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P e n t a s t o m i a s i s i n A u s t r a l i a n c r o c o d i l i a n s Fact sheet Introductory statement Pentastomiasis (also known as Porocephalosis) is a disease caused by infection with pentastomids. Pentastomids are endoparasites of the respiratory system of vertebrates, maturing primarily in the respiratory system of carnivorous reptiles (90% of all pentastomid species), but also in toads, birds and mammals. Pentastomids have zoonotic potential although no human cases have been reported in Australia. These parasites have an indirect life cycle involving one or more intermediate host. They may be distinguished from other parasite taxa by the presence of four hooks surrounding their mouth, which they use for attaching to respiratory tissue to feed on host blood. Pentastomid infections may be asymptomatic, but adult and larval pentastomids can cause severe pathology resulting in the death of their intermediate and definitive hosts, usually via obstruction of airways or secondary bacterial and/or fungal infections. Both species of Australian crocodilians are host to pentastomids and these infections have been linked to crocodile morbidity and mortality. Aetiology Pentastomiasis in crocodilians is caused by endoparasitic metazoans of the subclass Pentastomida. Four genera of pentastomids are known to infect crocodilians in Australia: Alofia, Leiperia, Sebekia, and Selfia; these genera are all in the Family Sebekidae (Order: Porocephalida). Natural hosts Definitive hosts There are two species of crocodilians in Australia, the freshwater crocodile (Crocodylus johnstoni) and the estuarine or saltwater crocodile (Crocodylus porosus); both host pentastomids (see Table 1). Within Australia Crocodylus porosus hosts six species of pentastomid and C. johnstoni hosts three species. Pentastomids have been recovered from the nasal passages, trachea, bronchus, bronchi, bronchioles, lungs and the major blood vessels (aorta and pulmonary artery) of the heart. Body sizes of these pentastomids range from relatively small (11 mm in Sebekia multiannulata) to quite large (75 mm in Leiperia australiensis).

Table 1. Known pentastomid species that infect crocodilians within Australia. Host species Pentastome species Reference Freshwater crocodile Leiperia australiensis (Riley and Huchzermeyer 1996) (Crocodylus johnstoni) Sebekia johnstoni (Riley et al. 1990) Sebekia multiannulata (Riley et al. 1990) Estuarine crocodile Alofia merki (Riley 1994) (Crocodylus porosus) Leiperia australiensis (Riley and Huchzermeyer 1996) Sebekia johnstoni (Riley et al. 1990) Sebekia multiannulata (Riley et al. 1990) Sebekia purdieae (Riley et al. 1990) Selfia porosus (Riley 1994) Intermediate hosts: Though field data are lacking, fish are intermediate hosts for all pentastomids that infect Australian crocodiles. In the Americas, Sebekia spp. may utilise snakes, lizards, turtles and mammals as additional intermediate hosts (Boyce 1985; Overstreet et al. 1985; Winch and Riley 1986); it is unknown whether the same is true for Australia. World distribution Australasia, Africa, and the Americas. Fourteen of the 23 extant species of crocodilians are known to host pentastomids. Of the six genera that infect crocodilians, four occur in Australia: Alofia spp. occur in Africa, Samoa, the Philippines, India and Australia; Leiperia spp. occur in Africa, the Americas and Australia; Sebekia spp. occur in Africa, the Americas, Trinidad, South East Asia, Papua New Guinea, and Australia; Selfia is a monotypic genus containing only the species Selfia porosus that exclusively infects C. porosus in Australia (Junker and Boomker 2006). Data on pentastomiasis prevalence in wild crocodilians is primarily restricted to Sebekia mississippiensis in American alligators (Alligator mississippiensis) in southeastern USA; infections are common, occurring in 81-96% of alligators (Cherry and Ager 1982; Boyce 1985; Tellez et al. 2016). Occurrences in Australia Within Australia, the disease has only been formally documented in Queensland and the Northern Territory (Riley et al. 1990; Buenviaje et al. 1994; Riley 1994; Riley and Huchzermeyer 1996), however it is likely to occur in all other states that crocodilians occur (i.e. Western Australia). Data on pentastomiasis in wild Australian crocodiles is lacking; in captivity, pentastomids infected 90% of 10 crocodiles at a crocodile farm at Innisfail, Queensland (Buenviaje et al. 1994). Epidemiology Basic life cycle Adult female pentastomids continuously lay eggs in the lungs, amounting to millions of eggs per female. Eggs leave the lungs with host fluid and pass into the mouth or are swallowed into the digestive tract. WHA Fact sheet: Pentastomiasis in Australian crocodilians April 2016 2

