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Previous Article | Next Article 
Journal of Clinical Microbiology, January 2000, p. 301-308, Vol. 38, No. 1
Marine Biotechnology Institute, Kamaishi
Laboratories, 3-75-1 Heita, Kamaishi, Iwate
026-0001,1 and Department of
Microbiology, Gifu University School of Medicine, Gifu, Gifu
500-8705,2 Japan
Received 27 May 1999/Returned for modification 18 August
1999/Accepted 4 October 1999
The conventional methods for identifying mycobacterial species are
based on their phenotypic characterization. Since some problematic
species are slow growers, their taxonomy takes several weeks or months
to identify. The ribosomal DNA (rDNA) sequence-based identification
strategy has been adopted to solve this problem. More recently, the
gyrB sequences have been shown to be useful phylogenetic
markers for the identification of species. We determined the
gyrB sequences of 43 slowly growing strains belonging to 15 species in the genus Mycobacterium. The frequencies of base
substitutions in the gyrB sequences were comparable to
those in the 16S-23S rDNA internal transcribed spacer (ITS) sequences.
The ITS sequences of four species belonging to the M. tuberculosis complex (M. tuberculosis, M. bovis, M. africanum, and M. microti) were
100% identical, while four synonymous substitutions were found in the
gyrB sequences of these strains. Based on the differences
found in the gyrB sequences, we developed PCR and
PCR-restriction fragment length polymorphism methods to discriminate
these species.
The increase in the incidence of
infection by mycobacteria in humans, especially among immunocompromised
patients, is a matter of serious concern to the public. In order to
control this infection, rapid identification of the carriers of
mycobacteria is a high priority. Intensive research efforts were made
to develop rapid methods for identifying mycobacteria. Numerical
taxonomic matrices and 16S ribosomal DNA (rDNA)-based phylogenetic
analyses have provided a great deal of information on the systematics
of mycobacteria (19, 24, 37). The 16S rDNA-based methods are
currently widely accepted as rapid and accurate means for identifying
mycobacteria (14, 15, 28). However, it was found that the
distinctions between Mycobacterium kansasii and M. gastri, between M. malmoense and M. szulgai,
between M. marinum and M. ulcerans, and between the members of the M. tuberculosis complex are difficult to
make based on their 16S rDNA sequences since they are almost identical between these strains. To solve this problem, the sequences of the
16S-23S rDNA internal transcribed spacer (ITS) have been used to
distinguish between M. kansasii and M. gastri
(20). However, the ITS sequences are identical among the
M. tuberculosis complex strains.
The M. tuberculosis complex consists of four closely related
groups, M. tuberculosis, M. bovis, M. africanum, and M. microti, and they may be considered
to be subspecies of M. tuberculosis (37). Their
close relatedness has been demonstrated by DNA-DNA hybridization
(1), isozyme analysis (5), and electrokaryotyping (5). However, their host range and pathogenicity are quite different. The host of M. tuberculosis and M. africanum is limited to humans (37), while M. bovis causes disease in a wide range of wild and domestic mammals,
as well as in humans (18). M. microti has
recently been reported to infect not only voles but also humans
(32).
Several efforts have been made to differentiate slowly growing
mycobacterial species by using protein-encoding genes such as the
32-kDa protein gene (22), dnaJ (26, 27,
34), hsp 65 (17, 25), the superoxide
dismutase gene (21, 44), recA (31),
and rpoV (3). However, DNA sequence analyses of
these genes revealed them to be invariant among the members of the
M. tuberculosis complex.
Yamamoto and Harayama (40) have proposed that
gyrB could be a suitable phylogenetic marker for the
identification and classification of bacteria (10, 41, 42).
They have shown that the divergence of gyrB sequences
reflected the taxonomical relationships in the genera
Acinetobacter (42) and Pseudomonas
(43). They have also shown that the average base
substitution rate of 16S rDNA was 1% per 50 million years, while that
of the gyrB genes at synonymous sites was 0.7 to 0.8% per
one million years (41). The gyrB analyses of other bacterial genera have also resolved closely related strains (33, 35, 36, 39).
