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Neoctangium travassosi (Digenea: Microscaphidiidae) in sea turtles from South America

[Neoctangium travassosi (Digenea: Microscaphidiidae) em tartarugas marinhas da América do Sul]

ABSTRACT

Sea turtles are endangered animals that present cosmopolitan distribution. Anthropic actions have been considered important causes for the reduction of sea turtle population, but natural aspects such as parasitism may also contribute to their decline. This study aimed to report the occurrence of parasites in stranded dead sea turtles found in an area known as Potiguar Basin, northeastern Brazil, from 2010 to 2019. They were identified and classified according to the carapace length. At post-mortem analyses all organs were examined, parasites collected and morphologically identified. Ecological parasitic indexes as prevalence (P), mean intensity (MI) and mean abundance (MA) were calculated. A total of 80 Chelonia mydas and 5 Eretmochelys imbricata were assessed. Neoctangium travassosi was detected in both species presenting P = 20%, MI = 4.19 and MA = 0.84 for C. mydas and P = 60%, MI = 1.67 and MA = 1.0 for E. imbricata. This is the first report of N. travassosi parasitizing E. imbricata in South America. Finally, the retrieval of these parasites is a warning regarding the need for further studies to assess the impact of this parasitism on the health and conservation of sea turtles.

Keywords:
helminthes; marine turtles; parasitic indexes; South America

RESUMO

As tartarugas marinhas são animais ameaçados de extinção que apresentam distribuição cosmopolita. Ações antrópicas têm sido consideradas causas importantes para a redução da população de tartarugas marinhas, mas aspectos naturais, como o parasitismo, também, podem contribuir para o seu declínio. Este estudo objetivou relatar a ocorrência de parasitos em tartarugas marinhas, encalhadas mortas, encontradas em uma área conhecida como Bacia Potiguar, nordeste do Brasil, de 2010 a 2019. Essas foram identificadas e classificadas de acordo com o comprimento da carapaça. Nas análises post mortem, todos os órgãos foram examinados, e os parasitos coletados e identificados morfologicamente. Foram calculados índices parasitários ecológicos, como prevalência (P), intensidade média (IM) e abundância média (AM). Um total de 80 Chelonia mydas e cinco Eretmochelys imbricata foi estudado. Neoctangium travassosi foi detectado em ambas as espécies, apresentando P = 20%, MI = 4,19 e MA = 0,84 para C. mydas e P = 60%, IM = 1,67 e AM = 1,0 para E. imbricata. Este é o primeiro relato de N. travassossi parasitando E. imbricata na América do Sul. Conclui-se que a recuperação desses parasitos soa como um alerta para a necessidade de mais estudos para avaliar o impacto desse parasitismo na saúde e na conservação das tartarugas marinhas.

Palavras-chave:
Helmintos; Tartarugas marinhas; Índices parasitológicos; América do Sul

INTRODUCTION

Sea turtles have been considered one of the most endangered species of animals in the world (Valdivia et al., 2019VALDIVIA, A.; WOLF, S.; SUCKLING, K. Marine mammals and sea turtles listed under the US Endangered Species Act are recovering. PloS One, v.14, p.e0210164, 2019.). Of cosmopolitan distribution, these reptiles are belonging to the order Testudines and represented by only seven species, in which five inhabit the Brazilian coast (i.e., Caretta caretta, Chelonia mydas, Eretmochelys imbricata, Lepidochlelys olivacea and Dermochelys coriacea) (Mazaris et al., 2017MAZARIS, A.D.; SCHOFIELD, G.; GKAZINOU, C. et al. Global sea turtle conservation successes. Sci. Adv., v.3, p.e1600730, 2017.). The current perspective of conservation of these animals is worrying since several factors affect their survival (Tagliolatto et al., 2020TAGLIOLATTO, A.B.; GOLDBERG, D.W.; GODFREY, M.H. et al. Spatio‐temporal distribution of sea turtle strandings and factors contributing to their mortality in south‐eastern Brazil. Aquat. Conserv. Mar. Freshwater Ecosyst., v.30, p.331-350, 2020.), including anthropic actions (Farias et al., 2019FARIAS, D.S.D.; ALENCAR, A.E.B.; BOMFIM, A.C. et al. Marine turtles stranded in northeastern Brazil: composition, spatio-temporal, distribution and anthropogenic interactions. Chelonian Conserv. Biol., v.18, p.105-111, 2019.; Mashkour et al., 2020MASHKOUR, N.; JONES, K.; KOPHAMEL, S. et al. Disease risk analysis in sea turtles: A baseline study to inform conservation efforts. PloS One, v.15, p.e0230760, 2020.). The main impacts are related to negative interaction with fishing activity, solid waste ingestion, disorderly and growing occupation of the coastal strip and habitat degradation (Farias et al., 2019; Valdivia et al., 2019).