Eggs pass out into the environment when the crocodile expels fluid orally, or defecates Eggs remain viable for months. Eggs are consumed by a suitable fish intermediate host. Within the fish, primary larvae migrate to viscera, muscles, or the swim bladder, encyst and develop into infective larvae. Infective larvae enter the crocodile when it consumes an infected fish. Infective larvae burrow out of the crocodile s gastrointestinal tract and enter the major vessels of the heart (aorta and pulmonary artery), in Leiperia spp., or the respiratory tract (nasal passages, trachea, bronchus, bronchi, bronchioles and lungs), in all other genera Developing pentastomids feed on host blood and develop into mature adults. Adult Leiperia pentastomids migrate out of the blood vessels and into the respiratory tract (trachea, bronchus, bronchi, bronchioles and lungs). Male and female pentastomes mate once (presumably in the respiratory tract, not within the blood vessels), females store sperm and begin laying eggs to complete the life cycle. Sources of infectious agent The oral and nasal secretions (i.e. saliva and mucous) and faeces of an infected crocodile contain pentastomid eggs. These eggs will not develop to the blood-feeding adult stage without passing through an intermediate host. Morbidity and mortality The morbidity and mortality rate is unknown for this disease in Australia. However, in captive C. porosus and New Guinea crocodiles (Crocodylus novaeguineae) 15% (eight) of 54 ill or deceased crocodiles were afflicted by pentastomiasis (Sebekia sp.; Ladds and Sims 1990). Other crocodilian species have died from pentastomid infections, e.g. four of four captive African dwarf crocodile (Osteolaemus tetraspis) hatchlings died after becoming infected with Sebekia mississippiensis, presumably contracted via consumption of infected fish (mean = 7 pentastomids per crocodile; Adams et al. 2001). Young crocodiles are considered particularly susceptible to disease caused by pentastomids (Boyce et al. 1984), though dietary differences between hatchling and adult crocodiles (whereby hatchlings rarely eat fish) may preclude pentastomid infections in wild hatchlings (Moreland et al. 1989). Morbidity may be caused by larvae migrating from the gastrointestinal tract to infection sites, causing scarring and interfering with organ function (Riley 1986). Crocodile pentastomids spend a significant portion of their lives inside the large vessels of the heart, conceivably, these infections could cause vascular blockage. The mouthparts and hooks of adult pentastomids may pierce respiratory tissue, leading to pulmonary haemorrhage and/or bacterial infections that may culminate in chronic pneumonia (Jacobson 2007; Paré 2008). Since pentastomids feed on host blood, it is plausible that heavy infections may cause anaemia, though there are no published accounts of this. In addition, Australian crocodilians can possess multiple species of pentastomids concurrently which may enhance their pathology (Riley et al. 1990). Heavily infected fish intermediate hosts can die from their infections whilst others show no morbidity. Clinical signs Commonly, there are no clinical signs of infection with pentastomids. Crocodiles adversely affected by pentastomiasis will likely present with nonspecific symptoms of disease (such as anorexia, lethargy or sudden WHA Fact sheet: Pentastomiasis in Australian crocodilians April 2016 3