In this report, we analyzed the gyrB sequences of type
strains and clinical isolates of slowly growing mycobacteria, including the M. tuberculosis complex, M. kansasii,
M. gastri, M. avium, M. intracellulare, M. malmoense, and M. simiae.
In parallel, we analyzed the ITS sequences of these strains and
compared the results with those of the gyrB analysis.
Furthermore, we developed PCR-based methods to differentiate four
species of the M. tuberculosis complex.
Strains and cultivation.
The strains used in
this study are shown in Table 1. They
were cultivated by using Ogawa's medium (Nissui Pharmaceutical Co.).
0095-1137/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Differentiation of Phylogenetically Related Slowly
Growing Mycobacteria by Their gyrB Sequences
ABSTRACT
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References
INTRODUCTION
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References
TABLE 1.
Source of DNA samples and accession numbers of
gyrB sequences
Determination of gyrB gene sequences.
The
protocol for determining the gyrB sequences was almost the
same as that described by Yamamoto and Harayama except for the PCR
primers (40). The primers used here are listed in Table 2, the location of each primer sequence
being indicated by the numbering system for the M. tuberculosis
gyrB sequence. A 1.2-kb gyrB segment was amplified by
PCR by using the universal primers UP1TL and UP2rTL. To determine the
nucleotide sequence of both strands of the gyrB segment,
shorter fragments were amplified by using the PCR-amplified 1.2-kb
gyrB segment as a template and two pairs of primers, either
UP1EM13r plus QTK-21 or GGTH-r plus UP2r-21. The amplification reaction
was subjected to 35 cycles with a denaturation step at 95°C for 1 min, an annealing step at 63°C for 1 min, and an extension step at
72°C for 2 min. Sequences were determined by using the universal
primers for the M13 phage vector.
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Determination of ITS sequences. The ITS sequences were determined by using the primers Ec16S.1390p (5'-TTGTACACACCGCCCGTC-3') and Mb23S.44n (5'-TCTCGATGCCAAGGCATCCACC-3') (20). The amplification reaction was subjected to 35 cycles with a denaturation step at 95°C for 1 min, an annealing step at 63°C for 1 min, and an extension step at 72°C for 1 min. The amplified DNA was purified, and its sequence was determined by using Ec16S.1390p and Mb23S.44n as sequence primers.
ETR typing. Exact tandem repeat (ETR) typing was performed by using the combination of primers designated ETR-A and heat-treated crude lysates as DNA templates (7). The amplification reaction was subjected to 35 cycles with a denaturation step at 95°C for 1 min, an annealing step at 60°C for 1 min, and an extension step at 72°C for 2 min. Amplified fragment was analyzed by 1.5% agarose gel electrophoresis for typing.
Analysis of sequence data. The gyrB sequences were aligned by using CLUSTAL W 1.7 (29), and the alignment was manually corrected. Phylogenetic analyses were performed by the PHYLIP version 3.5c package (6). Distance matrices based on Kimura's two-parameter model (12) were produced by using the DNADIST program, and a neighbor-joining tree was constructed by using the NEIGHBOR program. The resulting trees were depicted by using the TreeView version 1.5 package (16). The stability of the grouping was assessed by bootstrapping with the SEQBOOT, DNADIST, NEIGHBOR, and CONSENSE programs. A total of 1,000 bootstrapped trees were generated. Pairwise distances of the gyrB or ITS sequences were calculated by using the MEGA version 1.0 package (13).
gyrB-based species-specific PCR for the M. tuberculosis complex. The gyrB sequences of four type strains belonging to the M. tuberculosis complex were aligned, and the four sites at which base substitutions occurred were found. Species-specific primers whose 3' ends were at the base substitution sites were designed and named 675-T, 756-G, 756-A, 1410-G, 1410-A, 1450-C, and 1450-A (Table 2). The PCR reactions were performed in a final volume of 20 µl containing 1 µl of a boiled bacterial suspension, a reaction buffer (GeneAmp Kit; Perkin-Elmer), 1.25 U of AmpliTaq Gold DNA polymerase, a 0.1 mM concentration of each deoxynucleoside triphosphate, and 100 pmol of each primer. The reaction was subjected to 35 cycles of amplification, with a denaturation step at 95°C for 1 min and an annealing-extension step at 72°C for 1.5 min, by using a Progene thermal cycler (Techne). The amplified fragments were analyzed by 1.5% agarose gel electrophoresis.