However, natural aspects such as predation, ecological changes and infectious diseases caused by viruses, bacteria and/or parasites may also contribute to decline of these populations (Mashkour et al., 2020MASHKOUR, N.; JONES, K.; KOPHAMEL, S. et al. Disease risk analysis in sea turtles: A baseline study to inform conservation efforts. PloS One, v.15, p.e0230760, 2020.). The parasite fauna of sea turtle is few studied, but includes helminths, protozoa, arthropods, and annelids. These parasites are well adapted to the marine environment and Chelonians are infected during long-distance migrations to reproduce or change seasonal habitats (Mashkour et al., 2020). Over the last years, parasitism by trematodes such as Neoctangium travassosi (Family Microscaphidiidae) has been reported in these animals (Werneck et al., 2015aWERNECK, M.R.; LIMA, E.H.S.M.; PIRES, T. et al. Helminth parasites of the juvenile hawksbill turtle Eretmochelys imbricata (Testudines: Cheloniidae) in Brazil. J. Parasitol., v.101, p.500-503, 2015a.; Meira Filho et al., 2017), being this species (N. travassosi) firstly identified in a turtle (unidentified species) on the south coast of the state of São Paulo, Brazil (Ruiz, 1943RUIZ, J.M. Neoctangium travassosi, gen. n., sp. n. (Trematoda: Paramphistomoidea), parasito de quelônio marinho. Chave da família Microscaphidiidae Travassos, 1922. Mem. Inst. Butantan, v.17, p.35-45, 1943.). The Family Microscaphidiidae with 22 described genera, represents a group of gastrointestinal trematodes that parasitize marine and freshwater turtles (Blair, 1987BLAIR, D. A revision of the subfamily Octangiinae (Platyhelminthes: Digenea: Microscaphidiidae) parasitic in marine turtles (Reptilia: Chelonia). Aust. J. Zool., v.35, p.75-92, 1987.).

Studies through standings in the northern coast of Rio Grande do Norte and east of Ceará (Bacia Potiguar) point this region as being of great importance for sea turtles, with records of the five species that occur in Brazil (Farias et al., 2019FARIAS, D.S.D.; ALENCAR, A.E.B.; BOMFIM, A.C. et al. Marine turtles stranded in northeastern Brazil: composition, spatio-temporal, distribution and anthropogenic interactions. Chelonian Conserv. Biol., v.18, p.105-111, 2019.). In fact, the real impact of this kind of parasitism on the health of sea turtles is difficult to assess. However, it is believed that these parasites present minor pathological relevance, especially because in some cases a high burden of parasites has been observed in healthy animals. The aim of this study was to report the occurrence of N. travassosi in sea turtles stranded in the Potiguar Basin, Northestern Brazil.

MATERIAL AND METHODS

Sea turtles stranded from 2010 to 2019, in an area known as Potiguar Basin, northeastern Brazil, were used in this study. The Beach Monitoring Program in the Potiguar Basin (Programa de Monitoramento de Praias da Bacia Potiguar - PMP-BP) has been conducted by Projeto Cetáceos da Costa Branca - Universidade do Estado do Rio Grande do Norte (PCCB-UERN), and it complies with the environmental constraint enforced by the Brazilian Institute of the Environment and Renewable Natural Resources (IBAMA) over the activities operated by PETROBRAS (Petróleo Brasileiro S.A., agreement number 2500.005657510.2). In addition, all procedures herein performed were authorized by the IBAMA (n. 13694-12).