death) or more specific symptoms of respiratory disease. Clinical signs of respiratory disease include nasal discharge, laboured or rapid breathing, abnormal swimming, excessive basking and anorexia. In weak animals, the basihyal valve can malfunction, allowing food or water to enter the airways; aspiration does not occur in healthy crocodiles. There are multiple other causative agents for respiratory disease (e.g. bacterial and fungal infections) that should be considered alongside pentastomiasis (see Differential diagnoses below). Diagnosis Tracheal wash, cloacal wash and faecal flotation to detect pentastomid eggs. Radiograph to detect adult pentastomids in the respiratory tract. Endoscopic or surgical examination of the respiratory tract. Presence of live pentastomids exiting the crocodile (pentastomids often crawl out of stressed or dying hosts). Direct examination of the respiratory tract and major blood vessels of the heart during necroscopy. Clinical pathology There are no consistent clinical signs of pentastomiasis in crocodilians. Pathology Piercing of the respiratory tissue by the pentastomid hooks and mouthparts can facilitate secondary bacterial and fungal infections. Large pentastomids such as Leiperia spp. may cause substantial lesions at feeding sites and puncture the lung. Pentastomiasis may cause pulmonary oedema and haemorrhage, and when infections are comprised of large and/or numerous pentastomids they can physically occlude respiratory passages leading to suffocation (Jacobson 2007). The pathological effects of Leiperia inhabiting the major blood vessels of the heart are yet to be evaluated though obstruction of blood flow and blockage of vessels are likely consequences. Macroscopically, in Australian crocodilians, adult pentastomids are visible in respiratory tissue and infected lungs have red to black consolidated foci (up to 15 mm) visible beneath the pleura. Microscopically, these dark foci are composed of pentastomids and their eggs, haemorrhage, and mononuclear and giant cell accumulation (often surrounding the pentastomid eggs). Some cases have associated severe disseminated focal exudative pneumonia. One case presented occlusion and distension of the bronchioles in association with heavy pentastomid presence. Further pathology includes extensive interstitial pneumonia, emphysema, bronchiectasis, granulomas and hyperplasia of the bronchiolar epithelium (Ladds and Sims 1990; Buenviaje et al. 1994; Ladds et al. 1995; Ladds 2009). In Nile crocodiles (Crocodylus niloticus), infections with the same genera of pentastomids that infect Australian crocodilians caused mild coagulative necrosis with heterophilic and eosinophilic infiltrates and adjacent haemorrhage and oedema at the sites where pentastomids were attached (Junker et al. 1999). In one case, the endothelial lining of the aorta had ulceration and inflammation associated with an attached pentastomid (Junker et al. 1999). One ill and emaciated crocodile exhibited obstruction of the bronchi and pulmonary aorta by Leiperia cincinnalis. The migration of blood-feeding immature pentastomids across the outside surface of the trachea was evident as a serious of brown nodules. Lesions caused by pentastomids WHA Fact sheet: Pentastomiasis in Australian crocodilians April 2016 4

exhibited abundant fungal hyphae and necrotic bacterial colonies, likely as secondary infections (Junker et al. 1999). In American alligators, fatal infections were caused by a genus (Sebekia) that infects Australian crocodilians. In adults, pulmonary necrosis and haemorrhage was apparent, blood filled the lungs, stomach, and in some cases, the intestines, culminating in death (Deakins 1971). Other cases revealed nymphs in the liver in association with necrosis and haemorrhage (Hazen et al. 1978). In hatchlings, symptoms of anorexia and respiratory distress culminated in death; pathological signs included pulmonary haemorrhage, collapsed air sacs and hepatic lipidosis (Boyce et al. 1984). Differential diagnoses Since there are no definitive clinical symptoms of pentastomiasis the disease must be diagnosed via direct observation of pentastomid eggs or adults; both life history stages are distinctive and may not be confused with any other disease agent. Symptoms of respiratory disease in crocodiles can often be confused with those of neurologic disease. For example, West Nile virus infection produces clinical signs consistent with respiratory disease in American alligators (Nevarez 2006). In crocodilians, respiratory disease is most commonly caused by bacterial or fungal infections, either cause should be considered when making a diagnosis. Laboratory diagnostic specimens & procedures Fresh samples are preferred since the diagnostic features of pentastomid eggs become obscured with dehydration caused by chemical preservation. However, for practicality, fluid (from tracheal and cloacal washes) and faecal samples (1 ml) preserved in 70% ethanol may suffice. Microscopic examination (using the 40X objective on a compound microscope) of these samples will allow detection of