gyrB-based species-specific PCR for M. kansasii and M. gastri. The gyrB sequences of the type strains of M. kansasii and M. gastri were aligned with those of other mycobacterial and related species. The sequences specific to M. kansasii and M. gastri were then found. Species-specific primers whose 3' ends corresponded to the species-specific sequences were designed and named KG632f, MK962r, and MG962r (Table 2). The PCR reactions were performed in a final volume of 20 µl containing 1 µl of a boiled bacterial suspension, a reaction buffer (GeneAmp Kit), 1.25 U of AmpliTaq Gold DNA polymerase, a 0.1 mM concentration of each deoxyribonucleoside triphosphate, and 100 pmol of each primer. The reaction was subjected to 30 cycles of amplification, with a denaturation step at 95°C for 1 min and an annealing-extension step at 68°C for 1.5 min, by using a Progene thermal cycler (Techne). The amplified fragments were analyzed by 1.5% agarose gel electrophoresis.
PCR-restriction fragment length polymorphism (RFLP) analysis. The mycobacterial GyrB amino acid sequences were aligned, and two regions specific to the M. tuberculosis complex were found. Primers, which were designed from the specific amino acid sequences were named MTUBf and MTUBr (Table 2) and used for PCR. The PCR reaction was performed under the same conditions as those for species-specific PCR already described. The amplified fragments were digested with RsaI and TaqI, the digested fragments being analyzed by 2.0% agarose gel electrophoresis.
DNA-DNA hybridization. The levels of DNA-DNA relatedness were determined fluorometrically by the method of Ezaki et al. (4) by using biotinylated DNA.
Nucleotide sequence accession numbers. The gyrB and ITS sequences determined in this study have been deposited in DDBJ (DNA DataBank of Japan) under the accession numbers shown in Table 1.
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RESULTS AND DISCUSSION |
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Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References
|
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Phylogenetic analysis of slowly growing mycobacteria based on their gyrB sequences. Primers UP1TL and UP2rTL were used to amplify ~1.2-kb gyrB fragments by PCR from 15 mycobacterial species, and their nucleotide sequences were determined. The sizes of the amplified gyrB fragments were 1,257 bp for the M. tuberculosis complex, M. kansasii, and M. gastri, while those for the other species were longer by 6 bp. The alignment of the translated sequences showed that two residues were inserted in the N-terminal region: the amino acid sequences of the N terminus were Ser-Asp-(Ser or Ala)-Tyr-Ala-Ile-Ser for M. kansasii, M. gastri, and the M. tuberculosis complex, whereas they were Gly-Glu-Asn-Ser-Gly-Tyr-(Asn or Thr)-Val-Ser for the other species. The overall amino acid sequence identities ranged from 82 to 99%. The pairs showing more than 90% identity were M. kansasii and M. gastri (94%), M. avium and M. intracellulare (91%), and four species of the M. tuberculosis complex (99%). The other pairs showed <90% identity. The unrooted phylogenetic tree (Fig. 1) showed that the 15 mycobacterial species were well resolved by their gyrB sequences. Especially, branches of medically important species, such as M. kansasii, M. gastri, M. avium, M. intracellulare, and M. tuberculosis complex, were supported by high bootstrap values. The results indicated that the gyrB sequences would be useful for differentiation of those species.
