First record of a possible trypanotolerant cattle breed in Latin America: Parasitological, serological, and clinical aspects

被引:0
|
作者
de Mendonca, Debora Ribeiro [1 ]
Couto, Luiz Fellipe Monteiro [1 ]
Pureza, Luana Hernandez [1 ]
Martins, Danieli Brolo [1 ]
Soares, Vando Edesio [2 ]
Ferreira, Lorena Lopes [3 ]
Fioravanti, Maria Clorinda Soares [1 ]
Bastos, Thiago Souza Azeredo [1 ]
da Cunha, Paulo Henrique Jorge [1 ]
Lopes, Welber Daniel Zanetti [1 ,4 ]
机构
[1] Univ Fed Goias, Escola Vet & Zootecnia, Goiania, GO, Brazil
[2] Univ Brasil, Descalvado, SP, Brazil
[3] Univ Fed Minas Gerais, Dept Med Vet Prevent, Escola Vet, Belo Horizonte, MG, Brazil
[4] Univ Fed Goias, Dept Biociencias & Tecnol, Inst Patol Trop & Saude Publ, Goiania, GO, Brazil
关键词
Cattle; Curraleiro Pe<acute accent>-Duro; Packed cell volume; Parasitemia; Trypanosoma vivax; Trypanosomosis; Trypanotolerance; TRYPANOSOMA-VIVAX; AFRICAN TRYPANOSOMIASIS; ANIMAL TRYPANOSOMIASIS; SOUTH-AMERICA; RESISTANCE; STATE; SUSCEPTIBILITY; LIVESTOCK; OUTBREAK; NDAMA;
D O I
10.1016/j.vprsr.2024.101090
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Trypanosoma vivax infections are endemic in Africa, where they provoke trypanosomosis against which some local taurine breeds are tolerant and are thus named trypanotolerant. In Latin America, T. vivax was imported in 1919, since when it has been responsible for periodic outbreaks of the disease. This study assessed whether a South American taurine breed resilient to several parasitic and infectious diseases (Curraleiro Pe<acute accent>-Duro-CPD) can meet trypanotolerant criteria (control parasite proliferation, prevent anemia, survive without treatment, and maintain productivity). Three groups were established, each consisting of six animals (Group 1: CPD-infected; Group 2: Holstein/Gyr-infected; Group 3: Holstein/Gyr-uninfected, negative control). Groups 1 and 2 were infected with T. vivax on Day 0 and evaluated until day 532. Throughout the experimental period, parasitological (Woo and Brener), molecular (cPCR), serological (enzyme-linked immunosorbent assay - ELISA, indirect fluorescent antibody test - IFAT, immunochromatographic assay - IA), and clinical (hemogram, fever, weight loss) aspects were evaluated. During the acute phase of the disease, T. vivax was initially detected in Holstein/Gyr. Notably, the CPD animals restored their packed cell volume (PCV) values to the normal range 74 days after inoculations. In the chronic phase, two of the six CPD animals were positive by cPCR until D + 522 following immunosuppression with dexamethasone. Regarding serological aspects, the two CPD animals had positive tests until D + 532. The absence of T. vivax in blood during the chronic phase did not correspond to "self-cure". Holstein/Gyr animals exhibited fever on more evaluation days than CPD animals. Both breeds experienced weight loss, with Holstein/Gyr animals losing significantly more weight. On D + 25, the Holstein/Gyr group required treatment. During the 532 days, none of the CPD animals required treatment, even after being sensitized with dexamethasone. Animals from Group 3 tested negative for T. vivax throughout the experiment. This study demonstrated that CPD cattle fulfill the mentioned trypanotolerant criteria.
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