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Previous Article | Next Article 
Antimicrobial Agents and Chemotherapy, October 2000, p. 2684-2688, Vol. 44, No. 10
Laboratoire de
Bactériologie-Virologie-Hygiène, CHU Dupuytren, 87042 Limoges,1 Unité des Agents
Antibactériens, Institut Pasteur, 75724 Paris Cedex
15,2 and Centre d'Etudes
Pharmaceutiques, 92296 Châtenay-Malabry,3
France
Received 15 December 1999/Returned for modification 28 March
2000/Accepted 1 July 2000
Twenty Acinetobacter baumannii strains resistant to
various antibiotics were analyzed for integron content and sequences of the amplification products. Sixteen clinical isolates had a class 1 integron, 2 contained an additional class 1 or class 2 integron, but no
class 3 integron was detected. Thirteen strains had integrons with a
single cassette: aac(3)-Ia (9 strains), ant(2")-Ia (2 strains), or aac(6')-Ib (2 strains); 1 had
aac(6')-Ib and oxa20
cassettes and an unknown gene; and 1 had an integron containing
ant(2")-Ia and an oxa3
cassette truncated by IS6100. The remaining strains harbored class 1 integrons with gene cassettes previously found in
Enterobacteriaceae. One integron had a hybrid structure
composed of intI2 and the 3' conserved segment of class 1 integrons. These data indicate that integrons play a major role in
multidrug resistance in Acinetobacter.
Integrons are genetic elements that
can integrate, by site-specific recombination, gene cassettes, usually
antibiotic resistance genes (5). Three main classes of
integrons have been described (22). All have a 5' conserved
segment, including an intI gene encoding an integrase and an
attI recombination site, but have distinct 3' conserved
segments. In the class 1 integrons, the 3' conserved segment includes
three open reading frames (ORFs) Bacterial strains.
Twenty clinical A. baumannii
strains isolated between 1992 and 1998 were collected because of their
multiresistance to antibiotics, in particular to aminoglycosides,
sulfonamides, chloramphenicol, and
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Molecular Characterization of Integrons in
Acinetobacter baumannii: Description of a Hybrid Class
2 Integron
ABSTRACT
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References
INTRODUCTION
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References
qacE
1, a
deletion derivative of the antiseptic resistance gene qacE; the sul1 sulfonamide resistance gene; and ORF5, of unknown
functionor tni genes, as in Tn402
(18). The second class of integrons was found in transposon
Tn7 and its derivatives, and its 3' conserved segment
contains five tns genes involved in the movements of the transposon. A single class 3 integron has been reported to date, but
its 3' conserved segment has not been characterized (2). Cassettes usually include a single ORF and, downstream, an
attC site which is an imperfect inverted repeat sequence
related to a 60-bp consensus sequence (4). The movements of
cassettes are catalyzed by the integrase, which can excise or integrate cassettes by site-specific recombination between two specific sequences, either attI and attC or two
attC sites. Cassette mobility results in the dissemination
of resistance genes, and more than 50 cassettes have been described for
gram-negative bacteria (5). This genetic flexibility allows
numerous cassette rearrangements under antibiotic selective pressure,
and study of these various assortments can lead to a better
understanding of integron evolution. Acinetobacter, in
particular Acinetobacter baumannii, is increasingly responsible for nosocomial infections in intensive care units and is
often resistant to multiple antibiotics (27). Integrons have
already been found in this species, but their cassette content has not
been fully characterized (3, 25). The aim of our study was
to search for the presence of the three classes of integrons in
multidrug-resistant A. baumannii clinical isolates and to
characterize their gene cassette assortments.
