INTRODUCTION
Trypanosomes and Leishmania spp. are vector-borne parasites associated with severe disease in both animal and human hosts. The global distribution of Trypanosoma spp. and Leishmania spp. is heavily reliant on the presence of both reservoir hosts and competent vectors. Worldwide, cats (Felis catus) are reported to become infected by at least six Trypanosoma spp.; T. brucei, T. congolense, T. gambiense, T. cruzi, T. evansi and T. rangeli (Bowman et al. Reference Bowman, Hendrix, Lindsay and Barr2002). Likewise, 44 Trypanosoma spp. have been shown to infect rodents (Hoare, Reference Hoare1972; Milocco et al. Reference Milocco, Kamyingkird, Desquesnes, Jittapalapong, Herbreteau, Chaval, Douangboupha and Morand2013; Pumhom et al. Reference Pumhom, Morand, Tran, Jittapalapong and Desquesnes2015). Leishmania spp. are also zoonotic protozoan parasites (closely related both morphologically and genetically to Trypanosoma) that are usually transmitted by biting sand flies and are widely distributed through both tropical and temperate regions of the world. Leishmaniasis is also associated with high levels of morbidity and mortality (Svobodová et al. Reference Svobodová, Votýpka, Nicolas and Volf2003; Gramiccia and Gradoni, Reference Gramiccia and Gradoni2005; Peacock, Reference Peacock2010). Over 40 mammal species are known to harbour Leishmania spp., including cats and rats, with the black, or ‘ship’ rat (Rattus rattus), increasingly recognized as an important natural reservoir in Leishmania transmission (Oliveira et al. Reference Oliveira, Pirmez, Pires, Brazil and Pacheco2005; Quinnell and Courtenay, Reference Quinnell and Courtenay2009; Sherry et al. Reference Sherry, Espinosa, Furlanello, Miranda, Miro, Montoya, Ribas, Solano-Gallego and Trotta2011). In Australia to date, eight novel Trypanosoma spp. have been identified in native wildlife (Paparini et al. Reference Paparini, Irwin, Warren, McInnes, de Tores and Ryan2011; Thompson et al. Reference Thompson, Botero, Wayne, Godfrey, Lymbery and Thompson2013, Reference Thompson, Godfrey and Thompson2014), and leishmaniasis has been reported in macropods in the Northern Territory (Rose et al. Reference Rose, Curtis, Baldwin, Mathis, Kumar, Sakthianandeswaren, Spurck, Low Choy and Handman2004) and is thought to be transmitted by biting midges (Dougall et al. Reference Dougall, Alexander, Holt, Harris, Sultan, Bates, Rose and Walton2011). It is not known whether these endemic parasites can infect feline or rodent hosts.
On Christmas Island (CI), the extinction of two native rat species has been attributed to infection with Trypanosoma lewisi, thought to have been introduced with black rats during incursions by sea-faring traders during the late 19th century (Durham, Reference Durham1908; Andrews, Reference Andrews1909). The observations of these early researchers appears to have been supported recently by Wyatt et al. (Reference Wyatt, Campos, Gilbert, Kolokotronis, Hynes, DeSalle, Daszak, MacPhee and Greenwood2008) who detected T. lewisi DNA in skin samples from two out of six (33.3%) museum specimens of the now-extinct Maclear's rats (R. macleari), and one out of six (16.7%) black rats collected by Durham at the time of European colonization of the island (Wyatt et al. Reference Wyatt, Campos, Gilbert, Kolokotronis, Hynes, DeSalle, Daszak, MacPhee and Greenwood2008). More recently, speculation that trypanosomes were still present on CI was based on the observational finding of Trypanosoma/Leishmania-like organisms in a blood smear of a rat on the island (Hall et al. Reference Hall, Rose, Spratt, Harlow, Donahoe, Andrew, Field, DeJong, Smith and Hyatt2011). Additionally, Trypanosoma spp. infections have been implicated in the precipitous decline of the woylie (Bettongia penicillata) on mainland Western Australia (Smith et al. Reference Smith, Clark, Averis, Lymbery, Wayne, Morris and Thompson2008; Averis et al. Reference Averis, Thompson, Lymbery, Wayne, Morris and Smith2009), although the distribution and prevalence of trypanosome and Leishmania species in Western Australia is not well described.
