Bovine trypanotolerance: A natural ability to prevent severe anaemia and haemophagocytic syndrome?

被引:106
作者
Naessens, J. [1 ]
机构
[1] Int Livestock Res Inst, Nairobi 00100, Kenya
基金
英国惠康基金;
关键词
trypanosomiasis; trypanotolerance; anemia; haemophagocytic syndrome; cattle; murine models; tumor necrosis factor alpha;
D O I
10.1016/j.ijpara.2006.02.012
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
Trypanotolerance is the capacity of certain West-African, taurine breeds of cattle to remain productive and gain weight after trypanosome infection. Laboratory studies, comparing Trypanosoma congolense infections in trypanotolerant N'Dama cattle (Bos taurus) and in more susceptible Boran cattle (Bos indicus), confirmed the field observations. Experiments using haemopoietic chimeric twins, composed of a tolerant and a susceptible co-twin, and T cell depletion studies suggested that trypanotolerance is composed of two independent traits. The first is a better capacity to control parasitaemia and is not mediated by haemopoietic cells, T lymphocytes or antibodies. The second is a better capacity to limit anaemia development and is mediated by haemopoietic cells, but not by T lymphocytes or antibodies. Weight gain was linked to the latter mechanism, implying that anaemia control is more important for survival and productivity than parasite control. Anemia is a marker for a more complex pathology which resembles human haemophagocytic syndrome: hepatosplenomegaly, pancytopenia and a large number of hyperactivated phagocytosing macrophages in bone marrow, liver and other tissues. Thus, mortality and morbidity in trypanosome-infected cattle are primarily due to self-inflicted damage by disproportionate immune and/or innate responses. These features of bovine trypanotolerance differ greatly from those in murine models. In mice, resistance is a matter of trypanosome control dependent on acquired immunity. However, a model of anaemia development can be established using C57BL/6J mice. As in cattle, the induction of anaemia was independent of T cells but its development differed with different trypanosome strains. Identification of the molecular pathways that lead to anaemia and haemophagocytosis should allow us to design new strategies to control disease. (c) 2006 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:521 / 528
页数:8
相关论文
共 78 条
[21]   Susceptibility of tumour necrosis factor-α genetically deficient mice to Trypanosoma congolense infection [J].
Iraqi, F ;
Sekikawa, K ;
Rowlands, J ;
Teale, A .
PARASITE IMMUNOLOGY, 2001, 23 (08) :445-451
[22]   Proinflammatory cytokines lowering erythropoietin production [J].
Jelkmann, W .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1998, 18 (08) :555-559
[23]   BRAIN AS A SOURCE OF RELAPSING TRYPANOSOMA-BRUCEI INFECTION IN MICE AFTER CHEMOTHERAPY [J].
JENNINGS, FW ;
WHITELAW, DD ;
HOLMES, PH ;
CHIZYUKA, HGB ;
URQUHART, GM .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1979, 9 (04) :381-384
[24]   CHEMOTHERAPY OF TRYPANOSOMA-BRUCEI INFECTION OF THE CENTRAL-NERVOUS-SYSTEM - THE USE OF A RAPID CHEMOTHERAPEUTIC REGIMEN AND THE DEVELOPMENT OF POSTTREATMENT ENCEPHALOPATHIES [J].
JENNINGS, FW ;
HUNTER, CA ;
KENNEDY, PGE ;
MURRAY, M .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1993, 87 (02) :224-226
[25]   The influence of energy intake on some blood biochemical parameters in Scottish Blackface sheep infected with Trypanosoma congolense [J].
Katunguka-Rwakishaya, E ;
Murray, M ;
Holmes, PH .
VETERINARY PARASITOLOGY, 1999, 84 (1-2) :1-11
[26]   PATHOPHYSIOLOGY OF OVINE TRYPANOSOMIASIS - FERROKINETICS AND ERYTHROCYTE SURVIVAL STUDIES [J].
KATUNGUKARWAKISHAYA, E ;
MURRAY, M ;
HOLMES, PH .
RESEARCH IN VETERINARY SCIENCE, 1992, 53 (01) :80-86
[27]   THE INFLUENCE OF ENERGY-INTAKE ON THE PATHOPHYSIOLOGY OF TRYPANOSOMA-CONGOLENSE INFECTION IN SCOTTISH BLACKFACE SHEEP [J].
KATUNGUKARWAKISHAYA, E ;
PARKINS, JJ ;
FISHWICK, G ;
MURRAY, M ;
HOLMES, PH .
VETERINARY PARASITOLOGY, 1995, 59 (3-4) :207-218
[28]   Genetic control of resistance to trypanosomiasis [J].
Kemp, SJ ;
Darvasi, A ;
Soller, M ;
Teale, AJ .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1996, 54 (1-4) :239-243
[29]   Genetic basis of trypanotolerance in cattle and mice [J].
Kemp, SJ ;
Teale, AJ .
PARASITOLOGY TODAY, 1998, 14 (11) :450-454
[30]   Localization of genes controlling resistance to trypanosomiasis in mice [J].
Kemp, SJ ;
Iraqi, F ;
Darvasi, A ;
Soller, M ;
Teale, AJ .
NATURE GENETICS, 1997, 16 (02) :194-196