pentastomid eggs (Kelehear et al. 2013). Treatment Treatment is not generally recommended except in captive (e.g. farmed or zoo animals) or endangered animals that are showing adverse clinical signs of infection and have been diagnosed with pentastomiasis. Surgical or endoscopic removal is the most reliable method for eliminating infections (Greiner and Mader 2006; Brock et al. 2012). There is no reliable chemotherapeutic treatment but anecdotal reports suggest that Ivermectin may be successful (Paré 2008). However, treatment with drugs is complicated by the large size and number of pentastomids comprising crocodilian infections, and the fact that these parasites can dwell in the major vessels of the heart. Killing the parasites with drugs and leaving these dead parasites in situ could induce secondary bacterial infections or cardiovascular distress as the crocodile s immune system attempts to dispose of them (Jacobson 2007). Prevention and control Pentastome eggs are very resilient and able to survive at least two weeks of desiccation and six months of refrigeration (Self 2009). WHA Fact sheet: Pentastomiasis in Australian crocodilians April 2016 5

Pentastomiasis can be prevented in captivity by feeding crocodiles captive-bred food (since wild caught food may be infected with intermediate stages of the pentastome life cycle). Alternatively, food should be frozen at -10 C for at least 72 hours to kill pentastome larvae; freezing fish for less than 72 hours prior to feeding can cause pentastomid infections (Buenviaje et al. 1994). Since the life cycle is indirect, infections should be self-limiting over time in captivity if crocodiles are not housed with live fish. Note however that pentastomids are quite long-lived (e.g. up to 8 years in some species; Storch 1993). To prevent establishment of the life cycle, and re-infections, crocodiles (definitive hosts) should not be housed with live fish (intermediate hosts). Thorough washing and disinfecting of surfaces that have been in contact with crocodiles and their secretions and excrement is recommended to prevent transfer of infections. Humans: Basic hygiene such as wearing gloves and washing hands thoroughly with hot soapy water after being in contact with crocodiles and crocodile products should preclude ingestion of pentastomid eggs or larvae. Note that pentastomids do not develop past the larval stage in humans. Surveillance and management There is no targeted surveillance or management of this disease in Australia. Wildlife disease surveillance in Australia is coordinated by the Wildlife Health Australia. The National Wildlife Health Information System (ewhis) captures information from a variety of sources including Australian government agencies, zoo and wildlife parks, wildlife carers, universities and members of the public. Coordinators in each of Australia's States and Territories report monthly on significant wildlife cases identified in their jurisdictions. NOTE: access to information contained within the National Wildlife Health Information System dataset is by application. Please contact admin@wildlifehealthaustralia.com.au. Research Key areas for future research Taxonomy: one or more undescribed species of pentastomid may infect Australian estuarine crocodiles; this was first proposed by Riley et al. (1985) but there has been no further research on the matter Life cycle: intermediate host taxa what species of fish are involved? do other taxa (besides fish) act as viable intermediate hosts? Life cycle: duration of each stage of the life cycle how long are fish infective? how long do the parasites live in the blood vessels and the respiratory tract? Prevalence of infections does infection prevalence differ with crocodile age? are young freshwater crocodiles pentastomid free since they eat mainly insects? Severity of the disease what is the impact of pentastomiasis on wild crocodiles? what is the impact of pentastomiasis on commercial crocodile enterprises? Geographic distribution of pentastomids in crocodilians do they occur in WA, or only the NT and Qld, as current knowledge implies? WHA Fact sheet: Pentastomiasis in Australian crocodilians April 2016 6