All animals were morphologically identified, and measurements of carapace obtained. Curved carapace length (nuchal to notch length between supracaudal scales) was recorded using a flexible tape (Bolten, 1999BOLTEN, A.B. Techniques for measuring sea turtles. In: ECKERT, K.L.; BJORNDAL, K.L.; ABRU-GROBOIS, F.A.; DONNELLY, M. (Eds.). Research and management techniques for the conservation of sea turtles. Washington, USA: IUCN SSC Marine Turtle Specialist Group, 1999. p.110-114.).

At post-mortem examination all organs were examined, and the characteristics of lesions were recorded in clinical charts. They were carefully inspected, and parasites were manually collected. Specimens were measured, slides were prepared by the regression stain method, and finally observed under an optical microscope (40x and 100x). Photomicrographs were acquired using a digital camera (CMOS-5.0) mounted directly on the microscope (New Optics NO 226). The software TCapture 4.3 was used for the image acquisition and measurements of parasitic structures.

All specimens were morphologically identified using the taxonomic keys (Blair, 1987BLAIR, D. A revision of the subfamily Octangiinae (Platyhelminthes: Digenea: Microscaphidiidae) parasitic in marine turtles (Reptilia: Chelonia). Aust. J. Zool., v.35, p.75-92, 1987.; Gibson et al., 2002GIBSON, D.I.; JONES, A.; BRAY, R.A. Keys to the trematoda. Wallingford, UK: CABI Publishing and The Natural History Museum, 2002. 521p.). Then, ecological parasitic indexes such as prevalence (P), mean intensity (MI) and mean abundance (MA) were calculated (Bush et al., 1997BUSH, A.O.; LAFFERTY, K.D.; LOTZ, J.M. et al. Parasitology meets ecology on its own terms: Margolis et al. revisited. J. Parasitol., v.83, p.575-583, 1997.).

RESULTS

During the whole study period (from 2010 to 2019), a total of 80 Chelonia mydas and five Eretmochelys imbricata were studied. The species C. mydas presented a curvilinear carapace length (CCL) ranging from 28 to 118 cm (64.9±32.5cm), and curvilinear carapace width (CCW) varying from 26.2 to 110 cm (60.4±31.1). Conversely, the E. imbricata presented a curvilinear carapace length (CCL) and curvilinear carapace width (CCW) ranging from 87 to 89 cm (88±1cm), and from 75 to 85.5 cm (78.5±6cm), respectively.

The parasites herein retrieved were identified as belonging to the Family Microscaphidiidae (subclass Digenea) and species Neoctangium travassosi (Fig. 1).

Morphologically, they featured a lanceolate tick body. Tail-dorsal transverse edge notched in the midline and with muscle thickening at each extremity, also present in each postero-lateral margin. Terminal oral opening, with rounded to rectangular mouth cup in ventral view. The esophagus measured up to 18% of the body's length and the presence of a muscle bulb was observed at the posterior end. The caeca (intestine) were broad, wrinkled or dilated with the presence of food material, ending near the end of the body. Testicles indented, inter-caecal in the middle third of the body. Seminal vesicle beginnings in front of anterior testicle. Fibrous sac surrounding the terminal genitalia slightly developed. A ventral genital pore immediately behind the suction cup was observed. Small, ventral, sub-median ovary to the right side slightly behind the posterior testicles. The uterus was located between the Mehlis gland and the testicles. Lateral vitelline fields with anterior limit close to the point of contact between the testicles, posterior limit slightly before the ends of the head. Compact median field behind Mehlis's gland. Eggs in the uterus capped. Subterminal excretory pores, ventral to caudal crest.

Figure 1
Neoctangium travassosi adult collected in the gastrointestinal tract of Chelonia mydas. OS, oral sucker; ES, esophagus; PH, pharynx; T1 and T2, testicles; YF, yolk follicles; CA, caeca; LE, ledge; E, eggs; OV, ovaries; GM, glandule of Mehlis

Curiously, N. travassosi retrieved in C. mydas presented distinct measures from those parasites detected in E. imbricata (Table 1).

The ecological parasitic indexes for C. mydas were P = 20%, MI = 4.19 and MA = 0.84, whereas for E. imbricata they were P = 60%, MI = 1.67 and MA = 1.0. It is important to highlight that only juvenile sea turtles were parasitized by N. travassosi.

