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Antimicrobial Agents and Chemotherapy, November 2005, p. 4775-4777, Vol. 49, No. 11
0066-4804/05/$08.00+0 doi:10.1128/AAC.49.11.4775-4777.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Dipartimento di Genetica e Microbiologia,1 Dipartimento di Scienze Morfologiche, Eidologiche e Cliniche, University of Pavia, Pavia, Italy2
Received 23 June 2005/ Returned for modification 21 July 2005/ Accepted 12 August 2005
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Bacterial drug efflux pumps have been classified into five families (11). The genome of M. tuberculosis contains genes encoding drug efflux transporters from all of these families (http://www.membranetransport.org), and, as described in a recent review, several mycobacterial drug efflux pumps have been identified and characterized experimentally (8).
Resistance nodulation division (RND) transporters have been found in all major kingdoms of living organisms, but they seem to be involved in drug efflux only in gram-negative bacteria. The AcrAB/TolC drug efflux pump of Escherichia coli provides a prototype for such export systems, with AcrB constituting the membrane pump itself, AcrA the membrane fusion protein, and TolC the outer membrane component (12).
Interestingly, the genome sequence of M. tuberculosis revealed the presence of 13 putative transmembrane proteins, predicted to be transport proteins of the RND superfamily (5). Since these proteins appear to be confined to mycobacteria, they have been designated MmpL (mycobacterial membrane proteins, large). The hydrophobic nature of the MmpL proteins and the close association of four of their genes with those involved in lipid metabolism suggest that they may be naturally involved in the transport of fatty acids (13). Indeed, MmpL8 is involved in sulfolipid-1 biosynthesis by transporting a precursor of this molecule (6, 9), while the MmpL7 protein catalyzes the export of phthiocerol dimycocerosate (PDIM) in M. tuberculosis (3). A mutant lacking the mmpL7 gene was severely attenuated for growth in the lungs (7).
Given the similarities with other RND transporters, it is possible that the MmpL proteins can also act in drug efflux.
In this paper, we demonstrate that the mmpL7 gene from M. tuberculosis confers a high level of resistance to isoniazid (INH) when overexpressed in Mycobacterium smegmatis. The resistance level significantly decreases in the presence of efflux inhibitors. We also observed energy-dependent efflux of INH from M. smegmatis cells expressing the mmpL7 gene.
Transformation of the M. tuberculosis cosmid library into M. smegmatis and selection for INH resistance. A cosmid library of M. tuberculosis H37Rv constructed in the pYUB18 cosmid (kindly provided by S. Cole) was electroporated into M. smegmatis mc2155, and the transformants were selected on Middlebrook 7H11 agar supplemented with 10% (vol/vol) Middlebrook oleic acid-albumin-dextrose-catalase enrichment and 0.2% (vol/vol) glycerol containing different concentrations of INH. Three clones showed a high level of INH resistance (512 µg/ml, 16 times the MIC), while one clone had a moderate resistance (128 µg/ml, 4 times the MIC). Partial DNA sequence analyses revealed that all the cosmids responsible for a high INH resistance contained the inhA gene (1) and were discarded. The INH16 cosmid clone with moderate INH resistance was chosen for further characterization. The DNA fragment contained in this cosmid extends from nucleotides 3277340 to 3311634 of the M. tuberculosis genome and contains several genes, including mmpL7, on which we focused our attention. MmpL7, a protein of 920 amino acids with a predicted molecular mass of 95.1 kDa, contains 12 transmembrane domains (TMDs) and two large hydrophilic extracytoplasmic domains between TMD 1 and TMD 2 and between TMD 7 and TMD 8. All of these characteristics are described as typical of RND efflux pumps (14). Pairwise alignment of amino acid sequences showed that MmpL7 is 14% identical to and 46% similar to AcrB of E. coli (8).
mmpL7 gene overexpression is responsible for increased INH MIC of M. smegmatis. One way to validate the hypothesis that a gene protects against the toxic effects of a drug is to determine whether constitutive overexpression of the gene results in increased resistance to this drug. Consequently, to understand whether the INH resistance of M. smegmatis was conferred by the mmpL7 gene, the gene was amplified from INH16 cosmid DNA by PCR by using the 5'-TGAAGCTTATGCCTAGTCCGG-3' sense primer and the 5'-ATAAGCTTCGTGGCATGGGGTCT-3' antisense primer. The PCR product was cloned into pGEM-T Easy vector and sequenced on both strands. The mmpL7 gene was then cloned into pSODIT-2 shuttle expression vector containing the determinant of hygromycin resistance (kindly provided by D. Young). pSODIT-2 and pSODIT/mmpL7 plasmids were introduced into M. smegmatis mc2155 cells plated onto Middlebrook 7H11 agar containing hygromycin and INH concentrations ranging from 32 µg/ml to 512 µg/ml. The isoniazid resistance level shown by M. smegmatis cells expressing the mmpL7 gene was very high, more than 16 times the wild-type MIC (>512 µg/ml versus 32 µg/ml). Susceptibilities to ethambutol, ciprofloxacin, ofloxacin, tetracycline, rifampin, ethidium bromide, doxorubicin, and tetraphenylphosphonium were not affected (data not shown). Consequently, the mmpL7 gene seems to be responsible for the INH resistance.
