hsp65 sequencing for identification of rapidly growing mycobacteria

Abstract

Partial sequencing of the hsp65 gene was used for the identification of rapidly growing mycobacteria (RGM). A 441-bp fragment (A. Telenti, F. Marchesi, M. Balz, F. Bally, E. Böttger, and T. Bodmer, J. Clin. Microbiol. 31:175-178, 1993) was amplified and sequenced by an automated fluorescence-based method involving capillary electrophoresis. Type strains of 10 RGM species were first studied. Each species had a unique nucleotide sequence, distinguishing it clearly from the other species. A panel of strains from the four main RGM species responsible for human infections, Mycobacterium abscessus, Mycobacterium chelonae, Mycobacterium fortuitum, and Mycobacterium peregrinum, was also studied. There were few sequence differences within each of these species (<2% of bases were different from the type strain sequence), and they had no effect on species assignment. hsp65 sequencing unambiguously differentiated M. chelonae and M. abscessus, two species difficult to identify by classical methods and 16S rRNA gene sequencing. The devised procedure is a rapid and reliable tool for the identification of RGM species.

FIG. 1

Alignment of partial hsp65 sequences from RGM type strains. M. tuberculosis was used as a reference; nucleotides differing from those of the M. tuberculosis sequence are indicated; dots indicate identity. The first nucleotide shown corresponds to position 416 of the published sequence from M. tuberculosis (21).

FIG. 2

Unrooted phylogenetic tree based upon hsp65 sequences from RGM type strains. The tree was constructed by using the neighbor-joining method. The bar indicates 1% estimated sequence divergence.