As part of a larger research study into the effects of introduced species on wildlife in Australia and its islands, tissue samples from feral cats and black rats living on CI, Dirk Hartog Island (DHI) and in southwest Western Australia (swWA) were examined for the presence of Trypanosoma and Leishmania DNA. These locations represent areas of importance for wildlife conservation as well as for public health.
METHODS
Study locations
Samples were collected from three geographically and climatically distinct locations; from CI, mainland swWA, and DHI. CI is an Australian Territory, located in the Indian Ocean (10°29′S, 105°38′E) approximately 360 km south of the Indonesian capital, Jakarta, with a tropical climate. The swWA is a large ecoregion, located south of a line from Geraldton (28°46′28″S, 114°36′32″E) to Esperance (33°51′40″S, 121°33′31″E) with a Mediterranean climate. DHI is an arid inshore island (25°50′S, 113°05′E) located to the west of Shark Bay off the Western Australian coast.
Sample collection
Cat cadavers were collected from CI (n = 35; 8 fresh and 27 frozen), DHI (n = 23; all frozen) and swWA (n = 58; all frozen). Cats from CI and DHI were sourced from the Department of Parks and Wildlife (Parks and Wildlife) management programmes and cats from swWA were obtained during community-coordinated culling programs from 12 locations. Rats (n = 48; 23 fresh and 25 frozen) were collected from CI concurrently with the cats. Spleen samples were collected at necropsy and preserved in 70% ethanol.
DNA extraction
DNA was extracted from cat and rat spleen tissue using the Qiagen spin columns for blood and tissue kit according to the manufacturer's instructions (Qiagen, USA). Negative controls were used in the PCRs with the inclusion of PCR grade water in place of genomic DNA.
PCR conditions – Trypanosoma
The nested PCR protocol from Botero et al. (Reference Botero, Thompson, Peacock, Clode, Nicholls, Wayne, Lymbery and Thompson2013) was employed with generic Trypanosoma primers of the 18S region which have been previously described (Maslov et al. Reference Maslov, Lukeš, Jirku and Simpson1996; McInnes et al. Reference McInnes, Hanger, Simmons, Reid and Ryan2011). External primers used were SLF (5′-GCT TGT TTC AAG GAC TTA GC-3′) and S762 (5′-GAC TTT TGC TTC CTC TAA TG-3′) and internal primers were S823F (5′-CGA ACA ACT GCC CTA TAC GC-3′) and S662R (5′-GAC TAC AAT GGT CTC TAA TC-3′). Cultured Trypanosoma cruzi and T. lewisi were used as positive controls.
PCR conditions – Leishmania
Subsamples of spleens were tested for Leishmania spp. from CI samples only, feral cats (n = 10) and black rats (n = 45), with genus-specific primers adapted from Schönian et al. (Reference Schönian, Nasereddin, Dinse, Schweynoch, Schallig, Presber and Jaffe2003). Primers were from the internal transcriber region (ITS1), OL1853 (5′-CTG GAT CAT TTT CCG ATG-3′) and OL1854 (5′-TGA TAC CAC TTA TCG CAC TT-3′).
