Antimicrobial Agents and Chemotherapy, December 1998, p. 3053-3058, Vol. 42, No. 12
Laboratory of Cellular
Biology1 and
Laboratory of Bacteriology
and Medical Mycology,2
Istituto
Superiore di Sanità Rome, and Institute of Microbiology,
University of Rome, "La Sapienza,"3 Rome,
Italy
Received 10 March 1998/Returned for modification 7 July
1998/Accepted 9 September 1998
The presence and genetic content of integrons were investigated for
37 epidemiologically unrelated multiple-drug-resistant strains of
Salmonella enterica serotype Typhimurium from humans. All
isolates were resistant to ampicillin, chloramphenicol, kanamycin, streptomycin, sulfonamides, and trimethoprim, as well as to
tetracycline and/or nalidixic acid; 20% of them were also resistant to
gentamicin and amikacin. Three different class 1 integrons (In-t1,
In-t2, and In-t3) were identified by Southern blot hybridization, PCR, and DNA sequencing, and these integrons were found to carry the aadB, catB3, oxa1,
aadA1a, aacA4, and aacC1 gene
cassettes. Integrons In-t1 (aadB and catB3) and
In-t2 (oxa1 and aadA1a) were both located on a
conjugative IncFI plasmid of 140 kb. In-t3 (aacA4,
aacC1, and aadAIa) was located on an IncL/M
plasmid of 100 kb which was present, in association with the IncFI
plasmid, in gentamicin- and amikacin-resistant isolates. Despite the
extensive similarity at the level of the antibiotic resistance
phenotype, integrons were not found on the prototypic IncFI plasmids
carried by epidemic Salmonella strains isolated during the
late 1970s. The recent appearance and the coexistence of multiple
integrons on two conjugative plasmids in the same
Salmonella isolate are examples of how mobile gene
cassettes may contribute to the acquisition and dissemination of
antibiotic resistance.
Bacterial resistance to antimicrobial
agents is a serious problem worldwide, and understanding of the
molecular basis of how resistance genes are acquired and transmitted
may contribute to the creation of new antimicrobial strategies
(47). One efficient mechanism for the acquisition and
dissemination of resistance determinants is their transmission through
mobile genetic elements. It has been proposed that promiscuous
plasmids, conjugative transposons, and transposons carried by
conjugative plasmids are responsible for the horizontal spread of
resistance genes throughout bacteria (9). Recently,
naturally occurring gene expression elements called "integrons"
have been described as vehicles for the acquisition of resistance genes
carried by mobile elements (14, 26, 46). These structures
have also been found to be involved in the genetic reassortment of
resistance determinants frequently observed in multiple-antibiotic-resistant bacterial pathogens (5).
Three classes of integrons have been identified. Class 1 integrons are
prevalent among clinical isolates and are composed of two conserved
regions, the 5'CS and the 3'CS regions, surrounding an interposed
variable region (14, 16). The variable region contains gene
cassettes for antibiotic resistance integrated, all in the same
orientation, at the attI site. Coordinate expression of the
gene cassettes is driven by the tandemly arranged
Pant and P2 promoters (39). The 5'CS
region of class 1 integrons contains the intI1 gene, which
encodes the type 1 integrase protein, which is responsible for
site-specific insertion and excision of gene cassettes (5).
As a consequence of this activity, integrons exist in a large variety
of forms with respect to the number, type, and order of the inserted
genes. Each gene cassette includes an open reading frame and a
recombination site known as the "59-base element" located
downstream of each coding sequence (15). The 3'CS contains
the sul1 and the qacE The occurrence of integrons among clinical bacterial isolates is under
investigation, and recent studies report a widespread distribution of
these elements among multiple-antibiotic-resistant nosocomial bacteria
(18, 20, 34).
