Previous Article | Next Article 
Journal of Clinical Microbiology, April 1999, p. 1197-1199, Vol. 37, No. 4
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
rpoB Mutations in Multidrug-Resistant
Strains of Mycobacterium tuberculosis Isolated in
Italy
G.
Pozzi,1,*
M.
Meloni,2
E.
Iona,3
G.
Orrù,1
O. F.
Thoresen,3
M. L.
Ricci,3
M. R.
Oggioni,1
L.
Fattorini,3 and
G.
Orefici3
Sezione di Microbiologia, Dipartimento di
Biologia Molecolare, Università di Siena,
Siena,1 Sezione di Microbiologia,
Dipartimento di Scienze Chirurgiche, Università di Cagliari,
Cagliari,2 and Laboratorio di
Batteriologia e Micologia Medica, Istituto Superiore di
Sanità, 00161 Rome,3 Italy
Received 6 August 1998/Returned for modification 21 October
1998/Accepted 21 December 1998
 |
ABSTRACT |
Mutations of rpoB associated with rifampin resistance
were studied in 37 multidrug-resistant (MDR) clinical strains of
Mycobacterium tuberculosis isolated in Italy. At least one
mutated codon was found in each MDR strain. It was always a single-base
substitution leading to an amino acid change. Nine different
rpoB alleles, three of which had not been reported before,
were found. The relative frequencies of specific mutations in this
sample were different from those previously reported from different
geographical areas, since 22 strains (59.5%) carried the mutated codon
TTG in position 531 (Ser
Leu) and 11 (29.7%) had GAC in position 526 (His
Asp).
 |
TEXT |
The emergence of multidrug-resistant
(MDR) strains of Mycobacterium tuberculosis poses a serious
problem in tuberculosis control and stresses the need for the
development of rapid and reliable diagnostic methods for drug
susceptibility testing in clinical isolates. Recent advances in the
understanding of the genetic basis of drug resistance have allowed for
the development of DNA-based methods for the detection of resistance to
antituberculosis drugs (for a review, see Musser
[10]). These methods can be used, in conjunction with
molecular typing (18), to elucidate the molecular
epidemiology of drug resistance in M. tuberculosis. Epidemiological data are essential for the development of diagnostic strategies and, by providing information on the geographical
distribution of resistant alleles, can help us understand whether
mutated alleles arise independently or are attributable, in certain
instances, to the spread of a genotype (6, 15). Mutations in
rpoB, the gene coding for the
subunit of the RNA
polymerase, are responsible for resistance to rifampin (RFM)
(10), a fundamental drug for the therapy of tuberculosis
(1). In this work we analyzed the mutations occurring in the
rpoB gene of MDR strains of M. tuberculosis isolated in Italy.
RFM-resistant strains.
MDR isolates of M. tuberculosis from hospitals in northern and central Italy were
collected from three clinical microbiology laboratories (Ospedale
Umberto I, Ancona; Ospedale di Careggi, Florence; and Ospedale
Forlanini, Rome). The 37 MDR strains that formed the object of this
investigation (Table 1) were from
different patients and were typed by DNA fingerprinting
(IS6110) (17) in order to avoid the inclusion of
identical strains responsible for outbreaks (data not shown). The MICs
for RFM and rifabutin (RFB) were determined in 7H11 agar
(4). Strains were considered resistant to RFM when MICs were
>1 µg/ml and resistant to RFB when MICs were >0.5 µg/ml. All MDR
strains were resistant to both RFM and RFB.
Sequencing of rpoB.
To investigate the mutations
associated to RFM resistance, a segment of the rpoB gene was
sequenced. Genomic DNA from heat-inactivated suspensions of M. tuberculosis cells was obtained with the QIAamp Tissue kit
(Qiagen). A 318-bp fragment of rpoB, from nucleotide 1807 to
nucleotide 2124 (GenBank accession no. U12205), was amplified by PCR
and sequenced by a nonradioactive manual method (Silver Sequence DNA
sequencing system; Promega). The same primers (5'-CGA TCA CAC CGC AGA
CGT TG-3' and 5'-GGT ACG GCG TTT CGA TGA AC-3') were used for PCR and
DNA sequencing. Both DNA strands were sequenced, each using as a
template the product of a different PCR. At least one mutated codon was
found in each RFM-resistant strain; it was always a single-base
substitution leading to an amino acid change. Nine different
rpoB alleles were found, five with one mutation (33 strains
[89.1%]), three with three mutations (3 strains [8.1%]), and one
with two mutations (1 strain [2.7%]) (Table
2). The mutated allele carrying the TTG
codon in position 531 was the most common (56.7%), together with the
one carrying GAC in position 526 (24.3%). Three new alleles, those
with three mutated codons, were recognized in this investigation (Table
2). Mutations already reported in the literature were found in codons 511, 512, 516, 526, and 531. In two strains we also found four new
mutations: in codons 523 (TGG) and 525 (ATC) in one strain (GenBank
accession no. AF055891) and in codons 541 (GAT) and 553 (CGC) in the
other (GenBank accession no. AF055892). Twenty-two strains (59.5%)
carried the mutated codon TTG in position 531 (Ser
Leu), and 11 strains (29.7%) had GAC in position 526 (His
Asp). A total of 34 of
37 strains (91.9%) had mutations in position 531 and/or position 526.
