Detection and identification of aquatic mycobacteria in formalin-fixed, paraffin-embedded fish tissues

被引:18
作者
Pourahmad, F. [1 ,2 ]
Thompson, K. D. [1 ]
Adams, A. [1 ]
Richards, R. H. [1 ]
机构
[1] Univ Stirling, Inst Aquaculture, Aquat Vaccine Unit, Stirling FK9 4LA, Scotland
[2] Ilam Univ, Sch Vet Med, Ilam, Iran
关键词
aquatic mycobacteria; detection; formalin-fixed; paraffin-embedded fish tissues hsp65 gene; POLYMERASE-CHAIN-REACTION; SP-NOV; GRANULOMATOUS INFLAMMATION; RAPID IDENTIFICATION; MOLECULAR-DETECTION; SPECIES LEVEL; RIBOSOMAL-RNA; PCR; TUBERCULOSIS; DNA;
D O I
10.1111/j.1365-2761.2009.01030.x
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
The isolation of mycobacteria from field samples is problematic, and isolation of the bacterium is sometimes not even attempted. The detection of mycobacteria through traditional histology using formalin-fixed, paraffin-embedded (FFPE) tissues is neither sensitive nor specific. However, detection of mycobacterial DNA from FFPE specimens, suspected of being infected with mammalian mycobacteriosis, is a routine clinical procedure. In the present study, a polymerase chain reaction (PCR)-based method was used to detect and identify mycobacteria in FFPE specimens sampled from fish suspected of being infected with fish mycobacteriosis. A total of 45 fish tissue samples, comprising of 12 tissue samples obtained from experimentally infected fish and the remainder from fish naturally infected with mycobacteria, were analysed using a PCR protocol which amplifies a fragment of the mycobacterial 65 kDa heat-shock protein (hsp65) gene. PCR-restriction enzyme analysis and/or sequencing were employed to further analyse the PCR amplicons. The PCR results were compared with those obtained by histology and culture. Mycobacterial DNA was detected in 34 of the 45 samples examined, of which 16 samples (47%) showed granulomatous reactions on histological examination. Using histology as the gold standard, no false-negative PCR results were obtained. Also, considering the presence or absence of granulomas as a diagnostic criterion, the sensitivity and specificity of PCR in 42 of the FFPE tissues were 16/16 (100%) and 8/26 (similar to 30.8%), respectively. Corresponding microbiological cultures were available for 15 cases, of which 13 were pure Mycobacterium cultures. Of these, 13 were PCR positive (100% sensitivity and 50% specificity). The PCR-based methods used here proved sensitive, specific and rapid for the detection of mycobacteria in routinely processed paraffin wax-embedded and formalin-fixed histological samples, and the results of the study suggest that this method has potential use in retrospective epidemiological studies.
引用
收藏
页码:409 / 419
页数:11
相关论文
共 44 条
[1]   Improved diagnosis of mycobacterial infections mi formalin-fixed and paraffin-embedded sections with nested polymerase chain reaction [J].
Azov, AG ;
Koch, J ;
Hamilton-Dutoit, SJ .
APMIS, 2005, 113 (09) :586-593
[2]  
Bascunana CR, 1996, J CLIN MICROBIOL, V34, P2351
[3]   Distribution of mycobacteria in clinically healthy ornamental fish and their aquarium environment [J].
Beran, V. ;
Matlova, L. ;
Dvorska, L. ;
Svastova, P. ;
Pavlik, I. .
JOURNAL OF FISH DISEASES, 2006, 29 (07) :383-393
[4]   16S ribosomal RNA sequence-based identification of veterinary clinical bacteria [J].
Cai, H ;
Archambault, M ;
Prescott, JF .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2003, 15 (05) :465-469
[5]  
CHIANG IP, 2005, MID TAIWAN J MED, V10, P25
[6]   Distribution of environmental mycobacteria in Karonga District, northern Malawi [J].
Chilima, BZ ;
Clark, IM ;
Floyd, S ;
Fine, PEM ;
Hirsch, PR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2006, 72 (04) :2343-2350
[7]   Identification of Mycobacterium marinum in sea-urchin granulomas [J].
De la Torre, C ;
Vega, A ;
Carracedo, A ;
Toribio, J .
BRITISH JOURNAL OF DERMATOLOGY, 2001, 145 (01) :114-116
[8]   Rapid identification of mycobacteria to species level by PCR-restriction fragment length polymorphism analysis of the hsp65 gene and proposition of an algorithm to differentiate 34 mycobacterial species [J].
Devallois, A ;
Goh, KS ;
Rastogi, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (11) :2969-2973
[9]   Potential role for fish in transmission of Mycobactetium ulcerans disease (Buruli ulcer):: an environmental study [J].
Eddyani, M ;
Ofori-Adjei, D ;
Teugels, G ;
De Weirdt, D ;
Boakye, D ;
Meyers, WM ;
Portaels, F .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (09) :5679-5681
[10]   Detection of Mycobacterium avium subspecies paratuberculosis in free-ranging bison (Bison bison) by PCR [J].
Ellingson, JLE ;
Stabel, JR ;
Radcliff, RP ;
Whitlock, RH ;
Miller, JM .
MOLECULAR AND CELLULAR PROBES, 2005, 19 (03) :219-225