Mem Inst Oswaldo Cruz, Rio de Janeiro, 99(6) October 2004
Short communication

Blood and Intestinal Parasites of Squirrels (Rodentia: Sciuridae) in Amazonian Brazil

Ralph Lainson
+, Maria do Carmo de Oliveira Brígido*, Fernando Tobias Silveira

Departamento de Parasitologia, Instituto Evandro Chagas, Av. Almirante Barroso 492, 66090-000 Belém, PA, Brasil
*Instituto Brasileiro do Meio Ambiente e de Recursos Naturais Renováveis, Belém, PA, Brasil

Page: 577-579
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We report the result of an examination for blood and intestinal protozoa in 12 specimens of the red squirrel Sciurus spadiceusu00a0(Rodentia: Sciuridae) from Birroque,u00a0municipality of Plácido de Castro, state of Acre, Brazil. No parasites were detected in thin, Giemsa-stained blood films of the animals, but culture of the blood of three in Difco B45 medium blood-agar slants gave rise to isolates of epimastigotes. Inoculation of one isolate into laboratory mice resulted in the appearance ofu00a0Trypanosoma cruzi-like trypomastigotes in their peripheral blood, and the other two isolates gave rise to transient infections with au00a0T. lewisi-like parasite in inoculated mice and hamsters. The failure of the latter parasite to develop in the triatomine bugu00a0Rhodnius robustus suggests that it is probably notu00a0T. rangeli.u00a0This appears to be the first record of au00a0T. lewisi-like trypanosome in neotropical squirrels. Oocysts of anu00a0Eimeriau00a0sp., were detected in the faeces of 10 animals (83.3%). The parasite develops in the epithelial cells of the intestine, where it may cause severe damage and sometimes results in death of the animal. No oocysts were detected in bile.

During 2001-2002, a parasitological study was made of 12 specimens of the red squirrel Sciurus spadiceuscaptured along the AC 40 Highway, km 70, in the locality of Birroque, municipality of Plácido de Castro, state of Acre, North Brazil. Blood was obtained from the femoral vein of the animals for preparation of thin blood films and culture in Difco B45 medium blood-agar slants. Air-dried blood films were fixed in absolute methyl alcohol and stained by Giemsa's method. Cultures were checked at weekly intervals and only discarded if negative at one month.

Faecal samples from the squirrels were lightly triturated in 2% aqueous potassium dichromate solution (K2Cr2O7) and spread as a thin layer in covered Petri dishes kept at approximately 24-26ºC. They were examined at once for the presence of coccidial oocysts, using normal light microscopy at magnifications of x 160 and x 400 and then at daily intervals to follow development of any oocysts detected. Bile was removed from the gall bladder of autopsied animals and also examined for oocysts. Tissues for histology were fixed in 10% buffered formol-saline, embedded in paraffin wax and examined in sections cut at 4 µm and stained with haematoxylin and eosin. Photomicrographs were made with a Zeiss "Photomicroscope III" and Kodak TMX 100 film.

No parasites were detected in the Giemsa-stained blood films of the squirrels, but growth of epimastigotes occurred in the cultures of blood from three of them. The culture forms of one isolate were morphologically quite different from those of the other two cultures, and when inoculated into laboratory mice produced trypomastigotes which were morphologically indistinguishable from T. cruzi (Fig. 1).The epimastigotes of the other two cultures were remarkably elongated (Fig. 2) and inoculation of parasites from 10 day-old cultures into mice and hamsters gave rise to infections with a Trypanosoma lewisi-like parasite (Fig. 3). These infections were of a fleeting nature, however, and by the 4th day post-inoculation the trypanosomes had disappeared from the peripheral blood: subsequent attempts to isolate the parasite from the mice following the culture of blood failed.

Initially, morphology of the trypomastigotes led us to suspect that the T. lewisi-like parasite might be T. rangeliand so, on three occasions, batches of approximately 20 nymphs of the triatomine bug Rhodnius robustus were fed on mice which were showing trypomastigotes in their peripheral blood at two days p.i. Dissection of the bugs made at 1, 2, 4, and 6 weeks after the blood-meal showed no development of the parasite in the intestine or the haemolymph.

The type host of T. rangeli Tejera, 1920is the triatomine R. prolixus and natural and experimental infections have also been recorded in a wide variety of other triatomine species (D'Alessandro 1976). R. robustus is very closely related to R. prolixus (Lent & Wygodzinsky 1979), to the extent that doubts have been expressed that they represent two distinct species. Our failure to infect R. robustus with the T. lewisi-like parasite, together with the fact that this insecthas been shown to be a suitable vector of T. rangeli (D'Alessandro-Bacigalupo & Gore-Saravia 1999), therefore leads us to suspect that we are dealing with an-other trypanosome. However, although R. prolixusis known to be susceptible to the majority of T. rangeli strains, reports do exist of the occasional failure to infect this insect with other isolates (Steindel & Guarneri 1996) and this clearly indicates our need to investigate the susceptibility of other species of triatomines.