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Identification of M. kansasii and M. gastri by gyrB-targeted species-specific PCR. The gyrB sequences of the type strains of M. gastri and M. kansasii were 94.7% identical (1,191 of 1,257 bp). All except five substitutions were synonymous. The gyrB sequences of eight clinical isolates were determined to identify intraspecies variations in the gyrB sequences. The taxonomic identification of these isolates was done by DNA-DNA hybridization experiments: six of them were identified to be M. kansasii, and the remaining two were determined to be M. gastri. The gyrB sequences of these isolates were 100% identical to those of the type strains. Two stretches of DNA were found to be specific to M. kansasii and/or M. gastri when their gyrB sequences were aligned with those of 350 strains of high G+C gram-positive bacteria (H. Kasai and S. Harayama, unpublished data). Their locations corresponded to positions 613 to 632 and positions 962 to 981 of the M. tuberculosis gyrB sequence (GenBank accession number L27512). A set of primers adapted to these two specific sequences was designed. The forward primer was complementary to both the M. kansasii and M. gastri sequences, while two types of reverse primers, one specific to M. kansasii and the other specific to M. gastri, were prepared. As shown in Fig. 2, M. kansasii and M. gastri could be distinguished by PCR with these primer sets.
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gyrB sequences of strains in the M. tuberculosis complex. We determined the gyrB sequences of the type strains of M. tuberculosis, M. microti, M. africanum, and M. bovis. The obtained sequences were compared with each other, and we found substitutions at four different sites (Fig. 3A). At position 675, the gyrB sequence of M. microti was T, and the gyrB sequences of the other strains were C. At position 756, the gyrB sequence of M. bovis was A, and the gyrB sequences of the other strains were G. At position 1410, the gyrB sequence of M. bovis was T, and the gyrB sequences of the other strains were C. At position 1450, the gyrB sequence of M. tuberculosis was G, and the gyrB sequences of the other strains were T. All the substitutions were synonymous, three being transitions and one being a transversion. These substitutions are unlikely to have developed under the selective pressure of therapeutic drug treatment because drug resistance is acquired by nonsynonymous substitution. Therefore, these substitutions can be regarded as the result of naturally occurring divergent evolution of these members. Synonymous substitution may thus be useful to deduce the natural relationship among pathogenic bacteria since they are not subjected to selection by antibiotics.
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M. tuberculosis complex-specific PCR and differentiation of the members by PCR-RFLP. A two-step method for differentiating the strains in the M. tuberculosis complex was developed. The first step involves detecting the M. tuberculosis complex, while the second step involves the differentiation of four species of the M. tuberculosis complex. The GyrB sequences of the M. tuberculosis complex were aligned with those of other mycobacterial species, and two unique sequences for the M. tuberculosis complex were found. A pair of primers, MTUB-f and MTUB-r, was then designed for specific amplification of the partial gyrB sequences from the M. tuberculosis complex. With these primers, the gyrB sequences were amplified from M. tuberculosis, but not from M. kansasii, M. gastri, M. abscessus, M. chelonae, or M. triviale (data not shown). The length of the amplified fragments was 1,020 bp. At the second step, the amplified DNA fragments were digested by RsaI or TaqI. As shown in Fig. 3B, M. bovis (lane 2) and M. microti (lane 5) could be differentiated from the other two species by the electrophorogram of the RsaI-digested fragments. Fragments of 500 and 700 bp can be found in the cases of M. bovis and M. microti, respectively, while 600-bp fragments were generated by RsaI digestion of the PCR products from M. tuberculosis and M. africanum. TaqI digestion of the M. tuberculosis gyrB fragment generated a 300-bp fragment, while a 150-bp fragment was generated from the other three species. Thus, RFLP analysis of the gyrB fragment could distinguish four species belonging to the M. tuberculosis complex.
