest species richness of rattlesnakes, with 42 species (Heimes 2016), but wild populations have declined due to direct hunting and habitat loss caused by the expansion of croplands and urban areas. Particularly, the Mexican dusky rattlesnake, Crotalus triseriatus (Wagler, 1830), is restricted to the Trans-Mexican Volcanic Belt, where occupies forested regions heavily impacted (Bryson et al. 2014). This species is considered in the category of “least concern” in the IUCN and it has not received any level of protection by Mexican government due probably to a lack of knowledge in demographic and ecological aspects (Bryson et al. 2014, Sunny et al. 2015).

Translocations have increased for wildlife conservation, including the herpetofauna. One concern associated with conservation translocations is that the released individuals may suffer from parasitic diseases resulting in establishment failure. However, infectious hazards may be mitigated when diseases and/or parasites of translocated species or species at the destination are known (Bobadilla Suarez et al. 2017). Unfortunately, for C. triseriatus little is known about its parasites (Paredes-León et al. 2008), even though this information is essential to know the population health of this species and potentially useful in future translocation processes of species from one population to another. Our objective was to investigate the occurrence of parasites in feces of C. triseriatus to increase parasitological knowledge without affecting wild populations.

This study was conducted in Toluca Valley located in the State of Mexico, a highly anthropized area and considered the fifth largest metropolis in Mexico, with 2.1 million inhabitants (SEDESOL, CONAPO, INEGI 2004). The region has a humid temperate climate, with an annual precipitation of 500-600 mm and a range of average annual temperature between 12 and 15 °C (García 2004, Gobierno del Estado de México 2012). The sampling sites were El Cerrillo located at 5.1 km north of metropolitan area of Toluca City (19°24’27”N; 99°41’40”W; 2615 masl) and the Sierra Morelos Park located on the edge of the metropolitan area of Toluca City (19°18’39”N; 99°41’33”W; 2630 masl).

To capture individuals of C. triseriatus and collect individual fecal samples, during 2012 to 2014 we made 24 monthly visits at each study site, where five observers simultaneously walked five linear transects of 800 m long and separated by 300 m in a schedule of 09:00 am-13:00 pm. We capture the rattlesnakes with herpetological hooks and once subjected, we recorded total length (snout-vent length) in centimeters and weight in grams only with descriptive purposes. After we obtained fecal samples of each specimen place them in Eppendorf tubes and we released the rattlesnakes at their capture sites.

Each fecal sample was conserved in 70% alcohol and examined in the laboratory using the flotation technique (Bowman et al. 2004). Approximately 0.5 g of each sample was macerated and mixed with 9.0 ml of 0.8% saline solution. Each homogenized sample was filtered and placed in a vial, which was centrifuged for three minutes at 1500 rpm. After centrifugation, the supernatant was discarded, and a saturated glucose solution was used to re-suspend the pellet. The suspension was centrifuged for five minutes at 1000 rpm and three subsamples of top part of the flotation were obtained and examined by light microscopy. Parasitic elements (i.e., eggs and oocysts) were counted in each subsample to obtain an average per sample and to determine the levels of infection according to Rodríguez-Vivas and Cob-Galera (2005). Eggs and oocysts were photographed and measured using a light microscope at 40 and 100X magnifications (Leica DFC 490) and identified in accordance with Mehlhorn et al. (1993) and Wolf et al. (2014).

A total 16 Mexican dusky rattlesnakes were caught, 6 in El Cerrillo with 46-66 cm (56.42 ± 6.56) and 71-270 g (190.17 ± 73.7), and 10 in Sierra Morelos Park with 43-67 cm (55.03 ± 7.47) and 70-350 g (202.78 ± 78.19). Ten of the 16 fecal samples showed the presence of parasitic elements: nematode eggs of Capillariidae sp. and coccidian oocysts of Eimeria sp., with total prevalence of 62.5% y 6.25%, respectively (Table 1, Figs 1-2). The most frequent parasite was Eimeria sp. with high infection levels in both localities. Only one double parasitic infection was found in El Cerrillo.

Figures 1-2 Parasitic elements in feces of Crotalus triseriatus from Mexico: (1) Egg of Capillariidae sp. with one larva (L), brown color, thick and rough wall (W), one operculum at each pole (Op), which are asymmetrical. (2) Sporulated oocyst of Eimeria sp., spheroidal type, rough outer wall (W), absence of micropyle, ovoid sporocysts (S). Scale bars: 10 µm. 

