CITATION: Roy PH. 1995. Integrons: novel mobile genetic elements mediating antibiotc resistance in enterobacteria and Pseudomonas. APUA Newsletter 13(3):1, 4-6.


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Integrons: novel mobile genetic elements mediating antibiotic resistance in Enterobacteria and Pseudomonas
Paul H Roy
Université Laval, Ste Foy, Québec, Canada

The problem of multiple antibiotic resistance in Gram-negative bacteria has been somewhat overshadowed recently by the more acute problem of resistant Gram-positive bacteria, including vancomycin-resistant enterococci (VRE) and methicillin-resistant Staphylococcus aureus (MRSA). However, aided by some intricate genetic mechanisms, Gram-negative bacteria have been slowly but steadily accumulating and disseminating multiple resistance to widely used antibiotics to a point where, particularly for Pseudomonas, therapeutic choices are becoming very limited.

Plasmids, transposons, and integrons
Many resistance genes in
Enterobacteriaceae and Pseudomonas are on large, transferable extrachromosomal DNA elements, called plasmids, on which may be other mobile elements, called transposons. Some transposons code for single resistances, e.g., the TEM beta-lactamase (and all of its extended spectrum derivatives) on Tn3, kanamycin resistance on Tn5, and tetracycline resistance on Tn10. Plasmids and transposons coding multiple drug resistance often possess another genetic element, the more recently described integron (Figure 1).

Integrons contain one, or more, antibiotic resistance gene which is present as a mobile gene cassette, inserted in various arrangements between two conserved DNA regions (Figure 1 +2). Integrons were discovered in the mid-1980's, when DNA sequencing of several resistance genes revealed a common sequence in their upstream region (1-4). The upstream region codes for a common promoter for the inserted antibiotic resistance genes and, on the opposite strand, an integrase similar to those of temperate bacteriophages (5). The integrase has been shown to mediate gene cassette excision and insertion via circular intermediates (6,7) (Figure 1). Thus, cassettes are in fact mobile elements, although they do not code for genes involved in their own mobility. Their movement is allied to the integrase activity.

An interesting feature of cassettes is a palindromic sequence known as a 59-base element which occurs at the end of the cassette. The 59-base elements are involved in the site-specific recombination reaction and differ among cassettes, although they have similar DNA sequences at their extremities (8). Cassettes insert preferentially up front in the integron, immediately downstream of the promoter region, which produces the highest expression. Further away from the promoter region, expression is decreased (9). As cassettes "leap-frog", antibiotic selection pressure can select cassette arrangements in which a given resistance is nearest the promoter and thus most strongly expressed. In addition to the mobility of cassettes, whole integrons are also mobile elements. At least one integron, Tn
402, has a complete set of four transposition genes (10).

Evolution of integrons
Integrons probably were around for a long time, evolutionarily speaking, before ever having seen an antibiotic resistance gene. The ancestral integron comes from an organism, not necessarily related to clinical bacteria, with a moderately G+C rich DNA. An "empty" integron has been found on plasmid pVS1 (11). In the plasmid, the conserved regions are immediately adjacent, confirming that 59-base elements are associated with the resistance gene cassettes themselves (Figure 2). However, no free 59-base elements, and no resistance genes identical to those found in integrons, have yet been found in the DNA database. It remains unknown how resistance genes become associated with 59-base elements and how they are recruited into integrons. Codon usage analysis indicates a wide variety of origins of the genes found as cassettes.

The first cassette to arrive in integrons may have been the
qacE antiseptic resistance gene (see Tn402, Figure 2a). Most integrons are descended from a version in which the qacE gene has been truncated by the non-specific insertion of a sulfonamide resistance gene and in which two of the transposition genes have been lost. Thus, most integrons are defective transposons. It is interesting to speculate whether the arrival of the qacE cassette dates from the 1920's, when acridine orange was used therapeutically and the insertion of the sulfonamide gene from the 1930's. In contrast, codon usage analysis indicates a close correlation between, and thus a potentially long-co-evolution of, the integrase and the transposition genes. There may have been an ancient association between a transposon and the remnants of a temperate phage.

