MEM INST OSWALDO CRUZ, RIO DE JANEIRO, 92(3) May/Jun 1997
PAGES: 357-358 DOI: Technical notes
Morphological and Biometrical Differences among Trypanosoma vivax Isolates from Brazil and Bolivia

AMR Dávila +, L Ramirez, RAMS Silva

Laboratório de Ecopatologia, Centro de Pesquisa Agropecuária do Pantanal, EMBRAPA, Rua 21 de Setembro 1880, 79320-900 Corumbá, MS, Brasil

RESEARCH NOTE

Trypanosoma vivax, originating in Africa, has been found in Central America, South America, the West Indies and Mauritius (ND Levine 1973 Protozoan Parasites of Domestic Animals and of Man, Burgess Publishing Company, Minneapolis, Minessota, 406 pp.). T. vivax was reported in the New World for the first time in French Guyana (M Leger & M Vienne 1919 Bul Soc Pathol Exotique 12: 258-266) and later in other parts of South America, Central America, and some Caribbean islands (RD Meléndez et al. 1995 Trypnews 2: 4). JJ Shaw and R Lainson (1972 Ann Trop Med Parasitol 66: 25-32) made the first record of T. vivax in Brazil when they recorded its presence in a water buffalo (Bubalis bubalis) from the vicinity of the city of Belém and cattle and sheep elsewhere in the State of Pará. RAMS Silva et al. (1996 Mem Inst Oswaldo Cruz 5: 561-562) reported the first occurence of T. vivax in the Pantanal region of Brazil on the border with Bolivia and in the same year this parasite was found in Bolivia (RAMS Silva et al. Vet Parasitol submitted).

In the present study we compared measurements of T. vivax in blood-films from naturally infected bovines from Brazil and Bolivia. According to CA Hoare (1972 The Trypanosomes of Mammals. A Zoological Monograph, Blackwell Scientific Publication, Oxford, 749 pp.) the range of lengths of T. vivax is from 18 µm to 31 µm (including free flagellum 3-6 µm long) with means from 21 µm to 25.4 µm, while over 90% of the measurements are between 20 µm and 26 µm. Biometrical studies of isolates from Pantanal (Brazil) and Santa Cruz (Bolivia) were carried out as described by RAMS Silva et al. (1995 Vet Parasitol 60: 167-171) in 100 and 80 observations from thin smears of each isolate, respectively. In each case, five sets of smears were taken from isolates for the biometrical study. The data were analyzed statistically using a T-test. The difference in length among isolates from the Pantanal (18.73 µm), Pará (22.77 µm) reported by Shaw and Lainson (loc. cit.) and Bolivia (15.86 µm) were highly significant (p<0.001). Based on CA Hoare and JC Broom (1938 Trans R Soc Trop Med Hyg 31: 517-534) the size of Bolivian isolate is out of the normal range and could be a sufficient criteria to classify it as T. uniforme. The biometrical differences were highly significant between isolates and only the distance from kinetoplast to posterior end between Bolivian and Brazilian (Belém) parasites and the distance from kinetoplast to nucleus between Brazilian trypanosomes were not significant (Table). These results show that there is a similarity in the subterminal position of kinetoplast among Brazilian (Belém) and Bolivian parasites and all three isolates are biometrically different among bovines species from Brazil and Bolivia.

The body of the Santa Cruz parasite at the rounded posterior end was more broad than that of the Poconé trypanosome (Figs 4, 5, 6). However, the Poconé parasite was more tapered than the Santa Cruz toward the anterior and posterior end (Figs 1, 2, 3). The kinetoplast of the Poconé parasite was more oval than that of the Santa Cruz. In the former, the kinetoplast was lateral and subterminal and in the latter it was more terminal. The free flagellum of Bolivian trypanosome was shorter than that of the trypanosomes from Poconé and Belém. The nucleus of the Bolivian parasite was bigger and more rounded than that of the Poconé (Figs 4, 6). H Fairbairn (1953 Ann Trop Med Parasit 47: 394-405) showed that short forms were characteristic of the strain causing acute disease in cattle of West Africa, while long forms are associated chiefly with strains causing chronic infection in East Africa. As recent studies by RAPD (Random Amplified Polymorphic DNA) analysis showed that South American T. vivax originated from West Africa (MF Dirie et al. 1993 J Euk Mircrobiol 40: 132-134), we believe that shorter forms reported in this work could be related with the acute disease observed by us here and Fairbairn in West Africa (loc. cit.). In the recent past, authors as Shaw and Lainson (loc. cit.) reached the same conclusion with regards the Belém parasite of the water buffalo. 

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