The present study analyzed results of coproparasitological exams from 13 species of Felidae kept in captivity and from feral domestic cats that are circulating in São Paulo Zoo; this was performed over a period of 4 years beginning January/2009 and ending December/2012, and included all samples received by the Clinical Analysis Laboratory. As a general protocol followed by this institution, fresh fecal samples were obtained from the animal enclosure, using clean, uncontaminated material and all samples were processed through the following techniques: direct method, fecal flotation with sodium chlorite solution and fecal sedimentation. The smears were analyzed under optical microscopy and the parasite identification was performed according to morphological characteristics using the literature available [39] [40]. Captive species were divided into native and exotic, depending on the current distribution and native location of studied species, according to IUCN Red List of Threatened Species online database.

This retrospective study analyzed 587 results of processed samples from 13 captive species and 27 results from feral cats. To make the survey more accurate and safer, only the data that presented parasite identification in the minimum level of genus was used. This resulted in a total of 541 samples of captive animals and 27 of feral domestic cats.

After initial screening, three different types of analysis were performed: comparison between results of native and exotic felids; prevalence of infections in feral domestic cats and analyses of all felid captive species in the FPZSP. The analyses were performed quantitatively, based on the percentage of samples that showed positive results for a given parasite.

These analyses allowed us to identify which parasites were most frequently found in each group (native felids, exotic felids, captive felids in general and wandering domestic cats), compare the results among these groups and identify the parasite that is most commonly found in each species.

Among 541 results analysed, 105 (19.41%) were positive for at least one parasite. Mixed infections were found in two samples from Leopardus colocolo and in both of them protozoa Isospora sp. and Eimeria sp. were associated. Samples indicating the presence of helminths corresponded to 16.63% (90/541), while 3.14% (17/541) were positive for protozoans. The results show that helminth infections are more frequent than protozoan infections in both native, 14.78% (51/345), and exotic species, 19.9% (39/196).

Considering felids in general, Toxocara cati was the helminth with the highest prevalence with 43 (7.95%) positive samples, followed by Toxascaris leonina with 41 (7.58%) positive samples, Hymenolepis nana with five (0.92%), and Ascaris sp. with only one (0.18%). Among protozoans, Isospora sp. was the most common, with 11 (2.03%) positive samples; Eimeria sp., Giardia sp. and Blastocystis sp. were the second most frequent with two (0.37%) positive samples each (Table 1).

From the 541 results analyzed, 345 (63.77%) were referring to the native species, while 196 (36.22%) were related to the exotic species.

Considering only native species samples, 80.87% (279/345) were negative and 19.13% (66/345) were positive for any parasite. The most frequent parasite found in this group was T. cati, found in 43 (12.46%) samples, followed by Isopora sp. (3.19%), T. leonina (1.74%), Eimeria sp. (0.58%), Giardia sp. (0.58%), Blastocystis sp. (0.58%) and H. nana (0.58%) (Table 2). Considering only positive results, Toxocara cati was found in 65.15% of the samples, followed by Isopora sp.

n = number of positive samples.

(16.67%), T. leonina (9.09%), Eimeria sp. (3.03%), Giardia sp. (3.03%), Blastocystis sp. (3.03%) and H. nana (3.03%).

All native felids were positive for at least one parasite, except for ocelot (Leopardus pardalis) and jaguar (Panthera onca), which had negative results. The only parasite found in margay (Leopardus wiedii) was the helminth belonging to the class Cestoda, H. nana. The protozoans Eimeria sp. and Blastocystis sp. were identified only in pampas cat (Leopardus colocolo) and geoffroyi’s cat (Leopardus geoffroyi) samples, respectively (Table 2).

Samples related to exotic species, from 196 results analyzed, 157 (80.1%) were negative for the presence of parasites and 39 (19.9%) were positive. In this group, Toxocara leonina had the highest prevalence, found in 35 (17.86%) samples. Hymenolpis nana was the second most prevalent with 1.53% (3/196), followed by Ascaris sp. found only in one sample (0.51%) (Table 2). Considering positive samples, Toxocara leonina was the most common parasite (89.74%), followed by H. nana with 7.69% and Ascaris sp. with 2.56%. All samples were negative for protozoan and T. cati infections. Although the prevalence was high for T. leonina, this parasite was found in only two species, Panthera leo and Panthera tigris tigris. Hymenolepis nana and Ascaris sp. were identified in only in Leopardus serval and P. tigris, respectively. All samples of leopard (Panthera pardus mela) and amur tiger (P. tigris altaica) were negative (Table 2).