Salmonella enterica serotype Typhimurium is one of the more
frequent agents of bacterial enteritis worldwide (29). This serotype has often been described as being resistant to multiple drugs,
most commonly showing resistance to ampicillin (Ap), chloramphenicol (Cm), streptomycin (Sm), sulfonamides (Su), and tetracycline (Te). The
R types R-ApCmSmSuTe and R-ApSmSuTe have been associated with the
phage types DT104 and DT193, respectively (17, 23, 48).
In the study described in this report, we investigated the genetic
determinants for antibiotic resistance of S. enterica
serotype Typhimurium strains isolated from epidemiologically unrelated pediatric patients with gastroenteritis. Our results indicate that the
multiple-drug resistance phenotype is determined by integrons carrying
an unusually wide repertoire of resistance gene cassettes. Up to three
types of integrons located on two conjugative plasmids were identified.
The quality, number, and organization of the resistance genes were then determined.
Bacterial strains.
Thirty-seven S. enterica
serotype Typhimurium strains were isolated from the stools of children
hospitalized for acute gastroenteritis at the Pediatric Clinic of the
University of Tirana (Tirana, Albania) from June 1996 to February 1997 and were sent to the Laboratory of Bacteriology and Medical Mycology of
the Istituto Superiore di Sanità in Rome, Italy, for
characterization. All patients originated from different districts of Albania.
0066-4804/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Class 1 Integron-Borne Multiple-Antibiotic
Resistance Carried by IncFI and IncL/M Plasmids in Salmonella
enterica Serotype Typhimurium
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ABSTRACT
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
![]()
INTRODUCTION
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
1 genes, which confer
resistance to sulfonamides and to quaternary ammonium compounds,
respectively (33, 36). Gene cassette arrays similar to those
of the class 1 integrons were observed for the transposon
Tn7 and its close relatives, forming a second class of
integrons. A putative defective integrase gene (intI2),
whose product is 40% identical to that of intI1, is located
in the distal portion of Tn7 (11). Recently, a
third class of integron has been identified, and the putative integrase
(intI3), located at the 5' of the
blaIMP cassette, is 61% identical to the
intI1 integrase (31).
![]()
MATERIALS AND METHODS
Top
Abstract
Introduction
Materials & Methods
Results
Discussion
References
Antimicrobial susceptibility and transfer of resistance. S. enterica serotype Typhimurium isolates were preliminarily tested for antibiotic resistance by the disk diffusion assay on Mueller-Hinton agar with commercial antimicrobial susceptibility disks (Oxoid, Basingstoke, United Kingdom, and Becton Dickinson Microbiological System, Cockeysville, Md.) according to the recommendations of the National Committee for Clinical Laboratory Standards (30).
The rifampin-resistant mutant strain Escherichia coli K-12 CSH26-R was used as the recipient in conjugation experiments (24). Exconjugants were selected on Luria-Bertani agar containing 100 µg of rifampin per ml plus 20 µg of amikacin (Ak) per ml or 30 µg of chloramphenicol per ml and were tested on Simmons citrate-agar plates (Biogenetics, Padova, Italy) to distinguish exconjugants from spontaneous rifampin-resistant donor mutants. Intraspecific matings were performed with the nalidixic acid (Na)-resistant strain E. coli CSH26-N as the recipient.Characterization of plasmids and identification of integrons by DNA hybridization. Plasmid DNA was extracted by the procedure of Kado and Liu (21), electrophoresed in a 0.8% agarose gel at 5 V/cm, and stained with ethidium bromide.
Extraction of genomic DNA and colony hybridizations were performed as described elsewhere (10, 41). Plasmid DNA, digested genomic DNA, and bacterial colonies were transferred onto a positively charged nylon membrane (Boehringer Mannheim, Mannheim, Germany) by standard methods (41) and were hybridized under high-stringency conditions with a specific probe for integrase genes intI1 and intI2. The intI1 probe was obtained by restriction and agarose elution of the 596-bp PvuII-RsaI fragment from the transposon-carrying plasmid pACYC184::Tn21 (7). The intI2 probe was obtained by PCR amplification on R483::Tn7 (45) with primers intI2A and intI2B (Table 1) internal to the released intI2 sequence. DNA fragments were labelled with [
-32P]dCTP with a random labelling kit (Bethesda
Research Laboratories, Inc., Gaithersburg, Md.).
