Correlation between endoscopic sex determination and gonad histology in pond sliders, Trachemys scripta (Reptilia: Testudines: Emydidae)

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Edinburgh Research Explorer Correlation between endoscopic sex determination and gonad histology in pond sliders, Trachemys scripta (Reptilia: Testudines: Emydidae) Citation for published version: Perpinan, D, Martinez-Silvestre, A, Bargallo, F, Di Giuseppe, M, Oros, J & Pereira Da Costa, T 2016, 'Correlation between endoscopic sex determination and gonad histology in pond sliders, Trachemys scripta (Reptilia: Testudines: Emydidae)' Acta Herpetologica, vol. 11, no. 1, pp. 91-94. DOI: 10.13128/Acta_Herpetol-16038 Digital Object Identifier (DOI): 10.13128/Acta_Herpetol-16038 Link: Link to publication record in Edinburgh Research Explorer Document Version: Publisher's PDF, also known as Version of record Published In: Acta Herpetologica General rights Copyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s) and / or other copyright owners and it is a condition of accessing these publications that users recognise and abide by the legal requirements associated with these rights. Take down policy The University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorer content complies with UK legislation. If you believe that the public display of this file breaches copyright please contact openaccess@ed.ac.uk providing details, and we will remove access to the work immediately and investigate your claim. Download date: 29. Dec. 2018

Acta Herpetologica 11(1): 91-94, 2016 DOI: 10.13128/Acta_Herpetol-16038 Correlation between endoscopic sex determination and gonad histology in pond sliders, Trachemys scripta (Reptilia: Testudines: Emydidae) David Perpiñán 1, Albert Martínez-Silvestre 2,3, Ferran Bargalló 3, Marco Di Giuseppe 4, Jorge Orós 5, Taiana Costa 6, * 1 Hospital for Small Animals, Royal (Dick) School of Veterinary Studies, University of Edinburgh. Easter Bush Campus, Midlothian EH25 9RG, Scotland, United Kingdom 2 CRARC, Centre de Recuperació d Amfibis i Rèptils de Catalunya, Masquefa 08783, Barcelona, Spain 3 Zoològic Badalona Veterinària, Conquesta 74, Badalona 08912, Barcelona, Spain 4 Centro Veterinario per Animali Esotici. Viale Regione Siciliana Sud-Est 422-426, 90129, Palermo, Italy. 5 Department of Morphology, School of Veterinary Science, Universidad de las Palmas de Gran Canaria. Arucas 35413, Las Palmas de Gran Canaria, Spain. 6 Division of Infection and Immunity, The Roslin Institute, University of Edinburgh. Easter Bush Campus, Midlothian EH25 9RG, Scotland, United Kingdom. *Corresponding author. E-mail: taiana.costa@roslin.ed.ac.uk Submitted on 2015, 18 th March; reviewed on 2015, 12 th November; accepted on 2015, 4 th December Editor: Sandra Hochscheid Abstract. Coelioscopy has been proven to be a valuable technique to determine the sex of juvenile chelonians. However, there is a disagreement regarding the proper way to identify testes and ovaries, which is a direct consequence of the lack of studies correlating the results of endoscopic examination with the histology of the gonad. In this blinded study we assessed two methods of sex determination in juvenile pond sliders (Trachemys scripta) using endoscopy: via coelioscopy, with visualization of the gonads, and via cloacoscopy, with visualization of phallus/clitoris; we then compared the results of these procedures with the histology of the gonad. The results of gonad histology correlated 100% with the results from coelioscopic examination, but only 57.77% of the results obtained by cloacoscopy were accurate. Using cloacoscopy, 83.33% of males and 38.46% of females were misdiagnosed. Sex determination of juvenile pond sliders was considered accurate when coelioscopy was used, but inaccurate when cloacoscopy with identification of phallus/clitoris was attempted. Keywords. Reptiles, turtles, chelonians, anatomy, diagnostic imaging, endoscopy, sex determination. Most chelonians are long-lived animals where external/secondary sexual characteristics are only evident after several years of age (Mushinsky et al., 1994). For this reason, coelioscopy has been proven to be a valuable technique to determine the sex of juvenile chelonians before they show secondary sexual characteristics (Kuchling, 2006; Hernandez-Divers et al., 2009; Kuchling and Griffiths, 2012). However, there has been a disagreement about the proper identification of testes and ovaries in juvenile chelonians using coelioscopy (Hernandez-Divers et al., 2009; Kuchling, 2009; Innis 2012). This controversy arose from the lack of studies correlating the results of sex determination using endoscopic images with the histology of the gonad. We therefore designed a study to correlate the results of endoscopic sex determination in juvenile pond sliders (Trachemys scripta) via coelioscopy (with visual inspection of the gonad) and cloacoscopy (with visual inspection of the phallus/clitoris) with the result of postmortem histological examination of the gonads. ISSN 1827-9635 (print) ISSN 1827-9643 (online) Firenze University Press www.fupress.com/ah