Table 1
Comparison of measurements of specimens of N. travassosi retrieved in the present study and those reported in the scientific literature

DISCUSSION

This study reported the occurrence of N. travassosi in sea turtles from South America and registered for the first time the presence of this parasite in E. imbricata in this region. The measurements of CCL and CCW for C. mydas and for E. imbricata were like those previously reported (Werneck et al., 2015aWERNECK, M.R.; LIMA, E.H.S.M.; PIRES, T. et al. Helminth parasites of the juvenile hawksbill turtle Eretmochelys imbricata (Testudines: Cheloniidae) in Brazil. J. Parasitol., v.101, p.500-503, 2015a., 2015b). The detection of N. travassosi parasitizing these turtle species is very important, especially because it is believed that this genus has this single species that was firstly identified in Brazil in 1943 in a sea turtle (Blair, 1987BLAIR, D. A revision of the subfamily Octangiinae (Platyhelminthes: Digenea: Microscaphidiidae) parasitic in marine turtles (Reptilia: Chelonia). Aust. J. Zool., v.35, p.75-92, 1987.). Interestingly, the morphometric features presented by the parasites infecting C. mydas were slightly distinct from those detected in E. imbricata (see Tab. 1). Most likely, this difference may be related to the stage of maturity presented by each parasite, or by a better adaptation of these trematodes to the species C. mydas, the sea turtle in which they were more developed. Nonetheless, it is important to note that the anatomical features of specimens herein reported corroborates with characteristics previously reported in a study in Panama (Blair, 1987).

The prevalence observed in this research (20% for C. mydas and 60% for E. imbricata) is similar to those detected in other studies (Binoti et al., 2016BINOTI, E.; GOMES, M.C.; CALAIS JR, A. et al. Helminth fauna of Chelonia mydas (Linnaeus, 1758) in the south of the State of Espírito Santo and description of tissue injury. Helminthologia, v.53, p.195-199, 2016.). However, the low values of MI and MA herein obtained indicate that most likely animals that occur in Northeastern coast of Brazil are less susceptible to the infection by this parasite species. Only juvenile turtles were parasitized. This pattern of infection has already been observed in the Brazilian coast. For instance, the helminths fauna of animals on the coast of the states of the Southeast Brazil were detected predominantly in young animals (Werneck et al., 2015aWERNECK, M.R.; LIMA, E.H.S.M.; PIRES, T. et al. Helminth parasites of the juvenile hawksbill turtle Eretmochelys imbricata (Testudines: Cheloniidae) in Brazil. J. Parasitol., v.101, p.500-503, 2015a.). Similarly, this same pattern has been observed in E. imbricata in the states of Ceará, Bahia, São Paulo, and Espírito Santo (Werneck et al., 2015a, 2015b).

It is believed that the feeding behavior dictates the nature of helminth communities, including N. travassosi, in sea turtle species (Werneck et al., 2015aWERNECK, M.R.; LIMA, E.H.S.M.; PIRES, T. et al. Helminth parasites of the juvenile hawksbill turtle Eretmochelys imbricata (Testudines: Cheloniidae) in Brazil. J. Parasitol., v.101, p.500-503, 2015a.). At the beginning of life, C. mydas are primarily omnivorous and, when adults tend towards an herbivorous diet. On the other hand, young E. imbricata feed predominantly on invertebrates (mollusks) and sea sponges (Werneck et al., 2015a). Considering mollusks have intermediate host of some digenetic parasites, these animals are highly exposed to the risk of infection in its natural habitats. In addition, these Chelonians frequented the same feeding grounds, where they possibly acquired the infective form of these trematodes (Binoti et al., 2016BINOTI, E.; GOMES, M.C.; CALAIS JR, A. et al. Helminth fauna of Chelonia mydas (Linnaeus, 1758) in the south of the State of Espírito Santo and description of tissue injury. Helminthologia, v.53, p.195-199, 2016.). It is worth mentioning that C. mydas is faithful to its foraging site close to the coast, that is, the species maintains a continuous and long-term residence in a certain location (Mashkour et al., 2020MASHKOUR, N.; JONES, K.; KOPHAMEL, S. et al. Disease risk analysis in sea turtles: A baseline study to inform conservation efforts. PloS One, v.15, p.e0230760, 2020.), which may contribute to the maintenance of the cycle of life of parasites carried by this species.