In this study on MDR strains of
M. tuberculosis from
northern and central Italy, RFM resistance was always found associated
with RFB resistance, and in each strain we could detect the presence
of
a mutated
rpoB allele. By comparing our data with the
literature
(Fig.
1), we observed that the
two mutations occurring most frequently
in Italian strains (531TTG and
526GAC) have different relative
frequencies in strains from different
countries. While 531TTG
is absolutely the most common mutation
worldwide, 526GAC appears
to be prevalent in only a few countries,
including Italy, Greece,
and Mozambique. Among the possible
explanations, transmission
of MDR strains among patients could account
for the disequilibrium
in the geographical distributions of
rpoB mutations. Of course,
genetic-exchange mechanisms
responsible for the spread of resistant
alleles in
M. tuberculosis cannot be completely ruled out, even
if, due to the
current understanding of mycobacterial genetics,
they would be more
difficult to postulate.

View larger version (22K):
[in this window]
[in a new window]
|
FIG. 1.
Comparison of the relative frequencies of
rpoB mutations in RFM-resistant M. tuberculosis
strains from different countries. The mutated codons TTG in position
531 (A) and GAC in position 526 (B) represent the two most frequent
mutations in Italian strains. Data reported here are from the present
study (for Italy) and from the literature for Germany (15),
Greece (7), Sierra Leone (15), Japan (12,
13, 16), the United States (3, 6, 8, 11), Mozambique
(2), and "different sources" a (9), b
(17), c (19), and d (4). The number of
strains in which the mutation was found/total number of strains studied
is given in each bar.
|
|
Nucleotide sequence accession numbers.
The new alleles found
in this study have been deposited in GenBank under accession no.
AF055891, AF055892, and AF055893.
 |
ACKNOWLEDGMENTS |
We thank P. Chiaradonna, C. Piersimoni, E. Tortoli, and M. Tronci
for providing clinical strains and valuable advice.
This study was supported by grants from the Istituto Superiore di
Sanità (Progetto Nazionale Tubercolosi, no. 96/D/T55).
 |
FOOTNOTES |
*
Corresponding author. Mailing address:
Microbiologia/Università di Siena, Via Laterina 8, 53100 Siena,
Italy. Phone: 39-0577-263874. Fax: 39-0577-263870. E-mail:
pozzi{at}unisi.it.
 |
REFERENCES |
| 1.
|
Bass, J. B., Jr.,
L. S. Farer,
P. C. Hopewell,
R. O'Brien,
R. F. Jacobs,
F. Ruben,
D. E. Snider, Jr., and G. Thornton, Jr.
1994.
Treatment of tuberculosis and tuberculosis infection in adults and children. American Thoracic Society and The Centers for Disease Control and Prevention.
Am. J. Respir. Crit. Care Med.
149:1359-1374[Abstract].
|
| 2.
|
Caugant, D. A.,
P. Sandven,
J. Eng,
J. T. Jeque, and T. Tonium.
1995.
Detection of rifampin resistance among isolates of Mycobacterium tuberculosis from Mozambique.
Microb. Drug Resist.
1:321-326.
[Medline] |
| 3.
|
Cooksey, R. C.,
G. P. Morlock,
S. Glickman, and J. T. Crawford.
1997.
Evaluation of a line probe assay kit for characterization of rpoB mutations in rifampin-resistant Mycobacterium tuberculosis isolates from New York City.
J. Clin. Microbiol.
35:1281-1283[Abstract].
|
| 4.
|
Heifets, L. B.
1991.
Antituberculosis drugs: antimicrobial activity in vitro, p. 14-49.