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PCR amplification, cloning, and sequencing of integrons.
Amplification reactions were carried out by PCR with 10 µl of boiled
bacterial suspensions, with 200 µM deoxynucleoside triphosphate, 1 µM the primer pairs listed in Table 1, Taq Plus buffer
(Promega), and 5 U of Taq Plus polymerase (Stratagene). The
PCR was run at 94°C for 30 s, 59°C for 30 s, and 72°C
for 3.5 min for a total of 35 cycles. Amplicons were blunt-end ligated
at the SmaI site of the pGEM 3z(f+) vector (Promega) and
were used to transform E. coli DH5
cells (41).
Sequencing reactions were performed with double-stranded plasmid
preparations by the dideoxy chain termination method with universal
primers (43) and a commercial kit purchased from Pharmacia
Biotech and products were analyzed with a Pharmacia Biotech ALFexpress
automated DNA sequencing apparatus. The presence of the
sul-1 gene was investigated by PCR amplification with the
primers described by Sandvang et al. (42).
Nucleotide sequence accession numbers. The nucleotide sequences of In-t1, In-t2, and In-t3 have been assigned EMBL accession nos. AJ009818, AJ009819, and AJ009820, respectively.
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RESULTS |
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Antibiotic resistance profiles and characterization of plasmids of S. enterica serotype Typhimurium isolates. Thirty-seven S. enterica serotype Typhimurium isolates of human origin were tested for antimicrobial susceptibility. All strains were resistant to ampicillin, chloramphenicol, kanamycin (Km), streptomycin, sulfonamides, and trimethoprim (Tp). Additionally, 75% of the isolates were also resistant also to tetracycline, 38% were also resistant to nalidixic acid, and 20% were also resistant to amikacin and gentamicin (Gm).
Plasmids from six Salmonella strains were examined (Table 2). The approximate sizes of the Salmonella plasmids were estimated by direct comparison with three reference plasmids harbored by the multi-drug-resistant strain S. enterica Wien WZM6 (R-ApCmKmSmSuTe) (24). This strain carries an IncFI plasmid of 140 kb (pZM61; R-ApCmKmTe) and two smaller plasmids of 13 kb (pZM62; R-ApSmSu) and 2.1 kb (pZM63 [a cryptic plasmid]; Fig. 1A, lane 1). S. enterica serotype Typhimurium strains 44, 516, 252 (Fig. 1A, lanes 2, 3, and 4), 298, 202 (Fig. 1A, lanes 5 and 6), and 341 (Fig. 1A, lane 7) all carried a large plasmid similar in size to pZM61. Strains 202 and 298, representative of the R-ApCmKmSmSuTpTeGmAk type, carried an additional large plasmid of approximately 100 kb. Other smaller heterogeneous plasmids were present in all strains (27).
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Transfer of resistance. Prototypic Salmonella strains 366, 341, 252, 202, and 298 were conjugated with E. coli CSH26-R. Two types of exconjugants were obtained from strains 202 and 298 upon selection on rifampin-amikacin and rifampin-chloramphenicol plates: the Ak-type exconjugants of the R-ApKmSuGmAk type and the Cm-type exconjugants of the R-ApCmKmSmSuTmTe type. Cm-type exconjugants were also obtained from strains 366, 341, and 252 (Table 2).
Transconjugants were examined for their plasmid profiles. We found that all Cm-type transconjugants harbored the IncFI plasmid, while the Ak-type transconjugants carried the IncL/M replicon. Figure 2A illustrates the independent transmission of the two plasmids from S. enterica serotype Typhimurium 202 to E. coli. Both Cm and Ak types of transconjugants were able to transfer their complete R patterns in intraspecific matings with E. coli CSH26-N as the recipient strain, showing transfer frequencies comparable to those observed in interspecific matings (data not shown).