The MIC of ethionamide, a structural analog of INH and a useful second-line antituberculosis drug, was also determined. The overexpression of the MmpL7 protein caused a fourfold increase in the MIC of ethionamide for M. smegmatis cells expressing the mmpL7 gene compared to the MIC for M. smegmatis cells containing the vector pSODIT-2 alone (100 µg/ml versus 25 µg/ml).
The INH MIC was also determined in the presence of the efflux inhibitors reserpine (12 µg/ml), CCCP (carbonyl cyanide m-chlorophenylhydrazone; 15 µg/ml), and verapamil (40 µg/ml) in order to evaluate the effects of different, well-known efflux pump inhibitors on resistance levels. M. smegmatis cells containing the recombinant plasmid pSODIT/mmpL7 and the pSODIT-2 expression vector were grown on the same medium used for MIC testing containing different isoniazid concentrations and the inhibitors described above. As shown in Fig. 1, reserpine and CCCP reduced the isoniazid resistance eightfold (512 µg/ml versus 64 µg/ml) in M. smegmatis cells carrying the plasmid pSODIT/mmpL7, while verapamil had no effect on isoniazid resistance. The decrease in the INH MIC is presumably due to the inhibition of drug efflux mediating by the mmpL7 gene product. On the contrary, the INH MIC of M. smegmatis cells carrying the vector pSODIT-2 was not affected by any of the tested inhibitors (Fig. 1).
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To test if the available source of energy could lead to drug efflux, 0.2% (vol/vol) glycerol was added 15 min after the addition of reserpine. As shown in Fig. 2B, M. smegmatis cells expressing the mmpL7 gene, treated with reserpine and glycerol, rapidly eliminated INH, whereas the cells treated with reserpine only did not extrude significant amounts of the drug. On the contrary, the addition of glycerol had no effect on the level of INH accumulation in the case of M. smegmatis cells, carrying the pSODIT-2 vector, which were treated with reserpine (data not shown).
Together, these results strongly indicate that the MmpL7 protein actively pumps out isoniazid in M. smegmatis. To our knowledge, MmpL7 is the first example of an RND-like transporter responsible for isoniazid resistance in M. smegmatis.
In order to begin to understand the range of efflux substrates for the MmpL proteins and to assess any potential role in drug resistance in M. tuberculosis, Domenech et al. (10) constructed mutant strains with 11 out of 13 of the mmpL genes inactivated. Since the drug susceptibilities of these mutants to a broad spectrum of agents are unaltered, the authors suggest that, unlike their function in other organisms, these proteins do not play a significant role in the intrinsic drug resistance of M. tuberculosis. It is noteworthy that the mmpL7 knockout in M. tuberculosis seems to have no effect on INH MICs. This only appears to be in contrast with our results, since in M. smegmatis the environmental conditions could be completely different. A search of the available M. smegmatis genome database revealed that the MmpL7 protein is not present in this organism, and this finding is in agreement with the statement that the PDIM molecule was not found in M. smegmatis (3). Consequently, the M. tuberculosis MmpL7 protein can utilize INH as a substrate when it is expressed in M. smegmatis, while in M. tuberculosis INH could compete with the natural substrate (PDIM) of MmpL7 since its principal physiological role appears to be the export of complex lipids to the cell exterior. However, we cannot exclude the possitibility that an overexpression of the mmpL7 gene in M. tuberculosis could be responsible for the low-level INH resistance in those clinical isolates for which no mutation in the known gene targets has been identified. Analysis of mmpL7 gene expression in these strains could confirm its role in low-level INH resistance.
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ACKNOWLEDGMENTS |
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We thank S. T. Cole for kindly providing the M. tuberculosis cosmid library and D. Young for pSODIT-2 vector.
M. R. Pasca and P. Guglierame contributed equally to the work.
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, addition of reserpine) or pSODIT-2 expression vector (
, no reserpine addition; 
, addition of reserpine). (B) Effect of the addition of reserpine and glycerol on the accumulation and efflux of isoniazid by M. smegmatis cells carrying the pSODIT/mmpL7 plasmid (•, no reserpine addition;