In
L. B. Heifets (ed.), Drug susceptibility in the chemotherapy of mycobacterial infections. CRC Press Inc., Boca Raton, Fla.
|
| 5.
|
Heym, B.,
N. Honore,
C. Pernot-Truffot,
A. Banerjee,
C. Schurra,
W. R. Jacobs, Jr.,
J. D. A. van Embden,
J. H. Grosset, and S. T. Cole.
1998.
Implications of multidrug resistance for the future of short-course chemotherapy of tuberculosis: a molecular study.
Lancet
344:293-298.
|
| 6.
|
Kapur, V.,
L.-L. Li,
S. Iordanescu,
M. R. Hamrick,
A. Wanger,
B. N. Kreiswirth, and J. M. Musser.
1994.
Characterization by automated DNA sequencing of mutations in the gene (rpoB) encoding the RNA polymerase b subunit in rifampin-resistant Mycobacterium tuberculosis strains from New York City and Texas.
J. Clin. Microbiol.
32:1095-1098[Abstract/Free Full Text].
|
| 7.
|
Matsiota-Bernard, P.,
G. Vrioni, and E. Marinis.
1998.
Characterization of rpoB mutations in rifampin-resistant clinical Mycobacterium tuberculosis isolates from Greece.
J. Clin. Microbiol.
36:20-23[Abstract/Free Full Text].
|
| 8.
|
Moghazeh, S. L.,
X. Pan,
T. Arain,
C. K. Stover,
J. M. Musser, and B. N. Kreiswirth.
1996.
Comparative antimycobacterial activities of rifampin, rifampentine, and KRM-1648 against a collection of rifampin-resistant Mycobacterium tuberculosis isolates with known rpoB mutations.
Antimicrob. Agents Chemother.
40:2655-2657[Abstract].
|
| 9.
|
Morris, S.,
G. H. Bai,
P. Suffys,
L. Gomez-Portillo,
M. Fairchok, and D. Rouse.
1995.
Molecular mechanisms of multiple drug resistance in clinical isolates of Mycobacterium tuberculosis.
J. Infect. Dis.
171:954-960[Medline].
|
| 10.
|
Musser, J. M.
1995.
Antimicrobial agent resistance in mycobacteria: molecular genetic insights.
Clin. Microbiol. Rev.
8:496-514[Abstract].
|
| 11.
|
Nachamkin, I.,
C. Kang, and M. P. Weinstein.
1997.
Detection of resistance to isoniazid, rifampin, and streptomycin in clinical isolates of Mycobacterium tuberculosis by molecular methods.
Clin. Infect. Dis.
24:894-900[Medline].
|
| 12.
|
Ohno, H.,
H. Koga,
S. Kohno,
T. Tashiro, and K. Hara.
1996.
Relationship between rifampin MICs for rpoB mutations of Mycobacterium tuberculosis strains isolated in Japan.
Antimicrob. Agents Chemother.
40:1053-1056[Abstract].
|
| 13.
|
Ohno, H.,
H. Koga,
T. Kuroita,
K. Tomono,
K. Ogawa,
K. Yanagihara,
Y. Yamamoto,
J. Miyamoto,
T. Tashiro, and S. Kohno.
1997.
Rapid prediction of rifampin susceptibility of Mycobacterium tuberculosis.
Am. J. Respir. Crit. Care Med.
155:2057-2063[Abstract].
|
| 14.
|
Ovchinnikov, Y. A.,
G. S. Monastyrskaya,
V. V. Gubanov,
S. O. Guryev,
O. Y. Chertov,
N. N. Modyanov,
V. A. Grinkevich,
I. A. Makarova,
T. V. Marchenko,
I. N. Polovnikova, et al.
1981.
The primary structure of Escherichia coli RNA polymerase. Nucleotide sequence of the rpoB gene and amino-acid sequence of the beta-subunit.
Eur. J. Biochem.
116:621-629[Medline].
|
| 15.
|
Rinder, H.,
P. Dobner,
K. Feldmann,
M. Rifai,
G. Bretzel,
S. Rusch-Gerdes, and T. Loscher.
1997.
Disequilibria in the distribution of rpoB alleles in rifampicin-resistant M. tuberculosis isolates from Germany and Sierra Leone.
Microb. Drug Resist.
3:195-197.
[Medline] |
| 16.
|
Taniguchi, H.,
H. Aramaki,
Y. Nikaido,
Y. Mizuguchi,
M. Nakamura,
T. Koga, and S.-I. Yoshida.
1996.