Table 1 Infection levels of parasitic elements in feces of Crotalus triseriatus from two localities in the State of Mexico, Mexico. Range of oocysts/eggs per gram of feces and infection levels slightly modified of Rodríguez-Vivas and Cob-Galera (2005): 2-9 very low (+), 8-18 Low (++), 20-30/10-15 Medium (+++), 32-50 High (++++). 

Localities Host Collection date Eimeria sp. Capillariidae sp.
ID Length (cm) Weight (g)
Sierra Morelos Park SMP1 43.0 70 May 26, 2012 + Negative
SMP2 57.0 233 July 12, 2012 Negative Negative
SMP3 63.0 250 September 15, 2012 Negative Negative
SMP4 59.0 212 September 15, 2012 +++ Negative
SMP5 53.0 Undetermined April 27, 2014 ++ Negative
SMP6 53.0 185 September 20, 2014 Negative Negative
SMP7 51.8 200 October 18, 2014 ++++ Negative
SMP8 45.0 125 October 18, 2014 ++++ Negative
SMP9 67.0 350 November 01, 2014 Negative Negative
SMP10 58.5 200 November 01, 2014 Negative Negative
El Cerrillo CE1 66.0 250 October 20, 2012 ++++ Negative
CE2 54.5 140 December 08, 2012 +++ +++
CE3 46.0 71 December 08, 2012 ++ Negative
CE4 55.0 200 August 30, 2014 + Negative
CE5 58.0 210 November 08, 2014 +++ Negative
CE6 59.0 270 November 08, 2014 Negative Negative

Knowledge about the parasites of Mexican rattlesnakes is still far from complete. For example, in Crotalus spp. only 21 taxa of metazoan parasites (1 Acanthocephala, 3 Cestoda, 9 Nematoda, 3 Acari, and 5 Crustacea) have been recorded through necropsies of bred or wild specimens (Table 2). Of them, Ophiotaenia perspicua La Rue, 1911, Kalicephalus inermis coronellae (Ortlepp, 1923), Ixobioides sp., and Ophionyssus natricis (Gervais, 1844) were recorded in C. triseriatus. Thus, findings of Capillariidae sp. and Eimeria sp. represent new host records and this study is the first on the parasites of wild reptilians in Mexico using fecal samples.

Table 2 Records of metazoan parasites for Crotalus spp. in Mexico. 