Human health implications Pentastomids are zoonotic parasites though most human cases of pentastomiasis are asymptomatic and present as an incidental finding at autopsy. 99% of human cases are caused by pentastomids of the genera Armillifer (from snakes) and Linguatula (from mammals) and are concentrated in the tropics and subtropics of Africa, Southeast Asia and the Middle East; neither genera infect crocodiles (Drabick 1987). There is a single case of a human being parasitised by pentastomids of crocodilians: the nymphs of Leiperia cincinnalis infected a human in Zaire (Fain 1975). However, the infection is expected to be the result of consumption of undercooked fish (intermediate host) harbouring infective larvae, rather than consumption of crocodile meat (Fain 1975). As a precautionary measure, it is recommended that raw crocodile meat (and fish) be handled in a sanitary manner and thoroughly cooked prior to consumption. There has never been a human case of pentastomiasis in Australia. Conclusions Little is known about pentastomiasis in wild crocodilians in Australia. For instance, for most species of pentastomid almost nothing is known of their life cycle (in particular, intermediate hosts), the extent of geographical distribution, or the effect on the host. Some captive crocodile deaths have been linked to pentastomid infections; research is required in this area to establish the influence of pentastomiasis on wild crocodilian health. References and other information Adams, L, Isaza, R, Greiner, E (2001) Fatal pentastomiasis in captive African dwarf crocodile hatchlings (Osteolaemus tetraspis). Journal of Zoo and Wildlife Medicine 32, 500-502. Boyce, W, Cardeilhac, P, Lane, T, Buergelt, C, King, M (1984) Sebekiosis in captive alligator hatchlings. Journal of the American Veterinary Medical Association 185, 1419-1420. Boyce, WM (1985) The prevalence of Sebekia mississippiensis (Pentastomida) in American alligators (Alligator mississippiensis) in north Florida and experimental infection of paratenic hosts. Proceedings of the Helminthological Society of Washington 52, 278-282. Brock, AP, Gallagher, AE, Walden, HDS, Owen, JL, Dunbar, MD, Wamsley, HL, Schoeller, AB, Childress, AL, Wellehan, JFXJ (2012) Kiricephalus coarctatus in an Eastern Indigo Snake (Drymarchon couperi); endoscopic removal, identification, and phylogeny Veterinary Quarterly 32, 107-112. Buenviaje, GN, Ladds, PW, Melville, L, Manolis, SC (1994) Disease-husbandry associations in farmed crocodiles in Queensland and the Northern Territory. Australian Veterinary Journal 71, 165-173. Cherry, RH, Ager, AL, Jr. (1982) Parasites of American alligators (Alligator mississippiensis) in South Florida. Journal of Parasitology 68, 509-510. Deakins, DE (1971) Pentastomes from Blackbeard Island, Georgia, with notes on North American pentastomes. Journal of Parasitology 57, 1197. Drabick, JJ (1987) Pentastomiasis. Reviews of Infectious Diseases 9, 1087-1094. Fain, A (1975) The pentastomida parasitic in man. Annales de la Société Belge de Médecine Tropicale 55, 59-64. WHA Fact sheet: Pentastomiasis in Australian crocodilians April 2016 7

Greiner, EC, Mader, DR (2006) Parasitology. In 'Reptile Medicine and Surgery.' (Ed. DR Mader.) pp. 343-364. (Saunders Elsevier: St. Louis). Hazen, TC, Aho, JM, Murphy, TM, Esch, GW, Schmidt, GD (1978) The parasite fauna of the American alligator (Alligator mississippiensis) in South Carolina. Journal of Wildlife Diseases 14, 435-439. Jacobson, ER (2007) Parasites and parasitic diseases of reptiles. In 'Infectious diseases and pathology of reptiles.' (Ed. ER Jacobson.) pp. 590-592. (Taylor & Francis Group: Boca Raton). Junker, K, Boomker, J (2006) A check-list of the pentastomid parasites of crocodilians and freshwater chelonians. Onderstepoort Journal of Veterinary Research 73, 27-36. Junker, K, Boomker, J, Bolton, LA (1999) Pentastomid infections in Nile crocodiles (Crocodylus niloticus) in the Kruger National Park, South Africa, with a description of the males of Alofia simpsoni. Onderstepoort Journal of Veterinary Research 66, 65-71. Kelehear, C, Brown, GP, Shine, R (2013) Invasive parasites in multiple invasive hosts: the arrival of a new host revives a stalled prior parasite invasion. Oikos 122, 1317-1324. Ladds, P (2009) Helminth, annelid and pentastome diseases in reptiles. In 'Pathology of Australian Native Wildlife.' (Ed. P Ladds.) pp. 345-366. (CSIRO publishing: Collingwood). Ladds, PW, Mangunwirjo, H, Sebayang, D, Daniels, PW (1995) Diseases in young farmed crocodiles in Irian Jaya. Veterinary Record 136, 121-124. Ladds, PW, Sims, LD (1990) Diseases of young captive crocodiles in Papua New Guinea. Australian Veterinary Journal 