Rifampicin resistance and mutation of rpoB in Mycobacterium tuberculosis.
FEMS Microbiol. Lett.
144:103-108[Medline].
|
| 17.
|
Telenti, A.,
P. Imboden,
F. Marchesi,
D. Lowrie,
S. Cole,
M. J. Colston,
L. Matter,
K. Schopfer, and T. Bodmer.
1993.
Detection of rifampicin-resistance mutations in Mycobacterium tuberculosis.
Lancet
341:647-650[Medline].
|
| 18.
|
van Soolingen, D.,
P. E. W. de Haas,
P. W. M. Hermans, and J. D. A. van Embden.
1994.
DNA fingerprinting of Mycobacterium tuberculosis.
Methods Enzymol.
235:196-205[Medline].
|
| 19.
|
Williams, D. L.,
C. Waguespack,
K. Eisenach,
J. T. Crawford,
F. Portaels,
M. Salfinger,
C. M. Nolan,
C. Abe,
V. Sticht-Groh, and T. P. Gillis.
1994.
Characterization of rifampin resistance in pathogenic mycobacteria.
Antimicrob. Agents Chemother.
38:2380-2386[Abstract/Free Full Text].
|
Journal of Clinical Microbiology, April 1999, p. 1197-1199, Vol. 37, No. 4
0095-1137/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
This article has been cited by other articles:
-
Ebrahim, G. J.
(2007). Drug Resistance in Tuberculosis. J Trop Pediatr
53: 147-149
[Full Text]
-
Miotto, P., Piana, F., Penati, V., Canducci, F., Migliori, G. B., Cirillo, D. M.
(2006). Use of Genotype MTBDR Assay for Molecular Detection of Rifampin and Isoniazid Resistance in Mycobacterium tuberculosis Clinical Strains Isolated in Italy.. J. Clin. Microbiol.
44: 2485-2491
[Abstract]
[Full Text]
-
Meacci, F., Orru, G., Iona, E., Giannoni, F., Piersimoni, C., Pozzi, G., Fattorini, L., Oggioni, M. R.
(2005). Drug Resistance Evolution of a Mycobacterium tuberculosis Strain from a Noncompliant Patient. J. Clin. Microbiol.
43: 3114-3120
[Abstract]
[Full Text]
-
O'Sullivan, D. M., McHugh, T. D., Gillespie, S. H.
(2005). Analysis of rpoB and pncA mutations in the published literature: an insight into the role of oxidative stress in Mycobacterium tuberculosis evolution?. J Antimicrob Chemother
55: 674-679
[Abstract]
[Full Text]
-
Jou, R., Chen, H.-Y., Chiang, C.-Y., Yu, M.-C., Su, I.-J.
(2005). Genetic Diversity of Multidrug-Resistant Mycobacterium tuberculosis Isolates and Identification of 11 Novel rpoB Alleles in Taiwan. J. Clin. Microbiol.
43: 1390-1394
[Abstract]
[Full Text]
-
Yam, W. C., Tam, C. M., Leung, C. C., Tong, H. L., Chan, K. H., Leung, E. T. Y., Wong, K. C., Yew, W. W., Seto, W. H., Yuen, K. Y., Ho, P. L.
(2004). Direct Detection of Rifampin-Resistant Mycobacterium tuberculosis in Respiratory Specimens by PCR-DNA Sequencing. J. Clin. Microbiol.
42: 4438-4443
[Abstract]
[Full Text]
-
Mokrousov, I., Otten, T., Vyshnevskiy, B., Narvskaya, O.
(2003). Allele-Specific rpoB PCR Assays for Detection of Rifampin-Resistant Mycobacterium tuberculosis in Sputum Smears. Antimicrob. Agents Chemother.
47: 2231-2235
[Abstract]
[Full Text]
-
Dreses-Werringloer, U., Padubrin, I., Kohler, L., Hudson, A. P.
(2003). Detection of Nucleotide Variability in rpoB in both Rifampin-Sensitive and Rifampin-Resistant Strains of Chlamydia trachomatis. Antimicrob. Agents Chemother.
47: 2316-2318
[Abstract]
[Full Text]
-
Yue, J., Shi, W., Xie, J., Li, Y., Zeng, E., Wang, H.
(2003). Mutations in the rpoB Gene of Multidrug-Resistant Mycobacterium tuberculosis Isolates from China. J. Clin. Microbiol.