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References
-lactams (Table
1). Seventeen strains were isolated from French hospitals, 1 was from Greece, and 2 were from the Czech Republic. Bacteria were grown in brain heart infusion broth
(Biomerieux, Marcy l'Etoile, France) or on Mueller-Hinton agar
(Biomerieux). Susceptibility to ampicillin, ticarcillin,
ceftazidime, gentamicin, isepamicin, amikacin, tobramycin, kanamycin,
streptomycin, spectinomycin, rifampin, chloramphenicol, and sulfonamide
was tested by disk diffusion on Mueller-Hinton agar. The susceptibility
tests were interpreted according to Comité de l'Antibiogramme de
la Société Française de Microbiologie recommendations
(1). Incubations were done at 37°C.
TABLE 1.
Bacterial strains and plasmids
Preparation and analysis of DNA. Total DNA was prepared by using a Qiamp tissue kit (Qiagen, Inc., Chatworth, Calif.). Small- and large-scale plasmid DNAs were prepared as described previously (24). DNA for PCR was obtained by boiling as described previously (16). Electrophoresis was performed with an 0.8% agarose gel (GIBCO BRL, Cergy Pontoise, France) and a Tris-borate-EDTA buffer system.
Genetic techniques. Escherichia coli JM83 was transformed as described previously (24). Selective antibiotic concentrations were as follows: ampicillin, 100 µg/ml; and tobramycin, 10 µg/ml.
DNA techniques.
Integrons were screened for by PCR with
three sets of primers specific for the intI1,
intI2, and intI3 genes and mapped with primers
complementary to conserved segments (Table
2). When the 3' conserved segment was
missing, the cassettes were cloned with selection for antibiotic
resistance. Amplification was performed with 50-µl reaction mixtures
consisting of Taq or Pfu DNA polymerase buffer,
1.5 mM MgCl2, 200 µM deoxynucleoside triphosphates, 50 pmol of each primer (Isoprim, Toulouse, France), 1 U of Taq
or 2 U of Pfu DNA polymerase, and 25 ng of DNA by use of
model 9600 DNA thermal cycler (Perkin-Elmer Cetus, Norwalk, Conn.). The
PCR products were purified using a Qiaquick PCR purification kit
(Qiagen) as recommended by the manufacturer. For strains with two PCR
products, the two fragments were separated by agarose gel
electrophoresis and purified using a Qiaquick gel extraction kit
(Qiagen).
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DNA sequencing. The PCR-amplified and cloned fragments were sequenced by using the ABI PRISM dRhodamine terminator protocol as recommended by the manufacturer (Perkin-Elmer Applied Biosystems, Les Ulis, France). Products were analyzed with an ABI PRISM 310 automated DNA sequencing apparatus (Perkin-Elmer Applied Biosystems).
Computer analysis of sequence data. The nucleotide sequence analysis procedure was obtained online over the Internet at the National Center for Biotechnology Information website (http://www.ncbi.nlm.nih.gov).
Enzymes and chemicals. T4 DNA ligase (Pharmacia, St. Quentin-en-Yvelines, France) and restriction endonuclease BamHI (Boehringer, Meylan, France) were used according to the recommendations of the manufacturers. Tobramycin and ampicillin were obtained from Sigma Chemical Co. (St. Louis, Mo.). Deoxynucleoside triphosphates were obtained from Boehringer. Taq DNA polymerase was purchased from GIBCO BRL, and Pfu DNA polymerase was obtained from Stratagene Cloning Systems (La Jolla, Calif.). Antibiotic disks were obtained from Sanofi Diagnostics Pasteur (Marnes-la-Coquette, France).
Nucleotide sequence accession numbers. The 403-bp ORFO cassette from BM4426 (see Results and Discussion), the class 1 integron from BM4430, and the class 2 hybrid integron from BM4431 have been deposited in the GenBank data library (Los Alamos, N.Mex.) under accession no. AJ251519, AJ289190, and AJ289189, respectively.
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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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Detection of intI genes.