Parasite Stage Habitat Host State Reference
Cestoda
Mesocestoides sp. Tetratiridium Body cavity C. enyo (Cope, 1861) Baja California Sur Goldberg et al. (2003)
C. molossus Baird & Girard, 1853 Undetermined Goldberg and Bursey (1999)
C. pricei Van Denburgh, 1895
C. willardi Meek, 1905 Chihuahua, Sonora Goldberg and Bursey (2000)
Oochoristica sp. Adult Intestine C. basiliscus (Cope, 1864) Colima Paredes-León et al. (2008)
Ophiotaenia perspicua Adult Intestine C. cinerens Hidalgo Flores-Barroeta et al. (1961)
Acanthocephala
Oligacanthorhynchidae sp. Cystacanth Body cavity C. basiliscus Michoacán Goldberg et al. (2006)
C. enyo Baja California Sur Goldberg et al. (2003)
C. lepidus (Kennicott, 1861) Undetermined Goldberg and Bursey (1999)
C. tigris Kennicott, 1859
C. willardi Chihuahua, Sonora Goldberg and Bursey (2000)
Nematoda
Hastospiculum onchocercum Chitwood, 1932 Adult Stomach C. tzabcan Klauber, 1952 Quintana Roo Carbajal-Márquez et al. (2018)
Hexametra boddaertii (Baird, 1860) Adult Body cavity C. tzabcan Yucatán Carbajal-Márquez et al. (2018)
C. basiliscus Sinaloa Goldberg et al. (2006)
Kalicephalus inermis coronellae Adult Intestine C. pusillus Klauber, 1952 Michoacán Comroe (1948), Schad (1962)
C. triseriatus
Kalicephalus inermis macrovulvus (Caballero, 1954) Adult Intestine C. molossus Ciudad de México Goldberg and Bursey (1999)
Macdonaldius oschei Chabaud & Frank, 1961 Adult Post vena cava C. basiliscus Colima Telford (1965)
Ophidascaris labiatopapillosa Walton, 1927 Adult C. molossus Durango Klauber (1972)
Ozolaimus ctenosauri Caballero, 1938 Adult Intestine C. polystictus (Cope, 1865) Ciudad de México Caballero y Caballero (1939)
Physocephalus sp. Larva Mesentery C. mitchellii (Cope, 1861) Baja California Goldberg et al. (2013)
Travassosascaris araujoi (Schneider, 1866) Adult Liver C. tzabcan Quintana Roo Carbajal-Márquez et al. (2018)
Acari
Amblyomma dissimile Koch, 1844 Adult Body surface C. durissus Linnaeus, 1758 Guerrero Paredes-León et al. (2008)
Argasidae sp. Body surface C. viridis viridis (Rafinesque, 1818) Chihuahua Gatica-Colima et al. (2014)
Ixobioides sp. Adult Body surface C. triseriatus Ciudad de México Paredes-León et al. (2008)
Ophionyssus natricis Adult Body surface C. durissus Ciudad de México Paredes-León et al. (2008)
C. triseriatus
C. cerastes cercobombus Savage & Cliff, 1953 Nuevo León Rodríguez and Lazcano (1992)
C. lepidus lepidus (Kennicott, 1861)
C. atrox Baird & Girard, 1853 Puebla Paredes-León et al. (2008)
C. ravus Cope, 1865
Ornithodoros turicata (Dugès, 1876) Larva C. mitchellii Baja California Gutsche and Mutschmann (2011)
C. ruber Cope, 1892 Baja California Sur
Crustacea
Porocephalus basiliscus Riley & Self, 1979 Adult C. basiliscus Colima Riley and Self (1979)
Porocephalus crotali Humboldt, 1812 Adult C. atrox Nuevo León Peláez and Julia (1983)
C. basiliscus Colima Peláez and Julia (1983)
C. catalinensis Cliff, 1954 Santa Catalina Island, Baja California Sur Goldberg et al. (2003)
C. culminatus Klauber, 1952 Guerrero Pelaéz and Julia (1983)
C. durissus Tamaulipas Peláez and Julia (1983)
C. tzabcan Campeche, Quintana Roo Carbajal-Márquez et al. (2018)
Porocephalus tortugensis Riley and Self, 1979 Adult C. tortugensis Van Denburgh & Slevin, 1921 Tortuga Island-Baja California Sur Riley and Self (1979)
Raillietiella crotali Ali, Riley and Self, 1984 Adult Lung C. ruber Pond Island, Baja California Ali et al. (1984)
Raillietiella furcocercum (Diesing, 1836) Adult Lung C. atrox tortugensis Baird & Girard, 1853 Tortuga Island-Baja California Sur Ali et al. (1984), Klauber (1972)

The eggs of Capillariidae sp. found in C. triseriatus were not identified at specific level, since capillariid eggs are morphologically almost identical even among species of different genera (see Moravec 1994). Therefore, we cannot know if the nematode is a parasite or a pseudoparasite for Mexican dusky rattlesnakes, i.e., a parasite of the rodents on which hosts feed (personal observation of hair follicles in all fecal samples). In this context, Fuehrer (2014) recognized that endo- and ectoparasites of potential prey animals can be recorded as transiting parasites in the intestinal tract of reptiles, for example eggs of Capillaria hepaticum (Bancroft, 1893), a parasite species in mammals, have been documented in fecal samples from reptiles fed with infected rodents. On the other, Šlapeta et al. (2018) pointed out that the nematodes of Capillaria (Zeder, 1800) are the only known trichurids affecting reptiles, infecting primarily the intestine and secondarily other organs as the liver and gonads. It is known that their life cycle is direct, unfortunately the life cycles of snakes capillarids have not been investigated (Anderson 2000).

An examination of fecal samples of captive reptiles, including specimens of Crotalus Linnaeus, 1758, from Campania region in southern Italy revealed the most frequent parasites were species of groups of Oxyurida, Rhabdias Stiles & Hassall, 1905, Kalicephalus Molin, 1861, Capillaria and Eimeriidae Minchin, 1903 (Rinaldi et al. 2012). Analysis of the fecal samples in the present work confirmed that capillariids and eimeriids are the most frequent parasites of the reptiles, but they did not show the presence of any of the helminths recorded of rattlesnakes in Mexico (Table 2).