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Integrons in S. enterica serotype Typhimurium plasmids. The presence of the sulfonamide resistance determinant is strongly suggestive of the presence of class 1 integrons when it is carried by conjugative plasmids (36). Therefore, we analyzed the IncFI and IncL/M plasmids harbored by S. enterica serotype Typhimurium for the presence of these genetic elements. We initially searched for the presence of the class 1 integrase gene, and Southern hybridization experiments were carried out with plasmid DNA by using the intI1 probe. Plasmid pACYC184::Tn21 carrying the Tn21 integron was used as the positive control (Fig. 1A, lane 8). Figure 1E (lanes 2 to 7) shows that the 140-kb IncFI plasmid of all representative strains and the 100-kb IncL/M plasmid carried by strains 202 and 298 hybridize with the integrase gene (intI1) probe. Interestingly, none of the S. enterica serotype Wien WZM6 plasmids were found to be positive when they were probed for the presence of the class 1 integrase gene (Fig. 1E, lane 1).
Of note, three additional multi-drug-resistant epidemic S. enterica serotype Wien strains (W537, W811, and W569; R-ApCmKmTe, R-ApCmKmSmTe, and R-ApCmSuTpGmNa, respectively) isolated in Italy at the Istituto Superiore di Sanità during the period from 1983 to 1989 were also negative by colony hybridization for the intI1 gene. Conversely, the presence of class 1 integrons was demonstrated by colony hybridization with the intI1 probe in all 37 multi-drug-resistant S. enterica serotype Typhimurium isolates (data not shown). To better characterize the integronic structures associated with S. enterica serotype Typhimurium conjugative plasmids, we performed a PCR analysis with the 5'CS and 3'CS primers (22) with DNA extracted from the strain 202 Cm-type and strain 202 Ak-type transconjugants, as well as from the donor S. enterica serotype Typhimurium 202 isolate. The results showed the presence in S. enterica serotype Typhimurium 202 of three types of integrons, which we designated In-t1, In-t2, and In-t3, respectively; they carried variable regions of 1.5, 2.1, and 3.2 kb, respectively (Fig. 2B, lane 1). These three integrons were conjugatively transferable by the two IncFI and IncL/M plasmids. In fact, the Cm-type transconjugant, which had acquired the IncFI plasmid, generated both In-t1 and In-t2 amplicons (Fig. 2B, lane 3). Moreover, the 3.2-kb DNA band, corresponding to In-t3, was generated by the Ak-type exconjugant which had received the IncL/M plasmid only (Fig. 2B, lane 2). The recipient strain E. coli CSH26-R was negative by PCR for the class 1 integrons (data not shown). Southern blot analysis of BamHI- and PvuII-digested total DNA from prototypic multi-drug-resistant S. enterica serotype Typhimurium isolates confirmed the existence of all three types of integrons carrying the variable regions revealed by PCR and allowed us to rule out the possibility that class 1 integrons other than those identified on the IncFI and IncL/M plasmids were present in these isolates (data not shown). In addition, the presence of class 2 and 3 integrons in these isolates was ruled out by Southern blot analysis and amplification reactions performed with intI3-specific primers intI3A and intI3B (Table 1).Integron-borne gene cassettes.
The In-t1, In-t2, and In-t3 PCR
products were cloned in pGem 3Zf(+) and were entirely sequenced (Fig.
3). The nucleotide sequence of In-t1 showed
the presence of two gene cassettes, the aadB gene [also
named ant(2")-Ia] and the catB3 gene. The
aadB gene cassette is 596 bp long and encodes the enzyme
aminoglycoside adenyltransferase AAD(2"). This enzyme has been shown to
confer resistance to kanamycin and to low levels of gentamicin
(44). The catB3 gene corresponds to an open
reading frame of 633 bp which encodes the enzyme chloramphenicol acetyltransferase (CatB3) (2). On the basis of a sequence
comparison, the putative Pant promoter was found to consist
of a
35 signal (TGGAGA) separated by 17 bases from a
10
signal (TAAGCT). The secondary promoter P2 was also
identified ca. 80 nucleotides downstream of Pant and was
found to consist of the sequence
35TTGTTA-[N17]-
10TACAGT
(6).