A touchdown PCR was performed on all samples using 3 µL of DNA (at 5 ng µL−1) in an 11.5 µL reaction. The reaction contained 1 × buffer, 3.0 mm MgCl, 0.5 mm dNTPs, 0.05 m Betaine, 0.05 µL Taq/Taq Gold and 10 µ m of each primer. PCR cycling conditions were optimized under the following conditions: 1 denaturation cycle at 94 °C for 5 min (Taq)/10 min (Taq Gold) followed by 94 °C for 20 s, 63–56 °C for 60 s using 0.5 °C cycle−1 increments and 72 °C for 60 s. This was then followed by 20 cycles of 94 °C at 20 s, 56 °C for 60 s, 72 °C for 60 s and a final extension of 72 °C for 5 min (Blackwell Laboratory, Australia). Positive controls included DNA extracted from Leishmania major, L. braziliensis, L. tropica, L. donovani and L. australiensis. All PCR products were run on a 1.5% agarose gel at 120 V for 1 h for visualization.
Statistical analysis
Confidence interval values were calculated using the exact binomial methods (Graat et al. Reference Graat, Frankena, Bos, Noodhuizen, Frankena, van der Hoofd and Graat1997).
RESULTS
No Trypanosoma spp. were detected by PCR in any of the spleen samples (Table 1). Positive controls for T. cruzi and T. lewisi amplified at the correct product size and no amplification was detected within the negative control. Similarly, no Leishmania DNA was detected in either cat or rat spleen samples (Table 1). All Leishmania-positive controls produced amplified products at their corresponding sizes, whilst all negative controls did not produce amplification.
Prevalence (%) and 95% confidence interval for Trypanosoma and Leishmania in cats and rats from three geographical regions.
swWA, southwest Western Australia; DHI, Dirk Hartog Island; CI, Christmas Island.
DISCUSSION
This study was conceived when the opportunity arose to sample cats and rats on CI after recent observations on pathology specimens suggested that Trypanosoma spp. may persist in this confined habitat where historical records had putatively incriminated trypanosomiasis for the extinction of two native rodents. We were also interested to investigate whether Trypanosoma DNA could be detected in the blood of introduced animals in regions where trypanosomiasis appears to be endemic in native marsupials upon which they undoubtedly prey. However, we found no evidence of infection with Trypanosoma spp. in feral cats from three geographical locations or black rats on CI. Additionally, there was also no evidence of infection by Leishmania spp. in feral cats or black rats on CI. These results suggest that cats and rats are not currently acting as reservoirs for trypanosomes or Leishmania in these locations, and questions whether Trypanosoma infection persists in any form on CI.
The challenge presenting molecular research when pathogen DNA is not detected in any samples is to justify that target DNA was not missed due to inhibitors and/or suitability of the tissue for that particular work. We are confident that the samples used in this study yield viable DNA as these same samples were screened successfully for the presence of other blood-borne pathogens by molecular methods (e.g. Bartonella species; Dybing et al. (Reference Dybing, Jacobson, Irwin, Algar and Adams2016)), thus ruling out the presence of inhibitors.
Regarding the suitability of tissues used, the spleen is regarded as a reliable location for detecting numerous different blood-borne pathogens, including Trypanosoma, for reasons including; the spleen is the blood filtering organ so pathogens circulating in the blood would be expected to be present (Mebius and Kraal, Reference Mebius and Kraal2005); sampling from the spleen was more sensitive than blood for detecting vector and blood-borne pathogens including trypanosome and ehrlichial infections (Albright and Albright, Reference Albright and Albright1991; Harrus et al. Reference Harrus, Kenny, Miara, Aizenberg, Waner and Shaw2004), and; the primers used in this study have been previously demonstrated/proven to detect trypanosomes in both blood and tissue samples (McInnes et al. Reference McInnes, Hanger, Simmons, Reid and Ryan2011; Botero et al. Reference Botero, Thompson, Peacock, Clode, Nicholls, Wayne, Lymbery and Thompson2013). The nested Trypanosoma PCR primers used in this study provide a highly sensitive methodology for detecting low DNA concentrations in tissues (McClatchey, Reference McClatchey2002). Very low levels of DNA are highly likely to amplify when using nested PCR primers, compared to conventional single step PCR, as two primer pairs are required to amplify a target sequence and there is a decrease in non-specific banding (McClatchey, Reference McClatchey2002; Pardo and Pérez-Villareal, Reference Pardo and Pérez-Villareal2004). Although the sensitivity of these primers has not been calculated for tissue, it has been calculated for blood (Dunlop et al. Reference Dunlop, Thompson, Godfrey and Thompson2014). Given that Dunlop et al. (Reference Dunlop, Thompson, Godfrey and Thompson2014) calculated that use of these primers and amplification conditions in blood with >74 parasites/0.3 mL had a detection sensitivity of >80%, it is extremely likely that even low levels of parasitaemia would be detected in spleen samples.