Our attempts to obtain development of this parasite in the mosquitoes Culex quinquefasciatus and Aedes aegypti, and the phlebotomine sand fly Lutzomyia longipalpis were equally unsuccessful. As fleas are vectors of T. lewisi of rats, and highly suspected to transmit species of T. lewisi-like typanosomes of squirrels in the Old World (Hoare 1972), they may well be vectors of the trypanosome in S. spadiceus.

In his treatise on the trypanosomes of mammals, Hoare (1972) listed the known species within the subgenusHerpetosoma and drew attention to the fact that although T. lewisi-like trypanosomes had been described in North American sciurids (Dorney 1967), there was no record of a similar parasite in neotropical squirrels. We, too, have been unable to trace any such report.

Oocysts of an Eimeria sp., all with similar morphology (Fig. 4 ) were detected in the faeces of 10 (83.3%) of the squirrelsexamined for coccidial parasites. A few fully sporulated oocysts were seen, at autopsy, in stained smears of the ileum of a heavily infected animal but sporulation of the majority was only completed at some time within 24 h outside the host; no oocysts were found in the bile of two infected animals that were autopsied.

Endogenous stages developed in the epithelial cells of the small intestine, with massive infections resulting in extensive desquamation of the gut epithelium (Figs 56) and sometimes in death of the animal. Such infections may have been exacerbated by the stress of captivity. This coccidian of Brazilian squirrels is of interest in confirming the severity of coccidiosis in the genus Sciurus, previously noted in the squirrel S. aureogaster hypo-pyrrhus from Belize, Central America (Lainson 1968) and as discussed by Pellérdy (1974).

The taxonomic status of both the T. lewisi-like and T. cruzi-like trypanosomes is at present speculative, but it is hoped that continuing studies will provide information on the reproductive phase of their life-cycles and biochemistry which will indicate the parasites' affinities and permit their full descriptions. Depository numbers of two specimens of S. spadiceus are 33535 and 33536.

The present study was carried out within the project "Coccidia and trypanosomatids of the Amazonian fauna of Brazil: taxonomy and life-cycles" approved by the Ethics Committee of the Instituto Evandro Chagas. The sub-project "Protozoal parasites of squirrels (Sciurus spp.)" has been approved by the Brazilian Institute for the Environment and Natural Resources (Ibama), Belém.



To Dr Sebastião A da Silva Valente for provision of laboratory-bred Rhodnius robustus and Aprigio N de Lima and Antonio J de Oliveira Monteiro for the maintenance and experimental use of these triatomines. To Domingos M da Souza for invaluable work in the field, and Constância M Franco, Roseli R Braga, Yara LL Jennings, Manoel C de Souza, Iorlando R Barata, Raimundo N Barbosa Pires, and Max Moreira Alves for technical assistance. Dr José de Sousa e Silva Jr., Department of Zoology, Museu Paraense Emilio Goeldi, Belém kindly identified the squirrels.



D'Alessandro A 1976. Biology of Trypanosoma (Herpetosoma) rangeli Tejera, 1920. In WHR Lumsden & DA Evans, Biology of the Kinetoplastida, Vol. I, Academic Press, London, New York, San Fransisco, p. 327-403.

D'Alessandro-Bacigalupo A, Gore-Saravia N 1999. Trypanosoma rangeli. In HM Gilles, Protozoal Diseases, Oxford University Press, Oxford, p. 398-412.

Dorney RS 1967. Incidence, taxonomic relationships and development of lewisi-like trypanosomes in Wisconsin Sciuridae. J Protozool 14: 425-428.

Hoare CA 1972. The Trypanosomes of Mammals,Blackwell Scientific Publication, Oxford, 749 pp.

Lainson R 1968. Parasitological studies in British Honduras III. - Some coccidial parasites of mammals. Ann Trop Med Parasitol 62: 252-259.

Lent H, Wygodzinsky P 1979. Revision of the Triatominae (Hemiptera, Reduviidae), and their significance as vectors of Chagas disease. Bull Amer Museum Natural History, Vol. 163, Article 3, New York.

Pellérdy LP 1974. Coccidia and Coccidiosis, Verlag Paul Parey, Berlin & Hamburg, 959 pp.

Steindel M, Guarneri A A 1996. Interaction of trypanosomes with different triatomine species. Mem Inst Oswaldo Cruz 91 (Suppl.): 32-33.

Tejera E 1920. Un noveau flagellé de Rhodnius prolixusTrypanosoma (ou Crithidiarangeli n.sp. Bull Soc Path Exot 13: 527-530.

+Corresponding author. Fax: +55-91-226.1284.
Received 15 April 2004
Accepted 3 September 2004
Financial support: Ministry of Health, Secretaria de Vigilância em Saúde, Brazil and grant 066445 from the Wellcome Trust, London (FTS and RL)

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