Molecular characterization of Mycobacterium kansasii isolates in the state of Sao Paulo between 1995-1998

被引:15
作者
Chimara, E [1 ]
Giampaglia, CMS [1 ]
Martins, MC [1 ]
Telles, MAD [1 ]
Ueki, SYM [1 ]
Ferrazoli, L [1 ]
机构
[1] Inst Adolfo Lutz Registro, Setor Microbacterias, Secao Bacteriol, BR-01246902 Sao Paulo, Brazil
来源
MEMORIAS DO INSTITUTO OSWALDO CRUZ | 2004年 / 99卷 / 07期
关键词
Mycobacterium kansasii; nontuberculous mycobacteria; hsp65; restriction analysis;
D O I
10.1590/S0074-02762004000700013
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
Mycobacterium kansasii is the most common cause of pulmonary nontuberculous mycobacteria infection and classical identification of this pathogen needs a time consuming phenotypic tests. Polymerase chain reaction-restriction fragment lenght polymorphism analysis (PRA) of the gene enconding for the 65kDa heat shock (hsp65) protein offers an easy, rapid, and inexpensive procedure to identify and subtype M. kansasii isolates. In the present study, we performed a retrospective analysis of patients who had mycobacteria identified on the basis of phenotypic tests by means of a review of database at Mycobacteria Laboratory of the Instituto Adolfo Lutz in the period 1995-1998. A total of 9381 clinical isolates were analyzed of which 7777 (82.9%) were identified as M. tuberculosis complex and 1604 (17.1%) as nontuberculous mycobacteria. Of the 296 M. kausasii isolates, 189 (63.8%) isolates obtained from 119 patients were viable and were analyzed by PPA-hsp65. Hundred eight two (98.9%) were classified as M. kansasii type 1. Two isolates were classified as type II and III and five isolates were characterized as other Mycobacterium species. Clinical isolates of M. kansasii in the state of Sao Paulo was almost exclusively subtype of regardless of HIV status.
引用
收藏
页码:739 / 743
页数:5
相关论文
共 26 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]   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-+
[3]   CLINICAL-SIGNIFICANCE OF NONTUBERCULOUS MYCOBACTERIA ISOLATES IN A CANADIAN TERTIARY CARE CENTER [J].
CHOUDHRI, S ;
MANFREDA, J ;
WOLFE, J ;
PARKER, S ;
LONG, R .
CLINICAL INFECTIOUS DISEASES, 1995, 21 (01) :128-133
[4]   MYCOBACTERIA IN WATER [J].
COLLINS, CH ;
GRANGE, JM ;
YATES, MD .
JOURNAL OF APPLIED BACTERIOLOGY, 1984, 57 (02) :193-211
[5]  
da Silva C F, 2001, Rev Inst Med Trop Sao Paulo, V43, P25, DOI 10.1590/S0036-46652001000100005
[6]   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
[7]   Epidemiology of infection by nontuberculous mycobacteria [J].
Falkinham, JO .
CLINICAL MICROBIOLOGY REVIEWS, 1996, 9 (02) :177-+
[8]  
Garay JG, 2001, ARCH BRONCONEUMOL, V37, P27
[9]   IDENTIFICATION OF MYCOBACTERIUM-KANSASII BY DNA HYBRIDIZATION [J].
HUANG, ZH ;
ROSS, BC ;
DWYER, B .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (10) :2125-2129
[10]  
Joint Tuberculosis Committee BTS, 1999, THORAX, V2000, P210