Evaluation of the abbott LCx Mycobacterium tuberculosis assay for direct detection of Mycobacterium bovis in bovine tissue samples

被引:0
作者
Valente, C
Cuteri, V
Ausili, E
Piersimoni, C
机构
[1] Univ Perugia, Sch Vet Med, I-06100 Perugia, Italy
[2] Gen Hosp Umberto 1 Torrette, Dept Clin Microbiol, Ancona, Italy
[3] Univ Camerino, Dept Vet Sci, I-62032 Camerino, Italy
关键词
cattle; diagnosis; DNA amplification; ligase chain reaction; lymph node; Mycobacterium bovis; tuberculosis;
D O I
10.1023/A:1013349504066
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The commercial LCx amplification assay, usually employed to detect the Mycobacterium tuberculosis complex in respiratory specimens, was evaluated by comparing the results it gave with those obtained using Lowenstein-Jensen solid medium and pathological findings on 55 lymph nodes from cattle with positive and 10 lymph nodes from cattle with negative skin tests for tuberculosis. Fifty-three cultures (51 and 2, respectively) were positive for M. bovis, while the results for the LCx assay and the histological method were positive in 48 (45, 3) and 24 (20, 4) samples, respectively. None of the samples from cattle from certified tuberculosis-free herds were positive by any of the procedures. The results obtained with the LCx assay, compared with the culture procedure, regarded as the gold standard among the diagnostic techniques, gave a specificity of 91.6% and sensitivity of 90.5%. Although the sensitivity of LCx was suboptimal, DNA of M. bovis was detected in 81.8% of the skin test-positive animals. Amplification techniques could provide a rapid and reasonably reliable tool for detecting bovine tuberculosis.
引用
收藏
页码:21 / 27
页数:7
相关论文
共 18 条
[1]   Direct detection of Mycobacterium tuberculosis complex and M-avium complex in tissue specimens from cattle through identification of specific rRNA sequences [J].
Bollo, E ;
Guarda, F ;
Capucchio, MT ;
Galietti, F .
JOURNAL OF VETERINARY MEDICINE SERIES B-INFECTIOUS DISEASES AND VETERINARY PUBLIC HEALTH, 1998, 45 (07) :395-400
[2]  
Cavirani S, 1999, MICROBIOLOGICA, V22, P343
[3]  
CHEESEMAN CL, 1981, J ZOOL, V194, P284, DOI 10.1111/j.1469-7998.1981.tb05780.x
[4]   TUBERCULOSIS IN DEER - A REVIEW [J].
CLIFTONHADLEY, RS ;
WILESMITH, JW .
VETERINARY RECORD, 1991, 129 (01) :5-12
[5]   Performance of the single intradermal comparative tuberculin test in identifying cattle with tuberculous lesions in Irish herds [J].
Costello, E ;
Egan, JWA ;
Quigley, FC ;
OReilly, PF .
VETERINARY RECORD, 1997, 141 (09) :222-224
[6]  
Fadda G, 1998, MICROBIOLOGICA, V21, P97
[7]   SENSITIVITY AND SPECIFICITY OF VARIOUS TUBERCULIN TESTS USING BOVINE PPD AND OTHER TUBERCULINS [J].
FRANCIS, J ;
SEILER, RJ ;
WILKIE, IW ;
OBOYLE, D ;
LUMSDEN, MJ ;
FROST, AJ .
VETERINARY RECORD, 1978, 103 (19) :420-425
[8]   Rapid diagnosis of extrapulmonary tuberculosis by ligase chain reaction amplification [J].
Gamboa, F ;
Dominguez, J ;
Padilla, E ;
Manterola, JM ;
Gazapo, E ;
Lonca, J ;
Matas, L ;
Hernandez, A ;
Cardona, PJ ;
Ausina, V .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (05) :1324-1329
[9]  
LIEBANA E, 1995, J CLIN MICROBIOL, V33, P33
[10]   Multicenter evaluation of the Abbott LCx Mycobacterium tuberculosis ligase chain reaction assay [J].
Lumb, R ;
Davies, K ;
Dawson, D ;
Gibb, R ;
Gottlieb, T ;
Kershaw, C ;
Kociuba, K ;
Nimmo, G ;
Sangster, N ;
Worthington, M ;
Bastian, I .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (10) :3102-3107