Among all analyzed samples, T. cati had the highest prevalence (7.95%), where it was identified in 43 samples. The second most common was T. leonina found in 35 samples (7.58%), followed by Isospora sp. with prevalence of 2.03% (11/541), H. nana found in five samples (0.92%), Eimeria sp., Giardia sp. and Blastocystis sp. found in two samples and with a prevalence of 0.37% each and Ascaris sp. identified in only one sample (0.18%) (Table 1). Considering only positive samples, T. cati had a prevalence of 40.95%. The second most common was T. leonina (39.05%), followed by Isospora sp. (10.48%), H. nana (4.76%), Eimeria sp., Giardia sp. and Blastocystis sp. (1.90% each) and Ascaris sp. (0.95%).

Toxocara cati was the most common parasite in this study, but it was present only in native animal samples, while Ascaris sp. appeared only in exotic animals. Some species did not have parasite infections, these were: ocelot (L. pardalis), jaguar (P. onca), leopard (P. pardus mela) and amur tiger (P. tigris altaica) (Table 2).

Twenty-seven coproparasitological exam results were analyzed, of which seven (25.93%) showed negative results and twenty (74.07%) were shown to be positive for at least one parasite species. Mixed infections were identified in six samples (22.22%) and the most frequent association was between T. cati and Giardia sp. in four samples (14.81%) (Table 3).

Samples from this group showed that infections by helminths were more common than for protozoans. Helminths were present in 16 samples (59.26%) and protozoans in nine (33.33%) (Table 3). Three different parasite species were identified: T. cati, in 16 samples (59.26%), followed by Giardia sp. in six samples (22.22%) and Isospora sp. in three samples (11.11%) (Table 3). Considering only positive samples, T. cati appeared in 80% of samples, followed by Giardia sp. in 30% and Isospora sp. identified in 15%.

The present study found a prevalence of parasitic infection in captive animals of 19.41%. This prevalence was lower than has previously been reported in Brazil, with prevalence ranging from 20.2% to 64.3%, and other studies conducted around the world, which reported infection rates between 36.7% and 89.3% [17] [18] [28] [29] [35] [38]. Although some studies included other Carnivora species, if only felids are considered, the prevalence is still higher than the one observed in the present study [17] [18] [28] [29] [35] [38]. This is probably due to the adoption of careful sanitary measures, including frequent cleaning of enclosures, removal of food debris and use of footbaths, all accepted preventive veterinary medicine techniques [35] [41].

The prevalence of helminth infections (16.63%) in the present study was higher than that of protozoan (3.14%), a fact also observed in zoos in Malaysia, Bangladesh and Italy [17] [28] [35].

Considering the coproparasitological profiles, T. cati was reported as one of the most common parasites in felids, not only in Brazil, but also around the world [38]. Our study corroborates that, with this being the parasite with the highest prevalence. This demonstrates the cosmopolitan characteristic of this parasite, the resistance of its eggs and its infective capacity [28] [35] [41] [42]. These infections were already observed in several reports [17] [27] [32] [35] [38]. The striking presence in lions (P. leo) confirms the findings in India and Italy [32] [35]. The results in the northern tiger (L. tigrinus) confirm the finding in Paraná (Brazil) [38]. The existence of T. leonina in bengal tiger (P. tigris tigris) differs from previous findings, where T. cati predominated [17] [28] [35]. The frequent presence of T. leonina in captive animals and absence in wild cats is frequently reported in the literature, a fact that could be explained by the difference of food offered to captive lions and the proximity of these animals to a great variety of other host species [30]. It is also known that the life cycle of this parasite greatly influences the persistence of infections since its eggs become infective on the soil in one week, facilitating the contamination of captive animals [42].

Isospora sp. was found in four species in a relatively low prevalence (2.03%), when compared to another study realized in Paraná, Brazil, that was of 14.28% [38]. Despite the low prevalence, the presence of this parasite in captive animals may represent a risk, since stress or other infection may lead to development of main symptoms of isosporosis [43].

The low prevalence of H. nana (0.92%), Eimeria sp. (0.37%), Blastocystis sp. (0.37%) and Ascaris sp. (0.18%) found in this study corroborates with other studies [36]. Eimeria sp. was not reported as infecting felids, however some studies did not specify the coccidian genera found in their studies [17] [30]. Blastocystis sp. was found only in geoffroyi’s cat (L. geoffroyi), the literature reports the presence of this parasite only in primates [28]. Ascaris sp. was present only in bengal tiger (Panthera tigris tigris); this parasite has been reported to exhibit high prevalence in herbivores [18].

The prevalence of Giardia sp. (0.37%) was low when the present study is compared to others [29] [30]. Presence of Giardia sp. was already reported in other zoos, mainly in Brazilian native species [29] [44].

Among the 13 captive species analyzed in this study, only four had negative results for all samples: ocelot (L. pardalis), jaguar (P. onca), leopard (P. pardus mela) and amur tiger (P. tigris altaica). The small number of samples of ocelot and leopard could be one of the reasons for these findings. The results observed for jaguar are different from those found in other studies that report infections by helminths and protozoans [29] [38]. Amur tigers were already found to have parasite infections in eastern Russia [45].