The oocysts of Eimeria sp. were not identified at specific level, because we did not observe some taxonomic characteristics. But it is known that Eimeria Schneider, 1875 is the most numerous group of snake coccidian with more than 80 species, which differ in both the morphology of exogenous stages (oocysts) and in endogenous development (Modrý 2004). Most species of Eimeria inhabit the intestine of reptiles, which become infected after ingesting oocysts. Schizogony occurs in the epithelial lining of intestine, depending on parasite species. Oocysts are shed with the feces following gametogony. The pathologic effects of coccidian appear mild for most reptiles; however, more severe cases resulting in epithelial ulceration and fibrosis, and septicemia from the loss of epithelial integrity, may occur (Mitchell 2007).

Jorge et al. (2013) found the detectability of nematodes was significantly lower in feces than in the intestine of reptiles, suggesting a large number of fecal samples and temporal replication to increase the likelihood of detection of intestinal parasites. Undoubtedly, parasitological studies based solely on feces most probably underestimate the true species richness present in a given host population and/or locality. However, such studies may be important for wildlife conservation purposes mainly when the translocations are employed, since the released individuals or individuals within the destination ecosystem may suffer from parasitic disease linked to the translocation process (Bobadilla Suarez et al. 2017). Specifically, it has been shown the vulnerability of populations of C. triseriatus in the Toluca Valley, due to the proximity to urban areas (Sunny et al. 2015), therefore, a complete parasitological record would aid wellbeing of snakes by receiving appropriate treatment plan and/or quarantine procedures. That allow to move the rattlesnakes outside the urban area, without the danger of infecting other populations with any diseased.

ACKNOWLEDGEMENTS

We thank Cruz Armida Olmeda Espinoza for the processing of the samples as laboratory technician in Facultad de Medicina Veterinaria y Zootecnia of the Universidad Autónoma de Tamaulipas.

LITERATURE CITED

Ali JH, Riley J, Self JT (1984) A revision of the taxonomy of pentastomid parasites (genus Raillietiella Sambon, 1910) from American snakes and amphisbaenians. Systematic Parasitology 6: 87-97. https://doi.org/10.1007/BF02185516Links ]

Anderson RC (2000) Nematode parasites of vertebrates. Their development and transmission. Wallingford, CABI Publishing, 650 pp. [ Links ]

Bobadilla Suarez M, Ewen JG, Groombridge JJ, Beckmann K, Shotton J, Masters N, Hopkins T, Sainsbury AW (2017) Using qualitative disease risk analysis for herpetofauna conservation translocations transgressing ecological and geographical barriers. EcoHealth 14: S47-S60. https://doi.org/10.1007/s10393-015-1086-4Links ]

Bowman D, Lynn RC, Eberhard ML (2004) Georgis parasitología para veterinarios. Madrid, Elsevier, 453 pp. [ Links ]

Bryson RW Jr, Linkem CW, Dorcas ME, Lathrop A, Jones JM, Alvarado-Díaz J, Grünwald CI, Murphy RW (2014) Multilocus species delimitation in the Crotalus triseriatus species group (Serpentes: Viperidae: Crotalinae), with the description of two new species. Zootaxa 3826: 475-496. https://doi.org/10.11646/zootaxa.3826.3.3Links ]

Caballero y Caballero E (1939) Nemátodos de los reptiles de México III. Anales del Instituto de Biología, Universidad Nacional Autónoma de México, Serie Zoología 10: 73-82. [ Links ]

Carbajal-Márquez RA, González-Solís D, Cedeño-Vázquez JR (2018) Endoparasites of Crotalus tzabcan (Serpentes: Viperidae), with a checklist in rattlesnakes. Journal of Parasitic Diseases 42: 303-314. https://doi.org/10.1007/s12639-018-1001-3Links ]

Comroe DB (1948) Kalicephalus conoidus, n. sp. (Strongylata), a nematode from the rattlesnake Crotalus triseriatus. Transactions of the American Microscopical Society 67: 280-284. https://www.jstor.org/stable/3223195Links ]

Flores-Barroeta L, Hidalgo-Escalante E, Montero-Gei F (1961) Céstodos de Vertebrados. VIII. Revista de Biología Tropical 9: 187-207. [ Links ]

