Current Advances in Detection and Treatment of Babesiosis

被引:228
作者
Mosqueda, J. [1 ]
Olvera-Ramirez, A. [1 ]
Aguilar-Tipacamu, G. [1 ]
Canto, G. J. [1 ]
机构
[1] Univ Autonoma Queretaro, Fac Ciencias Nat, Queretaro 76230, Mexico
关键词
Disease; ticks; prevention; cerebral babesiosis; blood smear; reverse line blot hybridization; indirect immunofluorescence; drug target; MEDIATED ISOTHERMAL AMPLIFICATION; LINKED-IMMUNOSORBENT-ASSAY; RHOPTRY-ASSOCIATED PROTEIN-1; REAL-TIME PCR; FLUORESCENT-ANTIBODY TEST; CHAIN-REACTION METHOD; WHITE-TAILED DEER; PLASMODIUM-FALCIPARUM; IN-VITRO; BOOPHILUS-MICROPLUS;
D O I
10.2174/092986712799828355
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Babesiosis is a disease with a world-wide distribution affecting many species of mammals principally cattle and man. The major impact occurs in the cattle industry where bovine babesiosis has had a huge economic effect due to loss of meat and beef production of infected animals and death. Nowadays to those costs there must be added the high cost of tick control, disease detection, prevention and treatment. In almost a century and a quarter since the first report of the disease, the truth is: there is no a safe and efficient vaccine available, there are limited chemotherapeutic choices and few low-cost, reliable and fast detection methods. Detection and treatment of babesiosis are important tools to control babesiosis. Microscopy detection methods are still the cheapest and fastest methods used to identify Babesia parasites although their sensitivity and specificity are limited. Newer immunological methods are being developed and they offer faster, more sensitive and more specific options to conventional methods, although the direct immunological diagnoses of parasite antigens in host tissues are still missing. Detection methods based on nucleic acid identification and their amplification are the most sensitive and reliable techniques available today; importantly, most of those methodologies were developed before the genomics and bioinformatics era, which leaves ample room for optimization. For years, babesiosis treatment has been based on the use of very few drugs like imidocarb or diminazene aceturate. Recently, several pharmacological compounds were developed and evaluated, offering new options to control the disease. With the complete sequence of the Babesia bovis genome and the B. bigemina genome project in progress, the post-genomic era brings a new light on the development of diagnosis methods and new chemotherapy targets. In this review, we will present the current advances in detection and treatment of babesiosis in cattle and other animals, with additional reference to several apicomplexan parasites.
引用
收藏
页码:1504 / 1518
页数:15
相关论文
共 195 条
[41]   Evaluation of an indirect fluorescence immunoassay for the detection of serum antibodies against Babesla divergens in humans [J].
Duh, D. ;
Jelovsek, M. ;
Avsic-Zupanc, T. .
PARASITOLOGY, 2007, 134 :179-185
[42]   The structure of lactate dehydrogenase from Plasmodium falciparum reveals a new target for anti-malarial design [J].
Dunn, CR ;
Banfield, MJ ;
Barker, JJ ;
Higham, CW ;
Moreton, KM ;
Turgut-Balik, D ;
Brady, RL ;
Holbrook, JJ .
NATURE STRUCTURAL BIOLOGY, 1996, 3 (11) :912-915
[43]   Molecular pharmacology and pharmacogenomics of artemisinin and its derivatives in cancer cells [J].
Efferth, T .
CURRENT DRUG TARGETS, 2006, 7 (04) :407-421
[44]  
Efferth T, 2003, INT J ONCOL, V23, P1231
[45]   Real-time PCR in clinical microbiology: Applications for a routine laboratory testing [J].
Espy, MJ ;
Uhl, JR ;
Sloan, LM ;
Buckwalter, SP ;
Jones, MF ;
Vetter, EA ;
Yao, JDC ;
Wengenack, NL ;
Rosenblatt, JE ;
Cockerill, FR ;
Smith, TF .
CLINICAL MICROBIOLOGY REVIEWS, 2006, 19 (01) :165-+
[46]   DETECTION OF BABESIA-BOVIS CARRIER CATTLE BY USING POLYMERASE CHAIN-REACTION AMPLIFICATION OF PARASITE DNA [J].
FAHRIMAL, Y ;
GOFF, WL ;
JASMER, DP .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (06) :1374-1379
[47]  
Fairclough R., 1962, CCTA PUBL, P81
[48]  
Fernando S D, 2004, Ceylon Med J, V49, P7
[49]   A plastid organelle as a drug target in apicomplexan parasites [J].
Fichera, ME ;
Roos, DS .
NATURE, 1997, 390 (6658) :407-409
[50]  
Figueroa J. V., 1994, Revista Latinoamericana de Microbiologia, V36, P47