92 David Perpiñán et alii Fifteen juvenile pond sliders, weighing 93-164 g (mean = 124.5 g) and measuring 7.5-9.9 cm (mean = 8.74 cm) of straight carapace length, were captured near the city of Barcelona (NE Spain) under the pest control project (permit number 002363 from the Departament de Medi Ambient of the Generalitat de Catalunya). Animals were maintained at 22 C and fastened for 48 hours prior to the procedures. Each animal was anaesthetised with alfaxalone (Alfaxan, Vetoquinol, Spain) at 10 mg/ kg IV (subcarapacial vein) and injected with lidocaine SC (0.1 ml of a 1 mg/ml dilution) in the left prefemoral area. Coelioscopies and cloacoscopies were performed in each animal using a 2.7 mm, 30 o viewing rigid endoscope with a protective sheath and a videocamera (Karl Storz Endoscopia Ibérica SA, Madrid, Spain). Briefly, for coelioscopic examination a 3-mm skin incision was performed in the centre of the prefemoral fossa and access to the coelomic cavity was performed separating the associated muscles; the endoscope was then inserted into the coelom and 10-20 ml of sterile saline (NaCl 0.9%) was used to insufflate the coelomic cavity; the endoscope was directed dorsocaudally in order to inspect the reproductive system (Divers et al., 2009). For cloacoscopic examination, the endoscope was inserted through the cloaca and directed cranially; 10-15 ml of air was used to insufflate the cloaca to visualize phallus/clitoris located in the ventral aspect of the proctodeum (Spadola and Insacco, 2009; Selleri et al., 2013). Following the procedures, turtles were not allowed to recover and were euthanased with an overdose of intravenous sodium thiopental (2 ml of Tiobarbital Braun, Braun, Spain). Necropsies were performed immediately after death and the gonads were collected, fixed in 10% neutral buffered formalin, processed routinely for histology, stained with haematoxylin and eosin and assessed under light microscopy. This was a blinded study, where the veterinarian performing coelioscopies (DP) and the veterinarian performing cloacoscopies (AM) did not know the results generated by each other; in addition, the pathologist (TC) did not know the results from coelioscopies and cloacoscopies. Furthermore, videos of the endoscopic procedures (both coelioscopies and cloacoscopies) were recorded and submitted to two independent veterinarians with experience in chelonian anatomy (JO and MG) for additional blinded evaluations. The Fleiss kappa statistical measure was used for assessing the reliability of agreement between observers (Geertzen, 2012). Histology was considered the gold standard for gonad identification. Results are shown in Table 1. Gonad histology revealed that 13 turtles were female and two turtles were male. Results from coelioscopies correlated 100% with the results from gonad histology, and the statistical analysis showed a perfect agreement (ϰ = 1) between observers. However, only 57.77% of the sexing results made via cloacoscopy were accurate, and the statistical analysis showed a poor agreement (ϰ = -0.324) between observers. Using cloacoscopy, males were misdiagnosed as females in 83.33% of cases and females were misdiagnosed as males in 38.46% of cases. Table 1. Comparison of sex determination of 15 pond sliders (Trachemys scripta) using coelioscopy, cloacoscopy and gonad histology. Animal Gonad histology Celioscopy Cloacoscopy Observer 1 Observer 2 Observer 3 Observer 1 Observer 2 Observer 3 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15

Endoscopy in turtles 93 Fig. 1. Endoscopic images of ovary (A, B, C), testicle (D, E) and clitoris (F) in pond sliders (Trachemys scripta). Ovary (Ov), oviduct (Du), intestines (In), testicle (Te), epididymis (Ep), vas deferens (Vd), kidney (Ki), proctodeum (Pr), clitoris (Cl), and accessory vesicles (Av). On coelioscopic examination, ovaries were long, irregular and translucent organs. They were loosely attached to the dorsal coelomic wall by long and loose ovarian ligaments on both poles of the organ (Fig. 1A). Ovarian previtellogenic follicles varied in density, size and appearance, from a few small, white to yellow round follicles embedded in the organ, to multiple prominent large yellow round follicles distributed through most of the parenchyma (Fig. 1B). The different features of the ovarian follicles were not associated with body weight or carapace length. Dark pigment and small vessels were appreciated in some ovaries (Fig. 1C). Adrenal glands were not always easily identified. The oviduct was a white, straight and tubular structure with small blood vessels on its surface. It ran parallel to and extended further cranially and caudally than the ovary, associated with the ovarian ligaments. It was observed either dorsally or ventrally to the ovary; occasionally, it was dorsal in the cranial part of the ovary and ventral in the caudal part. The diameter of the oviduct was variable, and sometimes it had a similar diameter as the ovary. Testes were slightly oval, white to yellow, and had a net of blood vessels on the surface of the organ, irradiating from the area of the mesorchium (Fig. 1D). The testicle was closely attached to the coelomic wall and only tight and short ligaments were visible on both poles of the organ (Fig. 1E). A black and relatively diffuse structure (believed to be the epididymis) was closely associated with the mesenteric surface of the testicle. Melanic spots were not found on the surface of testes. Vas deferens was only seen in one animal (50% of males) as a thin and white straight tubular structure, only visible arising from the caudal aspect of the testicle. On cloacoscopic examination, phallus and clitoris had an identical appearance; they were heart-shaped structures (with the tip of the heart pointing caudally) situated on the ventral aspect of the proctodeum. Both proctodeum and phallus/clitoris were pigmented (Fig. 1F). Appropriate description of gonads and associated structures are provided in the present article. It should be noted that interspecific differences in gonad mor-