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35TTGACA-[N17]-
10TAAACT
element. The P2 promoter was identical in sequence and location to
those found in In-t1 and In-t2.
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DISCUSSION |
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In this report we describe the presence of multiple class 1 integrons conferring resistance to a very broad spectrum of antibiotics in S. enterica serotype Typhimurium strains isolated from
infants with acute gastroenteritis. These strains were resistant to
-lactams, chloramphenicol, co-trimoxazole, and the most commonly
used aminoglycosides. The antibiotic resistance determinants of the
S. enterica serotype Typhimurium isolates were all
transferable, being carried by conjugative plasmids belonging to the
IncFI (R-ApCmKmSmSuTpTe) and IncL/M (R-ApKmSuGmAk) incompatibility groups.
We identified three different class 1 integrons which account for almost the entire resistance phenotype observed in Salmonella isolates; tetracycline and trimethoprim resistance is the only plasmid-encoded resistance not located within integrons. In-t1 (R-CmKmSu) and In-t2 (R-ApSmSu) were located on the IncFI plasmid in all isolates tested, while In-t3 (R-KmSuGmAk) was located on the IncL/M plasmid, which was carried by ca. 20% of the isolates. All these isolates were negative for class 2 and 3 integrons.
The presence in the same isolate of three class 1 integrons located on two different plasmids has, to our knowledge, never been observed. In addition, the repertoire of antibiotic resistance carried by In-t1, In-t2, and In-t3 represents one of the most extensive examples of gene cassette arrays thus far described among multi-drug-resistant isolates.
The role of integrons in the acquisition and spread of antibiotic resistance has not yet been fully investigated. Several studies have reported the presence of class 1 integrons in gram-negative bacteria from patients with hospital-acquired infections (i.e., Klebsiella pneumoniae, P. aeruginosa, E. coli, and Citrobacter freundii [20]) or in Klebsiella oxytoca strains responsible for nosocomial outbreaks (34). The integron-borne gene cassettes found in the S. enterica serotype Typhimurium isolates have previously been identified within class 1 integrons. The oxa-1 gene was found to be associated with aadA1a in transposon Tn2603 (32), and the aacA4-aacC1 association was reported for a K. oxytoca integron (34). The catB3 and aadB gene cassettes are located in the same class 1 integron in plasmid pBWH301 (2). Moreover, the aadA1a gene cassette, which we found in both In-t2 and In-t3, occurs at a high frequency in Tn21 derivatives (40) and has recently been described in multi-drug-resistant S. enterica serotype Typhimurium DT104 strains isolated from pig herds in Denmark (42).
Our data indicated that the integron-borne aadA1a gene cassette is silent in In-t3, while it is expressed when it is located in In-t2. This is likely due to the polarity effects observed for promoter-proximal and promoter-distal gene cassettes (39). In fact, the sequence determined for the Pant promoter of In-t3 has previously been reported to be 20-fold more active than those of the variants found in In-t1 and In-t2 (6).