Whilst the possibility of missing the presence of either Trypanosoma or Leishmania occurring at very low levels of parasitaemia cannot be discounted, we do feel confident that the PCR protocol used would detect even low levels of parasitaemia in our samples. For the scope of this paper though, quantification of parasitaemia (intensity) was not considered as important as the presence/absence of Trypanosoma or Leishmania species.
Unfortunately serum samples were not available for rats or cats in this study; serological testing may have provided additional information regarding exposure (or otherwise) of the hosts to these parasites and should be considered for future investigations.
Whilst cat and rat spleen samples were sourced from a focal area on CI, specifically from around the town site, this was representative of the initial sampling area utilized by Durham (Reference Durham1908). Additionally, the relatively small size of this island (135 km2) suggests that Trypanosoma and Leishmania would have expected to have been identified in our samples if they were circulating within the rat and cat populations. Assuming a prevalence of at least 10%, the probability of missing a positive animal is 0.006 (0.6%) based on the sample size of 48 rats used in this study.
The only samples tested by Wyatt et al. (Reference Wyatt, Campos, Gilbert, Kolokotronis, Hynes, DeSalle, Daszak, MacPhee and Greenwood2008) from before black rat introductions to CI were from the bulldog rat (R. nativitatis; n = 3), with PCR failing to detect any trypanosomes. Therefore it is not possible to confirm the presence or absence of T. lewisi on CI prior to black rat introduction (Wyatt et al. Reference Wyatt, Campos, Gilbert, Kolokotronis, Hynes, DeSalle, Daszak, MacPhee and Greenwood2008). However, if T. lewisi was endemic on CI in the native Maclear's and bulldog rats before black rat introduction, then it could be hypothesized that it was similarly lost along with the demise of the native rats.
Based on the findings of this study, the link between black rats as the source of the Trypanosoma spp. on CI is tenuous considering the hypothesized host (black rats), intermediate host (Xenopsylla cheopis; Hoare (Reference Hoare1972)) and a mechanical vector (Polyplax spinulosa; Khachoian and Arakelian (Reference Khachoian and Arakelian1978)) are still present on the island (unpublished results), whilst our efforts to detect the presence of any Trypanosoma spp. was not successful. If T. lewisi introduced with black rats has resulted in, or at least contributed to, the extinction of two endemic rodent species, then it would not be unreasonable to expect T. lewisi to still be present in these hosts today.
Whilst rodent (rat and mice) trypanosomes have been studied, there is still a paucity of information in Australia. Exotic trypanosomes found in native rodents include T. lewisi from the bush rat (25%); a species genetically similar to T. lewisi in the ash-grey mouse (50%); and an unknown Trypanosoma spp. in the Shark Bay mouse (16.7%) (Averis et al. Reference Averis, Thompson, Lymbery, Wayne, Morris and Smith2009). Introduced rodents infected with T. lewisi in Australia include the house mouse, brown rat and the black rat (Mackerras, Reference Mackerras1959). Several novel Trypanosoma spp. have been identified in a range of Australian native wildlife species (Smith et al. Reference Smith, Clark, Averis, Lymbery, Wayne, Morris and Thompson2008; Austen et al. Reference Austen, Jefferies, Friend, Ryan, Adams and Reid2009; Averis et al. Reference Averis, Thompson, Lymbery, Wayne, Morris and Smith2009; Paparini et al. Reference Paparini, Irwin, Warren, McInnes, de Tores and Ryan2011). Indeed, Trypanosoma spp. have been implicated in the demise of marsupial populations in swWA (Smith et al. Reference Smith, Clark, Averis, Lymbery, Wayne, Morris and Thompson2008; Averis et al. Reference Averis, Thompson, Lymbery, Wayne, Morris and Smith2009).