Spirometra sp. is a common helminth in zoological animals, constantly found in felids and is considered the most frequent parasite in some studies [17] [28] [30] [31] [37] [38]. The absence of this cestode in samples from FPZSP could be attributed to the absence of intermediate hosts necessary for completing the parasite life cycle [17] [41].

The difference between coproparasitological profiles of native and exotic species is considerable regarding the number of parasite species and prevalence. Among native felids, seven parasite species were identified: T. cati (12.46%), Isospora sp. (3.19%) and Toxascaris leonina (1.74%). Among the exotic felids, only three species were observed: T. leonina (17.86%), H. nana (1.53%) and Ascaris sp. (0.51%). A similar occurrence was observed in Pomerode Zoo (Santa Catarina, Brazil), where all exotic felids were free of gastrointestinal parasite infections, while native species had infections by Giardia sp. and Trichuris sp. [29].

Although the parasite species infecting the two groups were different, infection rates were similar. Among the native samples, 19.13% were positive to parasites, compared to 19.9% of exotic species samples. In addition, helminths were the most frequent infections in both groups, representing 14.78% of native samples and 19.9% of exotic samples.

In the present study, an infection rate of 74.07% was observed in Felis catus samples, much higher than the prevalence reported for domiciled cats, where prevalence ranged from 31.5% to 56.8% [14] [15] [21] [24] [25]. However, it was lower when compared to the prevalence obtained by studies with wandering cats, that was of 87.9% and 100% [19] [24].

Multiple parasitism was observed in 22.22% of the samples, and association between T. cati and Giardia sp. was the most frequent. Previous studies in Rio de Janeiro (Brazil)reported associations between Ancylostoma sp. and Toxocara sp. in 32.8% of samples [24].

Considering the coproparasitological profile of these animals, three species were identified, a lower diversity than reported by other authors when six to nine species were identified [14] [15] [19] [21] [25].

In the present study, helminth T. cati was the most common, with a prevalence of 59.26%; similar results were obtained in other cities in São Paulo state [19] [23]. However, there was a big difference from other studies with wandering and domiciled cats, in which T. cati appears with a prevalence ranging from 0.86% to 19.1% [14] [15] [20] [21] [24] [25]. One explanation for this low prevalence in domiciled animals is due to good nutrition and periodic antiparasitic treatment. The low values reported in other studies with wandering animals may reflect the lack of fixed habitat of these cats, since the eggs of T. cati need four weeks to reach the infecting stage, a time surpassing to the presence of the animals [42].

Despite other studies presenting greater infection by protozoa [21], in this study, Giardia sp. had a prevalence of 22.22% and is the second most prevalent parasite. Although there was a similar result in Botucatu (São Paulo, Brazil), a lower prevalence is commonly reported in the literature [15] [19] [21] [24] [25]. This parasite affects not only companion animals, but also other mammals, including humans. This parasite is considered to have zoonotic potential, causing severe enteritis, so understanding its distribution among animals that share the same environment with humans is essential for our health [38] [42].

While the present study reports a low prevalence of Isospora sp. (11.11%), other studies found it to have higher prevalence between 45.3% - 50.72%, and being the most common parasite [23] [24] [25].

It is important to highlight the absence of Ancylostoma sp. in the studied population, a parasite commonly mentioned in studies with domestic cats [19] [24]. It is suggested that the absence of this parasite is due either to non-infection or the fact that cats are still not releasing eggs of hookworms in their feces.

Although the number of identified parasite species in the captive felids samples was higher than those of feral felids, the same parasites were found in both groups but in different prevalence. Toxocara cati had the highest prevalence in both feral and captive groups. Giardia sp. was the second most common parasite among feral cats (22.22%), however its prevalence was significantly lower (0.37%) in the captive group. Isospora sp. was the third most common in both captive and feral animals, but more frequent among feral cats than captive (11.11% and 2.03%, respectively). While these shared species are significant, their presence alone is not sufficient evidence to claim that feral cats are their reservoirs. As has been noted, past studies have shown that these parasites are frequently found in felids in general and all species have already been reported for both groups. While the existence of a proximally relevant transmission route between feral and captive felids is legitimate, it does not appear to be the predominant method by which captive felids are acquiring infection. This must, of course, be afforded additional studies and ideally, alternative sampling and analyzing methodologies. Indeed, the authors recognize that the absence of an active sampling methodology was a limitation of this study. Nonetheless, it is hoped the work has provided a foundation for what is needed, and adds to our understanding of the parasitic profile of these animals. Going forward, we also recognize the importance of maintaining control over the feral colonies living in the FPZSP area given their close contact with humans and the potential for disease spread within the community.