41: 2209-2212
[Abstract]
[Full Text]
-
Van Der Zanden, A. G. M., Te Koppele-Vije, E. M., Vijaya Bhanu, N., Van Soolingen, D., Schouls, L. M.
(2003). Use of DNA Extracts from Ziehl-Neelsen-Stained Slides for Molecular Detection of Rifampin Resistance and Spoligotyping of Mycobacterium tuberculosis. J. Clin. Microbiol.
41: 1101-1108
[Abstract]
[Full Text]
-
Hwang, H.-Y., Chang, C.-Y., Chang, L.-L., Chang, S.-F., Chang, Y.-H., Chen, Y.-J.
(2003). Characterization of rifampicin-resistant Mycobacterium tuberculosis in Taiwan. J Med Microbiol
52: 239-245
[Abstract]
[Full Text]
-
Fattorini, L., Tan, D., Iona, E., Mattei, M., Giannoni, F., Brunori, L., Recchia, S., Orefici, G.
(2003). Activities of Moxifloxacin Alone and in Combination with Other Antimicrobial Agents against Multidrug-Resistant Mycobacterium tuberculosis Infection in BALB/c Mice. Antimicrob. Agents Chemother.
47: 360-362
[Abstract]
[Full Text]
-
Cavusoglu, C., Hilmioglu, S., Guneri, S., Bilgic, A.
(2002). Characterization of rpoB Mutations in Rifampin-Resistant Clinical Isolates of Mycobacterium tuberculosis from Turkey by DNA Sequencing and Line Probe Assay. J. Clin. Microbiol.
40: 4435-4438
[Abstract]
[Full Text]
-
Qian, L., Abe, C., Lin, T.-P., Yu, M.-C., Cho, S.-N., Wang, S., Douglas, J. T.
(2002). rpoB Genotypes of Mycobacterium tuberculosis Beijing Family Isolates from East Asian Countries. J. Clin. Microbiol.
40: 1091-1094
[Abstract]
[Full Text]
-
Bartfai, Z., Somoskovi, A., Kodmon, C., Szabo, N., Puskas, E., Kosztolanyi, L., Farago, E., Mester, J., Parsons, L. M., Salfinger, M.
(2001). Molecular Characterization of Rifampin-Resistant Isolates of Mycobacterium tuberculosis from Hungary by DNA Sequencing and the Line Probe Assay. J. Clin. Microbiol.
39: 3736-3739
[Abstract]
[Full Text]
-
Fines, M., Pronost, S., Maillard, K., Taouji, S., Leclercq, R.
(2001). Characterization of Mutations in the rpoB Gene Associated with Rifampin Resistance in Rhodococcus equi Isolated from Foals. J. Clin. Microbiol.
39: 2784-2787
[Abstract]
[Full Text]
-
Mani, C., Selvakumar, N., Narayanan, S., Narayanan, P. R.
(2001). Mutations in the rpoB Gene of Multidrug-Resistant Mycobacterium tuberculosis Clinical Isolates from India. J. Clin. Microbiol.
39: 2987-2990
[Abstract]
[Full Text]
-
Van Rie, A., Warren, R., Mshanga, I., Jordaan, A. M, van der Spuy, G. D., Richardson, M., Simpson, J., Gie, R. P., Enarson, D. A., Beyers, N., van Helden, P. D., Victor, T. C.
(2001). Analysis for a Limited Number of Gene Codons Can Predict Drug Resistance of Mycobacterium tuberculosis in a High-Incidence Community. J. Clin. Microbiol.
39: 636-641
[Abstract]
[Full Text]
-
Heep, M., Brandstätter, B., Rieger, U., Lehn, N., Richter, E., Rüsch-Gerdes, S., Niemann, S.
(2001). Frequency of rpoB Mutations Inside and Outside the Cluster I Region in Rifampin-Resistant Clinical Mycobacterium tuberculosis Isolates. J. Clin. Microbiol.
39: 107-110
[Abstract]
[Full Text]
-
Morlock, G. P., Plikaytis, B. B., Crawford, J. T.
(2000). Characterization of Spontaneous, In Vitro-Selected, Rifampin-Resistant Mutants of Mycobacterium tuberculosis Strain H37Rv. Antimicrob. Agents Chemother.
44: 3298-3301
[Abstract]
[Full Text]
-
Reynolds, M. G.
(2000). Compensatory Evolution in Rifampin-Resistant Escherichia coli. Genetics
156: 1471-1481
[Abstract]
[Full Text]