Flores-Villela O, García-Vázquez UO (2014) Biodiversity of reptiles in Mexico. Revista Mexicana de Biodiversidad 85: S467-S475. https://doi.org/10.7550/rmb.43236Links ]

Fuehrer HP (2014) An overview of the host spectrum and distribution of Calodium hepaticum (syn. Capillaria hepatica): part 2 - Mammalia (excluding Muroidea). Parasitology Research 113: 641-651. https://doi.org/10.1007/s00436-013-3692-9Links ]

García E (2004) Modificaciones al sistema de clasificación climática de Köppen. Serie Libros Núm. 6. Instituto de Geografía, Mexico, Universidad Nacional Autónoma de México, 90 pp. [ Links ]

Gatica-Colima A, Macias-Rodríguez EF, Paredes-León R (2014) Crotalus viridis viridis (Prairie Rattlesnake) Ectoparasites. Herpetological Review 45: 143-144. [ Links ]

Gobierno del Estado de México (2012) Programa para Mejorar la Calidad del Aire del Valle de Toluca (2012-2017). Mexico, Gobierno del Estado de México, Secretaría del Medio Ambiente, 105 pp. [ Links ]

Goldberg SR, Bursey CR (1999) Crotalus lepidus (Rock Rattlesnake), Crotalus molossus (Blacktail Rattlesnake), Crotalus pricei (Twin-spotted Rattlesnake), Crotalus tigris (Tiger Rattlesnake). Endoparasites. Herpetological Review 30: 44-45. [ Links ]

Goldberg SR, Bursey CR (2000) Crotalus mitchellii (Speckled rattlesnake) and Crotalus willardi (Ridgenose rattlesnake). Endoparasites. Herpetological Review 31: 104. [ Links ]

Goldberg SR, Bursey CR, Beaman KR (2003) Crotalus enyo (Baja California Rattlesnake). Endoparasites. Herpetological Review 34: 64-65. [ Links ]

Goldberg SR, Bursey CR, Beaman KR, Dugan EA (2006) Crotalus basiliscus (Mexican West Coast Rattlesnake). Endoparasites. Herpetological Review 37: 94. [ Links ]

Goldberg SR, Bursey CR, Glaudas X (2013) Helminths of the Speckled Rattlesnake, Crotalus mitchellii (Squamata: Viperidae). Western North American Naturalist 73: 533-535. https://doi.org/10.3398/064.073.0407Links ]

Gutsche A, Mutschmann F (2011) Crotalus mitchellIi (Speckled Rattlesnake) and Crotalus ruber (Red Diamond Rattlesnake). Ectoparasites. Herpetological Review 42: 287-288. [ Links ]

Heimes P (2016) Herpetofauna Mexicana. Frankfurt am Main, Edition Chimaira, vol. 1, 572 pp. [ Links ]

Jorge F, Carretero MA, Roca V, Poulin R, Perera A (2013) What you get is what they have? Detectability of intestinal parasites in reptiles using faeces. Parasitology Research 112: 4001-4007. https://doi.org/10.1007/s00436-013-3588-8Links ]

Klauber LM (1972) Rattlesnakes: their habits, life histories, and influence on mankind. Berkeley, University of California Press, 1533 pp. [ Links ]

Mehlhorn H, Düwel D, Raether W (1993) Manual de Parasitología Veterinaria. Bogotá, Grass-Iatros, 436 pp. [ Links ]

Mitchell MA (2007) Parasites of reptiles. In: Baker DG (Ed) Flynn’s parasites of laboratory animals. Iowa, Blackwell Publishing, 177-216. [ Links ]

Modrý D, Nečas P, Mazuch T, Kamler M (2004) Eimeria atheridis n. sp. (Apicomplexa: Eimeriidae), a new coccidium from the western bush viper Atheris chlorechis (Pel, 1851) from tropical Africa. Systematic Parasitology 59: 71-74. https://doi.org/10.1023/B:SYPA.0000038444.21384.93Links ]

Moravec F (1994) Parasitic Nematodes of Freshwater Fish of Europe. The Netherlands, Kluwer Academic Publishers, 473 pp. [ Links ]

Paredes-León R, García-Prieto L, Guzmán-Cornejo C, León-Règagnon V, Pérez TM (2008) Metazoan parasites of Mexican amphibians and reptiles. Zootaxa 1904: 1-166. http://www.realitat.com/websites/zoologia/zoo_08/tecnicos_s_853645/archivos/Metazoan%20parasites.pdfLinks ]

