Detection of genetic diversity of Anaplasma marginale isolates in Minas Gerais, Brazil

被引:35
作者
Pohl, Anna Elisabeth [1 ]
Cabezas-Cruz, Alejandro [2 ]
Barbosa Ribeiro, Mucio Flavio [3 ]
Goncalves da Silveira, Julia Angelica [3 ]
Silaghi, Cornelia
Pfister, Kurt [1 ]
Friche Passos, Lygia Maria [1 ,4 ]
机构
[1] LMU, Inst Comparat Trop Med & Parasitol, D-80752 Munich, Germany
[2] Univ South Bohemia, Fac Sci, Parasitol Inst IP, Biol Ctr,Acad Sci Czech Republ,Vvi, Ceske Budejovice 37005, Czech Republic
[3] Univ Fed Minas Gerais, ICB, Dept Parasitol, Belo Horizonte, MG, Brazil
[4] Univ Fed Minas Gerais, Escola Vet, INCT Informacao Genet Sanit Pecuaria Brasileria, Dept Med Vet Prevent, Belo Horizonte, MG, Brazil
来源
REVISTA BRASILEIRA DE PARASITOLOGIA VETERINARIA | 2013年 / 22卷 / 01期
关键词
Anaplasma marginale; MSP1a; DNA sequencing; microsatellites; tandem repeats; Brazil; MULTIPLE SEQUENCE ALIGNMENT; BOVINE ANAPLASMOSIS; TRANSMISSION; LIKELIHOOD; ALGORITHM; SELECTION; ACCURATE; CATTLE; DNA;
D O I
10.1590/S1984-29612013000100024
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
Bovine anaplasmosis, caused by the tick-borne rickettsia Anaplasma marginale, is endemic in tropical and subtropical regions of the world and results in economic losses in the cattle industry. Major surface proteins (MSPs) have been used as markers for the genetic characterization of A. marginale strains and demonstrate that many isolates may occur in a given geographic area. However, in Brazil, little is known about the genetic diversity of A. marginale isolates within individual herds. This study was designed to examine the genetic variation among A. marginale infecting calves in a farm in the south of Minas Gerais State, Brazil. Blood samples collected from 100 calves were used to prepare Giemsa-stained smears that were microscopically examined for the presence of A. marginale. From each blood sample, DNA was extracted and analyzed by a polymerase chain reaction (PCR), followed by sequencing to determine diversity among the isolates. Examination of blood smears showed that 48% of the calves were infected with A. marginale, while the real-time PCR detected 70.2% positivity. Congenital infections were found in four calves. The microsatellite and tandem repeat analyses showed high genetic diversity among the isolates.
引用
收藏
页码:129 / 135
页数:7
相关论文
共 24 条
[1]   Approximate likelihood-ratio test for branches: A fast, accurate, and powerful alternative [J].
Anisimova, Maria ;
Gascuel, Olivier .
SYSTEMATIC BIOLOGY, 2006, 55 (04) :539-552
[2]   A Review of Bovine Anaplasmosis [J].
Aubry, P. ;
Geale, D. W. .
TRANSBOUNDARY AND EMERGING DISEASES, 2011, 58 (01) :1-30
[3]   Detection and quantification of Anaplasma marginale DNA in blood samples of cattle by real-time PCR [J].
Carelli, G. ;
Decaro, N. ;
Lorusso, A. ;
Elia, G. ;
Lorusso, E. ;
Mari, V. ;
Ceci, L. ;
Buonavoglia, C. .
VETERINARY MICROBIOLOGY, 2007, 124 (1-2) :107-114
[4]   Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis [J].
Castresana, J .
MOLECULAR BIOLOGY AND EVOLUTION, 2000, 17 (04) :540-552
[5]   TreeDyn:: towards dynamic graphics and annotations for analyses of trees [J].
Chevenet, Francois ;
Brun, Christine ;
Banuls, Anne-Laure ;
Jacq, Bernard ;
Christen, Richard .
BMC BIOINFORMATICS, 2006, 7 (1)
[6]   Anaplasma marginale msp1α genotypes evolved under positive selection pressure but are not markers for geographic isolates [J].
de la Fuente, J ;
Van Den Bussche, RA ;
Prado, TM ;
Kocan, KM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (04) :1609-1616
[7]   Characterization of the functional domain of major surface protein 1a involved in adhesion of the rickettsia Anaplasma marginale to host cells [J].
de la Fuente, J ;
Garcia-Garcia, JC ;
Blouin, EF ;
Kocan, KM .
VETERINARY MICROBIOLOGY, 2003, 91 (2-3) :265-283
[8]   Phylogeography of New World isolates of Anaplasma marginale based on major surface protein sequences [J].
de la Fuente, J ;
Van Den Bussche, RA ;
Garcia-Garcia, JC ;
Rodríguez, SD ;
García, MA ;
Guglielmone, AA ;
Mangold, AJ ;
Passos, LMF ;
Ribeiro, MFB ;
Blouin, EF ;
Kocan, KM .
VETERINARY MICROBIOLOGY, 2002, 88 (03) :275-285
[9]  
de la Fuente J, 2007, VET MICROBIOL, V119, P375, DOI [10.1016/j.vetmic.2006.09.011, 10.1016/j.vetmic.2006.09.015]
[10]  
de la Fuente Jose, 2005, Anim Health Res Rev, V6, P75, DOI 10.1079/AHR2005104