94 David Perpiñán et alii phology may exist; for example, images provided by Hernandez-Divers et al. (2009) showed melanic testes in Chinese box turtles (Cuora flavomarginata); testes with pink and orange colours have also been described in chelonians (Kuchling, 2006); testes from Aldabra tortoises (Aldabrachelys gigantea) in a study by Kuchling and Griffiths (2012) were much more elongated that the ones observed in the present study with pond sliders. We observed variation in density, size, colour and shape of ovarian follicles in pond turtles of similar size and body weight. It has been described that follicles become more yellow, larger and more abundant as the animal ages (Kuchling, 2006). In our study, sex identification of juvenile pond sliders by visualization of phallus/clitoris via cloacoscopy was unreliable and therefore this method is not recommended for sex identification. However, visualization of gonads via coelioscopy was 100% accurate at determining the sex of juvenile pond sliders and, therefore, it is recommended for sexing chelonians whose secondary sexual characteristics are not evident. The small number of males included in our study should be considered a potential source of bias. A different endoscopic technique through cloacoscopy and access to the urinary bladder or accessory urinary vesicles has been described for sex determination in adult European freshwater turtles (Emys orbicularis) (Spadola and Insacco, 2009) and juvenile Mediterranean tortoises (Testudo hermanni) (Selleri et al., 2013). This technique offers the advantage of being less invasive than coelioscopy, and further studies will need to assess efficacy and safety in juvenile pond sliders or other chelonian species. ACKNOWLEDGMENTS We would like to thank Jordi Grífols from Zoològic Badalona Veterinària for his support to this study. REFERENCES Divers, S.J., Stahl, S.J., Camus, A. (2010): Evaluation of diagnostic coelioscopy including liver and kidney biopsy in freshwater turtles (Trachemys scripta). J. Zoo. Wild. Med. 41: 677-687. Geertzen, J. (2012): Inter-rater agreement with multiple raters and variables. Retrieved November 7, 2015, from https://nlp-ml.io/jg/software/ira/ Hernandez-Divers, S.J., Stahl, S.J., Farrell, R. (2009): An endoscopic method for identifying sex of hatchling Chinese box turtles and comparison of general versus local anesthesia for coelioscopy. J. Am. Vet. Med. Assoc. 234: 800-804. Innis, C.J. (2012): Testes morphology in Cuora flavomarginata: a response to Kuchling and Griffiths (2012; Chelonian Conservation and Biology 11[1]). Chelonian Conserv. Biol. 11: 273-274. Kuchling, G. (2006): Endoscopic sex determination in juvenile freshwater turtles, Erymnochelys madagascariensis: morphology of gonads and accessory ducts. Chelonian Conserv. Biol 5: 67-73. Kuchling, G. (2009): Differences among studies on sex identification on hatchling turtles. J. Am. Vet. Med. Assoc 235: 932-933 (letter answered by Hernandez- Divers and Stahl). Kuchling, G., Griffiths, O. (2012): Endoscopic imaging of gonads, sex ratios, and occurrence of intersexes in juvenile captive-bred Aldabra tortoises. Chelonian Conserv. Biol. 11: 91-96. Mushinsky, H.R., Wilson, D.S., McCoy, E.D. (1994): Growth and sexual dimorphism of Gopherus polyphemus in central Florida. Herpetologica 50: 119-128. Selleri, P., Di Girolamo, N., Melidone, R. (2013): Cystoscopic sex identification of posthatchling chelonians. J. Am. Vet. Med. Assoc. 242: 1744-1750. Spadola, F., Insacco, G. (2009): Endoscopy of cloaca in 51 Emys trinacris (Fritz et al., 2005): morphological and diagnostic study. Acta Herpetol. 4: 73-81.