The presence of In-t1 and In-t2 on the Salmonella IncFI plasmid leads to other interesting considerations. In fact, this plasmid has been implicated in the wide diffusion of multi-drug-resistant Salmonella strains. From 1969 to 1980, considerable clinical and epidemiological evidence indicated that the emergence and prevalence of some epidemic strains of human Salmonella spp. were correlated with the acquisition of conjugative or defective conjugative IncFI plasmids conferring resistance to multiple drugs and ranging in size from 100 to 180 kb. These plasmids were very common in different serotypes of Salmonella when the R type was R-ApCmKmSmSuTe or R-ApCmSmSuTe (1, 4, 37). The IncFI plasmid that we found in the recent isolates of S. enterica serotype Typhimurium has been compared with the prototypic pZM61 IncFI plasmid (R-ApCmKmTe) harbored by the epidemic strain S. enterica serotype Wien WZM6 isolated in Italy in 1974 (24). It is not known whether some ancestral IncFI plasmids harbored integrons, but our data clearly demonstrate that strain WZM6 does not contain integrons. Our observations suggest that the IncFI plasmids of Salmonella spp. could have evolved through the acquisition of integrons as genetic vehicles of the resistance genes. Several pieces of evidence indicate that the acquisition of integrons by R plasmids may have originated from the spread of Tn5090-like transposons (35). However, multiple site-specific recombination events occurring between the primary site attI and secondary sites can also lead to the fusion of the conserved integron sequences to plasmids and could represent a further mechanism for the acquisition of integrons (19). It will be interesting to determine whether the integrase site-specific recombination sites recently found in the E. coli F plasmid (12) are also present in the homologous Salmonella IncFI plasmid (28) and if these secondary sites have been involved in the acquisition of In-t1 and/or In-t2.
The presence of an additional integron, In-t3, in a limited number of isolates derives from the acquisition of a 100-kb IncL/M plasmid and results in an extended spectrum of resistance (resistance to gentamicin and amikacin). The presence in In-t3 of two putative open reading frames (X and X') endowed with no apparent function suggests that coding DNA modules other than antibiotic resistance genes can be packaged within integrons, providing a natural mechanism for the engineering of bacterial genomes (39).
Molecular models for the generation of new integron gene cassette
arrays require the simultaneous presence of different integrons in the
same cell (12, 14, 15, 26). The coexistence of two plasmids
carrying integrons with different gene cassettes is expected to result
in the transfer of cassettes from one plasmid to the other through the
intI1-dependent integrative and excisive model (25,
38). Furthermore, the coexistence of multiple integrons on the
same plasmid can frequently result in deletions of these elements
(15). Although both In-t1 and In-t2 appear to be very stable
on the IncFI plasmid, since they were identical in all prototypic
strains tested, future analysis of more recent Salmonella isolates might demonstrate gene cassette exchanges among In-t1, In-t2,
and In-t3. It should be pointed out that the IncL/M plasmid, which
contains In-t3, confers resistance to
-lactams through a still
unidentified beta-lactamase gene which was not found among integron-borne gene cassettes. The copy number of this plasmid is
higher than that of the IncFI plasmid, and this could result in an
enhancement of the antibiotic resistance levels due to an increased
gene dose. Under selective antibiotic pressure, these last two features
might have contributed to the stable maintenance of the entire IncL/M
plasmid rather than to the acquisition of a third integron by the
resident IncFI plasmid or the in trans integration of
additional gene cassettes within In-t1 and/or In-t2.
Although our findings strongly support the hypothesis that integron exchange represents a very efficient strategy for the acquisition of new antibiotic resistance genes, a prospective long-term observation of the natural evolution of the S. enterica serotype Typhimurium IncFI plasmids could provide further insight into the natural forces behind the acquisition and spread of integrons.
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ACKNOWLEDGMENTS |
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We are very grateful to Asmi Dibra of the Institute of Public Health of Tirana, Tirana, Albania, for his enthusiastic collaboration and for kindly providing the Salmonella strains. We thank Werner K. Maas for generously providing the inc and rep plamid bank. We also thank Antonio Cassone, Mauro Nicoletti, Annalisa Pantosti, and Alfredo Caprioli for critical review of the manuscript and Susanna Mariotti, Sergio Arena, Ildo Benedetti, and Teodoro Squatriti for excellent technical assistance.
This work was partially supported by the UNICEF project Control of Acute Diarrheal Diseases Including Cholera in Albania.
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FOOTNOTES |
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* Corresponding author. Mailing address: Laboratory of Bacteriology and Medical Mycology, Istituto Superiore di Sanità, V. le Regina Elena 299, 00161 Rome, Italy. Phone: 39-6-49903128. Fax: 39-6-49387112. E-mail: ALECARA{at}ISS.IT.
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