A second class of integrons occurs in the transposon Tn
7 and its relatives (Figure 2b). Only a very limited range of cassettes are found, including resistance to trimethoprim (dhfrI), streptothricin (sat) and streptomycin-spectinomycin (aadA1) (12). The dhfrI and aadA1 cassettes are identical to those found in the pVS1 class of integrons. Indeed the dhfrI cassette may have first occurred in Tn7, later being transferred into the pVS1 class of integrons where, in plasmid pLMO150 (13), dhfrI is now associated with sulfonamide resistance, thus limiting the usefulness of the low-cost antibiotic co-trimoxazole. It is worthy of note that these two plasmids were isolated from strains of Shigella from Sri Lanka.

Resistance genes within integrons
Integron-borne genes include beta-lactamases (OXA, PSE, and CARB), aminoglycoside modifying enzymes (
aacA4, aacC1, aadB, and many others), trimethoprim resistance (dhfr's I, IIa, IIb, IIc, V, VII, IX, X, and XII) and chloramphenicol resistance (cmlA and cat, see below). Clinically the most important up to now have been the amikacin (aacA4) and gentamicin (aacC1, aadB) resistance genes.

The mapping and sequencing of integrons has led to the characterization of some novel mechanisms of resistance. The
cmlA gene of Tn1696, which expresses non-enzymatic chloramphenicol resistance, codes for an integral membrane protein, likely an efflux protein (14). The chloramphenicol acetyltransferase (Cat) of Tn2424 was, surprisingly, dissimilar to the known Cat's (which all were similar to one another) and rather resembled another acetyltransferase family (15). However, several Cat's of the new type have now been found, both in integrons and elsewhere.

Carbapenem resistance on an integron
Recently a novel type B beta-lactamase, which inactivates imipenem and related carbapenems, has been located on an integron. Its emergence poses a threat for rapid dissemination both geographically and among species. The IMP-1 carbapenemase was first described as a chromosomal gene in
Serratia marcescens strain TN9106 (16). The sequence upstream of the structural gene is the conserved sequence of an integron, although this fact was not mentioned by the authors at that time. An identical IMP-1 gene, also just downstream of the integron conserved sequence, was found in plasmid RDK4 in Klebsiella aerogenes (17).

Again the identical IMP-1 gene has been cloned from another
S. marcescens strain, AKL9373 (18). Unlike S. marcescens TN9106, IMP-1 is plasmid encoded in AK9373. In the upstream sequence in AK9373 is a gene which codes for yet another integrase! Its closest relatives are the pVS1 integrase (60% identity) and the Tn7 integrase (45% identity). Moreover, at its downstream end the IMP-1 cassette is followed by an aacA4 (aminoglycoside-6'-acetyltransferase) cassette. Thus it appears that this is the first example of a third class of integrons.

The pVS1-class integrons, the Tn
7-class integrons, and the new integron recently isolated in Serratia may thus represent transposons which long ago obtained integrases and attachment sites from cryptic prophages, and have fortuitously become ideal vehicles for dissemination of genes which enable survival under strong selective pressure. Thus far they harbor antibiotic resistance genes, although open reading frames (orf's) for proteins of unknown function suggest that integrons serve other purposes in cell survival. How chromosomal genes acquire 59-base elements and become cassettes and whether other genes, such as virulence factors, have the potential to become cassettes remains unknown for the present.

References

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  16. Osane E, Arakawa Y. Wacharotayankun R, Ohta M, Horii T, Ito H, Yosihimura F, Kato N. Antimicrob Agents Chemother 1994; 38:71-78.
  17. Sawai T. GenBank submission, accession number D29636.
  18. Arakawa Y, Murakami M. Suzuki K, Ito H, Wacharotayankum R, Ohsuka S, Kato N, Ohta M. Antimicrob Agents Chemother 1995; 39:1612-1615.
 

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