The presence of integrons
was detected by amplification of an internal fragment of the integrase
genes in 80% (16 of 20) of A. baumannii isolates (Table
3), indicating that these elements are
widely spread among multiresistant isolates of this species. Among the
20 clinical isolates, 16 contained an intI1 gene. The intI2 gene of class 2 integrons was detected in strain
BM4431, which also contained a class 1 integron. The intI3
gene was not found. Previous studies have reported a high frequency of
multiresistant gram-negative isolates containing integrons (8, 9,
12). Class 1 integrons were found in 68% of worldwide nosocomial
isolates of A. baumannii (25). A study of 100 clinical isolates of A. baumannii from Chilean hospitals
indicated that more than 50% of the isolates harbored an
intI1 or an intI2 gene (3).
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Mapping of class 1 integrons. The cassette assortments in all the strains were characterized by PCR with the 5'-CS and 3'-CS primers and by sequencing of the amplification products (Table 3). Thirteen strains had integrons containing a single cassette which encoded an AAC(3)-Ia, an AAC(6')-Ib, or an ANT(2") aminoglycoside-modifying enzyme. Previous studies reported integrons with a single cassette, often an ant(3")-Ia gene, in various gram-negative bacteria (8, 13, 23, 25). In this study, the ant(3")-Ia gene cassette was not detected alone, but nine strains had an integron, not reported so far, carrying only aac(3)-Ia. Most strains were resistant to both streptomycin and spectinomycin, suggesting an aminoglycoside adenylyltransferase activity. An ant(3")-Ia gene cassette (GenBank accession no. X12870) was detected only in strains BM4431 and BM4436. Although most ant(3")-Ia genes are known to be part of integron cassettes, these genes have also been found outside integrons, such as in R538-1 (6). Another explanation is that an ant(3")-Ia gene cassette was included in a large integron which could not be detected by our PCR protocol.
Total DNA from A. baumannii BM4436 yielded two PCR products. The first fragment, 1.3 kb, contained two known cassettes, dfrB1 and aadA6; the second fragment, approximately 4 kb, contained a new assortment of four known cassettes, ant(2"), cmlA1, oxa10, and ant(3")-Ia. The integron in BM4426 was found to contain three cassettes (Table 3). The upstream one, adjacent to the 5' conserved segment, was aac(6')-Ib. The most downstream one was the oxa20 gene, recently found in an integron from Pseudomonas aeruginosa (15). These two cassettes were separated by a 466-bp sequence containing an ORF, designated ORFO, of 362 bp and displaying no homology with known genes. ORFO was followed by an attC site, indicating that it was part of a cassette. Other ORFs of unknown functions have also been found in integrons (19). A. baumannii BM4426 and BM4436 contained, respectively, oxa20 and aadA6 cassettes, already described for P. aeruginosa (15), confirming that integrons may be transferred via plasmids and/or transposons between these two species.The integron in BM4430.
Class 1 integrons lacking a 3'
conserved segment have been reported (21). In our study, the
3' conserved segment was strongly linked to class 1 integrons, since it
was detected by PCR with primers ORFL and SulR in 15 out of 16 strains.
The deleted integron in the remaining strain, BM4430, was characterized
by cloning with selection for tobramycin resistance. Analysis of the
sequence of the 3.8-kb BamHI insert of the recombinant
plasmid obtained, pAT719, showed that the integron had an unusual
organization, with an ant(2") gene cassette and,
downstream, the first 51 bases of an oxa3 cassette (Fig.
1A). The oxa3 cassette was
truncated by a copy of IS6100, an insertion sequence found
in Mycobacterium fortuitum (11). In BM4430,
IS6100 was followed by a 14-bp sequence and a copy of
IS26 (14) and a portion of the tnpM
gene, proposed to encode a modulator protein which enhances
Tn21 transposition and suppresses the resolution of
cointegrate replicons in vivo (7). The location of the
tnpM gene in BM4430 is unusual compared to the structure of
the integron In2 of Tn21, in which this gene is located
between the intI1 and tnpR genes, upstream from
the 5' conserved segment (10). The lack of an amplification
product of PCR with primers intI1R and tnpL suggests that the sequence at the right end of the truncated tnpM gene is not the
beginning of a second integron.
