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

IF 1.4 Q3 PARASITOLOGY
Débora Ribeiro de Mendonça , Luiz Fellipe Monteiro Couto , Luana Hernandez Pureza , Danieli Brolo Martins , Vando Edésio Soares , Lorena Lopes Ferreira , Maria Clorinda Soares Fioravanti , Thiago Souza Azeredo Bastos , Paulo Henrique Jorge da Cunha , Welber Daniel Zanetti Lopes
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引用次数: 0

Abstract

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 Pé-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.

拉丁美洲首个可能耐受锥虫病的牛种记录:寄生虫学、血清学和临床方面的问题
体内锥虫感染是非洲的地方病,在那里会引发锥虫病,而当地的一些金牛品种对锥虫病有耐受力,因此被命名为耐锥虫病金牛。在拉丁美洲,1919 年传入了 T. vivax,从那时起,这种病就开始定期爆发。本研究评估了对多种寄生虫病和传染病有抵抗力的南美金牛品种(Curraleiro Pé-Duro-CPD)是否符合耐锥虫病标准(控制寄生虫增殖、预防贫血、无需治疗即可存活并保持生产力)。共分三组,每组六只动物(第 1 组:CPD 感染组;第 2 组:荷斯坦/Gyr 感染组;第 3 组:荷斯坦/Gyr 未感染组,阴性对照组)。第 1 组和第 2 组在第 0 天感染间日疟原虫,直到第 532 天进行评估。在整个实验期间,对寄生虫学(Woo 和 Brener)、分子(cPCR)、血清学(酶联免疫吸附试验 - ELISA、间接荧光抗体检测 - IFAT、免疫层析检测 - IA)和临床(血象图、发烧、体重减轻)进行了评估。在疾病的急性期,最初在荷斯坦/吉尔牛中发现了间日疟原虫。值得注意的是,接种后 74 天,CPD 动物的充盈细胞体积 (PCV) 值恢复到正常范围。在慢性期,六只 CPD 动物中有两只在使用地塞米松进行免疫抑制后,cPCR 阳性一直持续到 D + 522。在血清学方面,两只 CPD 动物的检测结果呈阳性,直至 D + 532。慢性期血液中未检出间日疟原虫并不意味着 "自愈"。荷斯坦/吉尔动物比 CPD 动物在更多的评估日表现出发热。两个品种的动物都出现了体重减轻,其中荷斯坦/吉尔动物的体重减轻幅度更大。在 D + 25 天,荷斯坦/吉尔组需要进行治疗。在 532 天内,CPD 动物无一需要治疗,即使在使用地塞米松增敏后也是如此。在整个实验过程中,第 3 组动物的间日疟原虫检测结果均为阴性。这项研究表明,CPD 牛符合上述锥虫病耐受标准。
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来源期刊
CiteScore
2.90
自引率
7.10%
发文量
126
审稿时长
97 days
期刊介绍: Veterinary Parasitology: Regional Studies and Reports focuses on aspects of veterinary parasitology that are of regional concern, which is especially important in this era of climate change and the rapid and often unconstrained travel of people and animals. Relative to regions, this journal will accept papers of the highest quality dealing with all aspects of disease prevention, pathology, treatment, epidemiology, and control of parasites within the field of veterinary medicine. Also, case reports will be considered as they add to information related to local disease and its control; such papers must be concise and represent appropriate medical intervention. Papers on veterinary parasitology from wildlife species are acceptable, but only if they relate to the practice of veterinary medicine. Studies on vector-borne bacterial and viral agents are suitable, but only if the paper deals with vector transmission of these organisms to domesticated animals. Studies dealing with parasite control by means of natural products, both in vivo and in vitro, are more suited for one of the many journals that now specialize in papers of this type. However, due to the regional nature of much of this research, submissions may be considered based upon a case being made by the author(s) to the Editor. Circumstances relating to animal experimentation must meet the International Guiding Principles for Biomedical Research Involving Animals as issued by the Council for International Organizations of Medical Sciences (obtainable from: Executive Secretary C.I.O.M.S., c/o W.H.O., Via Appia, CH-1211 Geneva 27, Switzerland).
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