Peláez D, Juliá J (1983) Pentastómidos de México. I. Porocefalosis en serpientes. (Comunicación preliminar). (Pentastom.: Poroceph. y Reptilia: Squamata). Anales de la Escuela Nacional de Ciencias Biológicas 27: 29-37. [ Links ]

Riley J, Self JT (1979) On the systematics of the pentastomid genus Porocephalus (Humboldt, 1811) with descriptions of two new species. Systematic Parasitology 1: 25-42. https://doi.org/10.1007/BF00009772Links ]

Rinaldi L, Mihalca AD, Cirillo R, Maurelli MP, Montesano M, Capasso M, Cringoli G (2012) FLOTAC can detect parasitic and pseudoparasitic elements in reptiles. Experimental Parasitology 130: 282-284. https://doi.org/10.1016/j.exppara.2012.01.011Links ]

Rodríguez ML, Lazcano D (1992) Primer reporte de ácaro Ophionyssus natricis (Acarina: Macronyssidae) para México. The Southwestern Naturalist 37: 426. https://www.jstor.org/stable/3671798Links ]

Rodríguez-Vivas RI, Cob-Galera LA (2005) Técnicas diagnósticas en parasitología veterinaria. Mérida, Universidad Autónoma de Yucatán, 306 pp. [ Links ]

Schad GA (1962) Studies on the genus Kalicephalus (Nematoda: Diaphanocephalidae). II. A taxonomic revision of the genus Kalicephalus Molin, 1861. Canadian Journal of Zoology 40:1035-1165. https://doi.org/10.1139/z62-090Links ]

SEDESOL, CONAPO, INEGI (2004) Delimitación de las zonas metropolitanas de México. Mexico, Secretaría de Desarrollo Social, Consejo Nacional de Población, Instituto Nacional de Estadística, Geografía e Informática, 169 pp. [ Links ]

Šlapeta J, Modrý D, Johnson R (2018) Reptile parasitology in health and disease. In: Doneley B, Monks D, Johnson R, Carmel B (Eds) Reptile medicine and surgery in clinical practice. Sussex, Wiley Blackwell, West 425-439. [ Links ]

Sunny A, Monroy-Vilchis O, Zarco-González MM, Mendoza-Martínez GD, Martínez-Gómez D (2015) Genetic diversity and genetic structure of an endemic Mexican Dusky Rattlesnake (Crotalus triseriatus) in a highly modified agricultural landscape: implications for conservation. Genetica 143: 705-716. https://doi.org/10.1007/s10709-015-9868-8Links ]

Telford SR (1965) A study of filariasis in Mexican snakes. Japanese Journal of Experimental Medicine 35: 565-586. [ Links ]

Wilson SC, Carpenter JW (1996) Endoparasitic diseases of reptiles. Seminars in Avian and Exotic Pet Medicine 5: 64-74. https://doi.org/10.1016/S1055-937X(96)80019-3Links ]

Wolf D, Vrhovec M, Failing K, Rossier C, Hermosilla C, Pantchev N (2014) Diagnosis of gastrointestinal parasites in reptiles: comparison of two coprological methods. Acta Veterinaria Scandinavica 56: 44. https://doi.org/10.1186/s13028-014-0044-4 Links ]

Publication Notes

Available online: October 1, 2019

Zoobank Register: http://zoobank.org/63164075-3A27-4D5A-B86D-1C2EAFD0B5F0

Publisher: © 2019 Sociedade Brasileira de Zoologia. Published by Pensoft Publishers at https://zoologia.pensoft.net

Received: September 13, 2018; Accepted: August 17, 2019; Published: October 01, 2019

*Corresponding author: Lorena Garrido-Olvera (lolvera@docentes.uat.edu.mx)

Author Contributions:

LSD and LGO contributed to the original idea. LGO JLRC and LSD wrote the draft of the manuscript. LGO and JLRC conducted laboratory analysis. LSD, YGO, HDV and JM contributed to field samplingt and provided revisions on the manuscript.

Competing Interests:

The authors have declared that no competing interests exist.

Editorial responsibility:

Sionei R. Bonatto

Creative Commons License This is an open-access article distributed under the terms of the Creative Commons Attribution License