Identification of 54 mycobacterial species by PCR-restriction fragment length polymorphism analysis of the hsp65 gene

被引:124
作者
Brunello, F
Ligozzi, M
Cristelli, E
Bonora, S
Tortoli, E
Fontana, R
机构
[1] Univ Verona, Dipartimento Patol, Sez Microbiol, I-37100 Verona, Italy
[2] Azienda Ospedaliera Verona, Microbiol Serv, I-37100 Verona, Italy
[3] Univ Turin, Clin Malattie Infett, Turin, Italy
[4] Osped Careggi Firenze, Microbiol Serv, Florence, Italy
[5] Ctr Riferimento Nazl Micobatteri, Florence, Italy
关键词
D O I
10.1128/JCM.39.8.2799-2806.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A total of 121 reference and clinical strains of both slowly and rapidly growing mycobacteria belonging to 54 species were studied for restriction fragment length polymorphism of a PCR-amplified 439-bp segment of the gene encoding the 65-kDa heat shock protein. Restriction digests were separated by 10% polyacrylamide gel electrophoresis (PAGE). By including a size standard in each sample, the restriction fragment profile was calculated using a computer-aided comparison program. An algorithm describing these 54 species (including 22 species not previously described) is proposed. We found that this assay based on 10% PAGE provided a more precise estimate than that based on agarose gel electrophoresis of the real size of restriction fragments as deduced from the sequence analysis and allowed identification of mycobacteria whose PCR-restriction fragment length polymorphism analysis patterns were unequivocally identified by fragments shorter than 60 bp.
引用
收藏
页码:2799 / 2806
页数:8
相关论文
共 31 条
[1]   Heterogeneity and clonality among isolates of Mycobacterium kansasii: Implications for epidemiological and pathogenicity studies [J].
Alcaide, F ;
Richter, I ;
Bernasconi, C ;
Springer, B ;
Hagenau, C ;
SchulzeRobbecke, R ;
Tortoli, E ;
Martin, R ;
Bottger, EC ;
Telenti, A .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (08) :1959-1964
[2]  
Alcaide F, 2000, J CLIN MICROBIOL, V38, P398
[3]   Molecular technique for rapid identification of mycobacteria [J].
AvanissAghajani, E ;
Jones, K ;
Holtzman, A ;
Aronson, T ;
Glover, N ;
Boian, M ;
Froman, S ;
Brunk, CF .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (01) :98-102
[4]  
Bahrmand AR, 1998, SCAND J INFECT DIS, V30, P477, DOI 10.1080/00365549850161476
[5]   Incidence and clinical implications of isolation of Mycobacterium kansasii:: Results of a 5-year, population-based study [J].
Bloch, KC ;
Zwerling, L ;
Pletcher, MJ ;
Hahn, JA ;
Gerberding, JL ;
Ostroff, SM ;
Vugia, DJ ;
Reingold, AL .
ANNALS OF INTERNAL MEDICINE, 1998, 129 (09) :698-+
[6]   Comparison of the MB/BacT and BACTEC 460 TB systems for recovery of mycobacteria from various clinical specimens [J].
Brunello, F ;
Favari, F ;
Fontana, R .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (04) :1206-1209
[7]   Comparative evaluation of PCR and commercial DNA probes for detection and identification to species level of Mycobacterium avium and Mycobacterium intracellulare [J].
Devallois, A ;
Picardeau, M ;
Goh, KS ;
Sola, C ;
Vincent, V ;
Rastogi, N .
JOURNAL OF CLINICAL MICROBIOLOGY, 1996, 34 (11) :2756-2759
[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]   DETECTION AND IDENTIFICATION OF MYCOBACTERIA BY AMPLIFICATION OF MYCOBACTERIAL DNA [J].
HANCE, AJ ;
GRANDCHAMP, B ;
LEVYFREBAULT, V ;
LECOSSIER, D ;
RAUZIER, J ;
BOCART, D ;
GICQUEL, B .
MOLECULAR MICROBIOLOGY, 1989, 3 (07) :843-849
[10]   Identification of Mycobacterium species by PCR-restriction fragment length polymorphism analyses using fluorescence capillary electrophoresis [J].
Hernandez, SM ;
Morlock, GP ;
Butler, WR ;
Crawford, JT ;
Cooksey, RC .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (11) :3688-3692