Ruiz first identified the trematode species N. travassosi in 1943RUIZ, J.M. Neoctangium travassosi, gen. n., sp. n. (Trematoda: Paramphistomoidea), parasito de quelônio marinho. Chave da família Microscaphidiidae Travassos, 1922. Mem. Inst. Butantan, v.17, p.35-45, 1943.. A few years later the genus was renamed as Octangium based in some morphological features such as the presence of paired caudal papillae (Yamaguti, 1971YAMAGUTI, S. Synopsis of digenetic trematodes of vertebrate. Tokyo: Keigaku Publishing, 1971. 1074p.). Subsequently, after a careful morphological examination (elongated and curved bladder, absence of rosette of diverticula and presence of ventral excretory pore) of some specimens two genera were validated (Neoctangium and Octangium) (Blair, 1987BLAIR, D. A revision of the subfamily Octangiinae (Platyhelminthes: Digenea: Microscaphidiidae) parasitic in marine turtles (Reptilia: Chelonia). Aust. J. Zool., v.35, p.75-92, 1987.). Since there, other reports of N. travassosi parasitizing C. mydas were made in Brazil (Binoti et al., 2016BINOTI, E.; GOMES, M.C.; CALAIS JR, A. et al. Helminth fauna of Chelonia mydas (Linnaeus, 1758) in the south of the State of Espírito Santo and description of tissue injury. Helminthologia, v.53, p.195-199, 2016.), Caribe (Gupta and Mehrotra, 1981GUPTA, S.P.; MEHROTRA, V. On two blood flukes (Trematoda) of the family Spirorchidae Stunkard, 1921 from Indian marine turtles. Acta Parasitol. Pol., v.28, p.11-20, 1981.) and Trinidad (Gupta, 1961), as well as in E. imbricata on the coast of Porto Rico (Fischthal and Acholonu, 1976FISCHTHAL, J.H.; ACHOLONU, A.D. Some digenetic trematodes from atlantic hawksbill turtle Eretmochelys imbricata imbricate (L.) from Puerto Rico. J. Helminthol. Soc., v.43, p.174-185, 1976.) and Panama (Blair, 1987).

The determination of pathogenic role of these parasites in the health of turtles is difficult to assess, especially considering that were wild stranded animals without any previous information. Undoubtedly, anthropic interactions have been considered important threats for sea turtles, being responsible for about 60% of causa mortis, whereas it is estimated that parasitic infections may be related in about 13% of deaths of these animals (Morais, 2018MORAIS, I.C.C. Fatores de óbito em tartarugas marinhas da bacia potiguar RN/CE. 2018. 61f. Dissertação (Mestrado em Programa de Pós Graduação em Ciências Naturais), Universidade do Estado do Rio Grande do Norte, Mossoró, RN.).

CONCLUSION

This study revealed the parasitism by N. travassosi in C. mydas and E. imbricata in the Brazilian coast. It is important to note that this is the first report of the infection by this parasite in E. imbricata in the South America, enlarging the occurrence area of this parasite as well as the plethora of hosts. Finally, the retrieval of these parasites represents a warning for the need of further studies to assess the role of this kind of parasitism on the health of animals, and the impact on the conservation of sea turtles.

ACKNOWLEDGEMENTS

R.A.N.R received a research fellowship from CNPq (Bolsa de Produtividade; grant no. 305971/2021-2).