67, 323-330. Moreland, AF, Forrester, DJ, Delany, MF (1989) Sebekia mississippiensis (Pentastomida) from juvenile American alligators in north central Florida. Proceedings of the Helminthological Society of Washington 56, 42-43. Nevarez, J (2006) Crocodilian differential diagnosis. In 'Reptile Medicine and Surgery.' (Ed. DR Mader.) Vol. 2e pp. 705-714. (Saunders Elsevier: St. Louis). Overstreet, RM, Self, JM, Vliet, KA (1985) The pentastomid Sebekia mississippiensis sp. n. in the American alligator and other hosts. Proceedings of the Helminthological Society of Washington 52, 266-277. Paré, JA (2008) An overview of pentastomiasis in reptiles and other vertebrates. Journal of Exotic Pet Medicine 17, 285-294. Riley, J (1986) The biology of pentastomids. Advances in Parasitology 25, 45-128. Riley, J (1994) A revision of the genus Alofia Giglioli, 1922 and a description of a new monotypic genus, Selfia: two genera of pentastomid parasites (Porocephalida: Sebekidae) inhabiting the bronchioles of the marine crocodile Crocodylus porosus and other crocodilians. Systematic Parasitology 29, 23-41. Riley, J, Huchzermeyer, FW (1996) A reassessment of the pentastomid genus Leiperia Sambon, 1922 with a description of a new species from both the Indopacific crocodile Crocodylus porosus and Johnston's crocodile C. johnstoni in Australia. Systematic Parasitology 34, 53-66. Riley, J, Spratt, DM, Presidente, PJA (1985) Pentastomids (Arthropoda) parasitic in Australian reptiles and mammals. Australian Journal of Zoology 33, 39-53. WHA Fact sheet: Pentastomiasis in Australian crocodilians April 2016 8

Riley, J, Spratt, DM, Winch, JM (1990) A revision of the genus Sebekia Sambon, 1922 (Pentastomida) from crocodilians with descriptions of five new species. Systematic Parasitology 16, 1-25. Self, JT (2009) Pentastomida: tongue worms. In 'Gerald D. Schmidt & Larry S. Roberts' foundations of parasitology. 8th Edition.' (Eds LS Roberts, J Janovy.) pp. 561-568. (McGraw-Hill: New York). Storch, V (1993) Pentastomida. In 'Microscopic anatomy of invertebrates. Vol. 12. Onychophora, Chilopoda, and lesser Protostomata.' (Eds FW Harrison, ME Rice.) pp. 115-142. (Wiley-Liss: New York). Tellez, M, Haghighi, A, Lavihim, M (2016) Distribution and abundance of Sebekia mississippiensis (Sebekidae) in the American alligator, Alligator mississippiensis. Comparative Parasitology 81, 232-239. Winch, JM, Riley, J (1986) The development of Sebekia oxycephala (Pentastomida) from a South American crocodilian (Caiman sclerops sclerops) in experimentally infected fish. Zeitschrift für Parasitenkunde 72, 251-264. Acknowledgements We are extremely grateful to the people who had input into this fact sheet and would specifically like to thank Crystal Kelehear. Updated: 26 April 2016 To provide feedback on this fact sheet We are interested in hearing from anyone with information on this condition in Australia, including laboratory reports, historical datasets or survey results that could be added to the National Wildlife Health Information System. If you can help, please contact us at admin@wildlifehealthaustralia.com.au. Wildlife Health Australia would be very grateful for any feedback on this fact sheet. Please provide detailed comments or suggestions to admin@wildlifehealthaustralia.com.au. We would also like to hear from you if you have a particular area of expertise and would like to produce a fact sheet (or sheets) for the network (or update current sheets). A small amount of funding is available to facilitate this. Disclaimer This fact sheet is managed by Wildlife Health Australia for information purposes only. Information contained in it is drawn from a variety of sources external to Wildlife Health Australia. Although reasonable care was taken in its preparation, Wildlife Health Australia does not guarantee or warrant the accuracy, reliability, completeness, or currency of the information or its usefulness in achieving any purpose. It should not be relied on in place of professional veterinary consultation. To the fullest extent permitted by law, Wildlife Health Australia will not be liable for any loss, damage, cost or expense incurred in or arising by reason of any person relying on information in this fact sheet. Persons should accordingly make and rely on their own assessments and enquiries to verify the accuracy of the information provided. WHA Fact sheet: Pentastomiasis in Australian crocodilians April 2016 9