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Mapping of class 2 integrons. A. baumannii BM4431 yielded two PCR products with primers specific for the intI1 and intI2 genes (Table 3). To characterize these integrons, multiplex PCR with primers 5'-CS and 3'-CS, specific for the class 1 integrons, and primers int2S and intCS2, specific for the class 2 integrons, was performed and yielded two amplification products. The first one, 500 bp, contained a class 1 integron with a single aac(3)-Ia cassette (Table 3). The second one, 2.5 kb, contained the intI2 gene and the dfrA1 and sat cassettes, which are usually part of class 2 integrons (26). The ant(3")-Ia (also called aadA1) cassette, located downstream from the sat cassette, is identical to those previously reported for class 1 integrons (GenBank accession no. X12870) and differed from the ant(3")-Ia cassette found in class 2 integrons (GenBank accession no. X03043). This gene contains the codon AGA instead of AGG at position 684, the codon GTC instead of GTT at position 750, and the additional triplet GAA at position 706. Downstream from these cassettes, we did not find the tns genes usually described for the 3' conserved segment of class 2 integrons, but we did find the first 56 bp of the 3' conserved segment of class 1 integrons.
To characterize the entire 3' segment in BM4431, amplification with primers aadAL and ORFR (Fig. 1B) was performed and yielded a 1.6-kb fragment. Sequence determination of this fragment showed that the 3' end of the integron in BM4431 contained the same ORFs as the 3' conserved segment of class 1 integrons, i.e., qacE1, sul1, and ORF5 (Fig. 1B).
This first report of a chimeric integron indicates that recombination
between class 1 and class 2 integrons may occur in nature and is of
interest in view of the evolution of integrons and their implication in
the natural engineering of bacterial genomes. This hybrid structure may
have resulted from cointegrate formation catalyzed by the IntI1
integrase between a class 2 integron and a class 1 integron with the
ant(3")-Ia cassette at the left end of
the 3' conserved segment. Another possibility involves RecA-dependent
homologous recombination between two copies of the
ant(3")-Ia cassette, which has been
found in both classes of integrons. Class 2 integrons have already been detected in Acinetobacter spp., but their structure has not
been characterized (3, 25).
Distribution of integrons among RAPD types. Eleven RAPD profiles were observed among the 20 clinical isolates (Table 3). Integrons containing the same organization of cassettes were found in various RAPD genotypes (Table 3), suggesting a horizontal transfer of integrons, also suspected in other studies (23, 25). Martinez-Freijo et al. (12) also found similar integrons irrespective of host species or geographic origin. In addition, the promoter sequences were mostly conserved, even in isolates from different countries with distinct selective pressure, suggesting that acquisition of resistance likely is due to transfer of entire integrons via plasmids and/or transposons rather than of individual cassettes. In contrast, certain strains with similar RAPD types (B and D) contained distinct integrons.
Conclusions. Many studies have reported the high prevalence of integrons in human clinical isolates (9, 12, 13, 23, 26, 27) as well as in strains of animal origin (20) or from aquatic ecosystems (21), suggesting the important role of integrons in the dissemination of antibiotic resistance genes in the environment. Detection of integrons was often based on PCR or hybridization experiments (3, 8, 9, 12). Systematic sequencing of the integrons allows complete description of the cassettes and the detection of unusual rearrangements. Of special interest is the hybrid integron resulting from a recombination event between class 1 and class 2 integrons.
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ACKNOWLEDGMENTS |
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We thank H. Giamarellou and M. Kettner for the gift of Acinetobacter strains.
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FOOTNOTES |
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* Corresponding author. Mailing address: Laboratoire de Bactériologie-Virologie-Hygiène, CHU Dupuytren, 2, Avenue Martin Luther King, 87042 Limoges Cedex, France. Phone: (33) (5) 55 05 61 66. Fax: (33) (5) 55 05 67 22. E-mail: marieploy{at}lemel.fr.
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