In Australia, there is an absence of research into trypanosomes from cats however, natural and experimental infections of multiple species of Trypanosoma have been found in felines from other countries including; T. brucei, T. cruzi, T. evansi and T. rangeli. Experimental infections in cats have also been reported for T. congolense and T. gambiense. Trypanosoma cruzi is the most widely reported species occurring in cats with most cases originating from Latin America and prevalences ranging from 2.9 to 63.6% (Zeledón et al. Reference Zeledón, Solano, Burstin and Swartzwelder1975; Mott et al. Reference Mott, Mota, Sherlock, Hoff, Muniz, Oliveira and Draper1978; Wisnivesky-Colli et al. Reference Wisnivesky-Colli, Gürtler, Solarz, Lauricella and Segura1985). However, many indigenous Australian mammal species are thought to be susceptible to infection by exotic Trypanosoma species if they were to establish in Australia (Thompson, Reference Thompson2013). The absence of trypanosome infection in cats sampled from swWA and DHI suggests that cats are not a major reservoir species in these areas and therefore may not contribute to trypanosome persistence in the environment.
Domestic cats and black rats have been identified as sources of infection of the pathogenic zoonosis caused by Leishmania infantum (Poli et al. Reference Poli, Abramo, Barsotti, Leva, Gramiccia, Ludovisi and Mancianti2002; Quinnell and Courtenay, Reference Quinnell and Courtenay2009; Maia and Campino, Reference Maia and Campino2011). At the time of this study a significant proportion of the CI population was transitory and originated from diverse geographic locations, including many areas where Leishmania is endemic. However, we found no evidence of feral cats or black rats acting as reservoirs for Leishmania spp. on CI.
CONCLUSIONS
This study found no evidence of Trypanosoma spp. infection in cats and black rats from three geographically distinct locations. Of particular interest is the absence of trypanosomes from black rats on CI given that T. lewisi has previously been reported as occurring in rats and other rodent hosts on the island, and has been hypothesized as contributing to the extinction of two endemic rodent species. Previous studies have implicated Trypanosoma spp. in fauna decline; however, in the case of CI, the findings of this study do not readily support this hypothesis. This study also found no evidence of feral cats or black rats harbouring Leishmania spp. on CI.
ACKNOWLEDGEMENTS
The authors would like to acknowledge Neil Hamilton from Parks and Wildlife and Michael Deller for sample collection from Dirk Hartog Island and Christmas Island as well as the farmers and the Red Card for Rabbits and Foxes programme for feral cat collection in the southwest WA. The authors would also like to acknowledge Adrian Wayne from Department of Parks and Wildlife for sample collection in the southwest WA. We would also like to thank the staff of Christmas Island National Parks for their assistance during this project providing a place to perform laboratory work. The Department of Immigration and Citizenship kindly provided accommodation during field collections. We appreciate the support received from Christmas Island Phosphates and would like to acknowledge support and encouragement from the community of Christmas Island and for allowing us to work around their properties. The authors would also like to acknowledge Chris Peacock and Ace Choo for guidance with the Leishmania analysis and Adriana Botero for guidance with the Trypanosoma analysis.
FINANCIAL SUPPORT
This work was completed as part of Narelle Dybing's PhD project with supporting funds provided by the Department of Parks and Wildlife (DPaW) as well as Murdoch University and the Murdoch University Veterinary Trust's Weston Fernie Research fund.
CONFLICT OF INTEREST
None.
ETHICAL STANDARDS
The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional guides on the care and the use of laboratory animals.
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