REFERENCES

  • BINOTI, E.; GOMES, M.C.; CALAIS JR, A. et al. Helminth fauna of Chelonia mydas (Linnaeus, 1758) in the south of the State of Espírito Santo and description of tissue injury. Helminthologia, v.53, p.195-199, 2016.
  • BLAIR, D. A revision of the subfamily Octangiinae (Platyhelminthes: Digenea: Microscaphidiidae) parasitic in marine turtles (Reptilia: Chelonia). Aust. J. Zool., v.35, p.75-92, 1987.
  • BOLTEN, A.B. Techniques for measuring sea turtles. In: ECKERT, K.L.; BJORNDAL, K.L.; ABRU-GROBOIS, F.A.; DONNELLY, M. (Eds.). Research and management techniques for the conservation of sea turtles. Washington, USA: IUCN SSC Marine Turtle Specialist Group, 1999. p.110-114.
  • BUSH, A.O.; LAFFERTY, K.D.; LOTZ, J.M. et al. Parasitology meets ecology on its own terms: Margolis et al. revisited. J. Parasitol., v.83, p.575-583, 1997.
  • FARIAS, D.S.D.; ALENCAR, A.E.B.; BOMFIM, A.C. et al. Marine turtles stranded in northeastern Brazil: composition, spatio-temporal, distribution and anthropogenic interactions. Chelonian Conserv. Biol., v.18, p.105-111, 2019.
  • FISCHTHAL, J.H.; ACHOLONU, A.D. Some digenetic trematodes from atlantic hawksbill turtle Eretmochelys imbricata imbricate (L.) from Puerto Rico. J. Helminthol. Soc., v.43, p.174-185, 1976.
  • GIBSON, D.I.; JONES, A.; BRAY, R.A. Keys to the trematoda. Wallingford, UK: CABI Publishing and The Natural History Museum, 2002. 521p.
  • GUPTA, S.P. On some trematodes from the intestine of the marine turtle, Chelone mydas, from the Caribbean Sea. Can. J. Zool., v.39, p.293-298, 1961.
  • GUPTA, S.P.; MEHROTRA, V. On two blood flukes (Trematoda) of the family Spirorchidae Stunkard, 1921 from Indian marine turtles. Acta Parasitol. Pol., v.28, p.11-20, 1981.
  • MASHKOUR, N.; JONES, K.; KOPHAMEL, S. et al. Disease risk analysis in sea turtles: A baseline study to inform conservation efforts. PloS One, v.15, p.e0230760, 2020.
  • MAZARIS, A.D.; SCHOFIELD, G.; GKAZINOU, C. et al. Global sea turtle conservation successes. Sci. Adv., v.3, p.e1600730, 2017.
  • MEIRA FILHO, M.R.C.; ANDRADE, M.F.; DOMIT, C. et al. A review of helminths of the green turtle (Chelonia mydas) in Brazil. Oecol. Aust., v.21, p.17-26, 2017.
  • MORAIS, I.C.C. Fatores de óbito em tartarugas marinhas da bacia potiguar RN/CE. 2018. 61f. Dissertação (Mestrado em Programa de Pós Graduação em Ciências Naturais), Universidade do Estado do Rio Grande do Norte, Mossoró, RN.
  • RUIZ, J.M. Neoctangium travassosi, gen. n., sp. n. (Trematoda: Paramphistomoidea), parasito de quelônio marinho. Chave da família Microscaphidiidae Travassos, 1922. Mem. Inst. Butantan, v.17, p.35-45, 1943.
  • TAGLIOLATTO, A.B.; GOLDBERG, D.W.; GODFREY, M.H. et al. Spatio‐temporal distribution of sea turtle strandings and factors contributing to their mortality in south‐eastern Brazil. Aquat. Conserv. Mar. Freshwater Ecosyst., v.30, p.331-350, 2020.
  • VALDIVIA, A.; WOLF, S.; SUCKLING, K. Marine mammals and sea turtles listed under the US Endangered Species Act are recovering. PloS One, v.14, p.e0210164, 2019.
  • WERNECK, M.R.; AMORIN, D.B.; BLAIR, D. Olive ridley sea turtle Lepidochelys olivacea (Eschscholtz, 1829) from Brazil as a new host of Pyelosomum cochlear Looss, 1899 (Digenea: Pronocephalidae). Comp. Parasitol., v.82, p.144-147, 2015b.
  • WERNECK, M.R.; LIMA, E.H.S.M.; PIRES, T. et al. Helminth parasites of the juvenile hawksbill turtle Eretmochelys imbricata (Testudines: Cheloniidae) in Brazil. J. Parasitol., v.101, p.500-503, 2015a.
  • YAMAGUTI, S. Synopsis of digenetic trematodes of vertebrate. Tokyo: Keigaku Publishing, 1971. 1074p.

Publication Dates

  • Publication in this collection
    17 Apr 2023
  • Date of issue
    Mar-Apr 2023

History

  • Received
    13 July 2022
  • Accepted
    07 Nov 2022
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