Differentiation of members of the M. tuberculosis complex by species-specific PCR. We were also able to differentiate the members of the M. tuberculosis complex by species-specific PCR. We designed PCR primers that allowed selective amplification of the gyrB fragments from each species of the M. tuberculosis complex. The sequences and their positions are listed in Table 2. According to the designs of these primers, the gyrB fragment of M. tuberculosis could be amplified only by using the primer set of 756-G and 1410-C, the gyrB fragment of M. bovis could be amplified only by using the primer set of 756-A and 1410-A, the gyrB fragment of M. africanum could be amplified only by using the primer set of 756-G and 1410-A, and the gyrB fragment of M. microti could be amplified by using both the 756-G and 1450-A set and the 675-T and 1410-G set. Combination of these primers enabled four species of the M. tuberculosis complex to be differentiated (Fig. 3C).
gyrB sequences of clinically isolated M. tuberculosis strains. To evaluate the general applicability of the gyrB-based identification method, we analyzed the gyrB sequences of 18 M. tuberculosis strains isolated from patients, one M. bovis strain isolated from a cow, and the Japanese reference strain of BCG. Each M. tuberculosis strain was isolated from a different patient. They were classified into five different groups based on the variable numbers of tandem repeats in the ETR-A locus (7). Group 1 contained two strains (KPM KY590 and KPM 631), group 2 also contained two strains (KPM KY682 and KPM 721), and groups 3 and 4 each contained a single strain (KPM KY673 and KPM 679, respectively). The remaining 12 strains belonged to group 5. Thus, the strains studied were derived from at least five independent origins. The M. tuberculosis-specific substitutions found in the gyrB sequence of the type strain were conserved in all of the clinical isolates. Both the gyrB sequences of M. bovis isolated from a cow and the Japanese BCG strain were identical to that of the type strain of M. bovis, although the origins of these three strains were different. These results suggest that the synonymous substitutions found in M. tuberculosis and M. bovis are species specific. Besides these three common substitutions, we found three strain-specific base substitutions in the four M. tuberculosis strains. In the gyrB sequence of strain KPM KY673, the A at position 883 was found to be substituted by C, provoking the amino acid substitution from Ala to Pro. The A at position 1114 was found to be substituted by G in strain KPM KY679, while the G at position 1116 was found to be substituted by C in strains KPM KY678 and KPM H37Rv (GenBank accession number L27512). The latter two changes occurred in the same codon, ATG, provoking a change in the amino acid sequence from Met to Val or Ile. These two amino acid substitutions are found at positions that are highly conserved among the GyrB proteins of high G+C gram-positive bacteria. It is thus possible that the amino acid changes at these sites could confer some drug resistance to the strains.
Medical applications of gyrB sequences. Many clinically significant strains are classified as slowly growing mycobacteria. As shown in this study, more substitutions were found in the gyrB sequences than in the 16S rDNA and ITS sequences of slowly growing mycobacterial strains. With the benefit of higher base substitution frequencies, PCR or PCR-RFLP of gyrB could be used for the species identification of clinically isolated mycobacteria. These methods are highly applicable to clinical medicine because DNA sequencing is not required for rapid identification of these species.
The gyrB-based methods have already shown to be useful for differentiation of closely related strains of other bacteria, such as Vibrio (33) and Bacillus (39) spp. For quantitation analysis, too, the gyrB-based methods would be more useful than 16S rDNA-based methods because the copy number of gyrB is single in almost all of the bacteria examined (35, 36), while that of 16S rDNA is variable. We have determined the gyrB sequences of various bacteria and deposited them in the gyrB database (11), which recently became accessible via the internet (http://www.mbio.co.jp/icb/icb.html/). The sequence data accumulated in the gyrB database will be useful for the development of bacterial diagnostic systems based on molecular methods such as PCR, PCR-RFLP, and high-density DNA probe arrays (8, 30).| |
ACKNOWLEDGMENTS |
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We are grateful to Isao Kawamoto for helpful suggestions. We thank Yukiko Itazawa and Yuhka Takahashi for their technical assistance.
This work was performed as part of The Industrial Science and Technology Frontier Program supported by New Energy and Industrial Technology Development Organization.
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FOOTNOTES |
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* Corresponding author. Mailing address: Marine Biotechnology Institute, Kamaishi Laboratories, 3-75-1 Heita, Kamaishi, Iwate 026-0001, Japan. Phone: 81-193-26-6544. Fax: 81-193-26-6584/6592. E-mail: hiroaki.kasai{at}kamaishi.mbio.co.jp.
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Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References
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