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Antimicrobial Agents and Chemotherapy, September 2002, p. 3054-3056, Vol. 46, No. 9
0066-4804/02/$04.00+0     DOI: 10.1128/AAC.46.9.3054-3056.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Clinical Isolates of Staphylococcus aureus with Ribosomal Mutations Conferring Resistance to Macrolides

Anne-Laure Prunier,1 Brigitte Malbruny,1 Didier Tandé,2 Bertrand Picard,2 and Roland Leclercq1*

Service de Microbiologie, CHU Côte de Nacre, Caen,1 Service de Microbiologie, CHU Morvan, Brest, France2

Received 4 March 2002/ Returned for modification 1 May 2002/ Accepted 3 June 2002


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ABSTRACT
 
Six strains of Staphylococcus aureus isolated from cystic fibrosis patients after treatment with azithromycin were cross-resistant to azithromycin and erythromycin. None of the isolates contained erm or msr(A) genes, but they all carried either A2058G/U or A2059G mutations within the rrl genes, with a majority of the rRNA copies bearing the mutation. One strain displayed an additional mutation in the rplV gene, encoding the L22 ribosomal protein.


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TEXT
 
Emergence of resistance to macrolides in staphylococci shortly after the therapeutic use of erythromycin has been reported (3). In most cases, macrolide resistance in clinical isolates of staphylococci has been linked to target site alteration due to methylation of adenosine 2058 (A2058) of 23S rRNA within the large ribosomal subunit (8). These ribosomal methylases are encoded by erm genes. In some cases, ABC transporters encoded by plasmid-borne msr(A) genes cause active efflux of 14-member-ring (erythromycin, clarithromycin, roxithromycin, and dirithromycin) or 15-member-ring (azithromycin) macrolides (14). Rare staphylococcal strains have been reported to produce a macrolide phosphotransferase which inactivates some of these antimicrobials (12, 20). Overall, in several survey studies, drug efflux and ribosomal methylation have been found to be responsible for macrolide resistance in all of the strains studied (10, 15).

The use of macrolides for the treatment of staphylococcal infections is generally limited to uncomplicated soft tissue infections. Recently, it has been inferred from anti-inflammatory and antiadhesion effects of macrolides observed in vitro that these antimicrobials may have a favorable action at low concentrations for treatment of Pseudomonas aeruginosa infections (7). These indirect effects might be helpful in the case of cystic fibrosis, where the major cause of morbidity and mortality remains respiratory disease, with P. aeruginosa as the most frequently organism isolated, followed by Staphylococcus aureus (5). We report on six strains of erythromycin-resistant S. aureus, isolated from patients suffering from cystic fibrosis, with unusual mutations of the ribosomal target of macrolides.

Bacterial strains and antimicrobial susceptibility testing. Among 12 S. aureus strains resistant to erythromycin and isolated from cystic fibrosis patients, 6 did not contain erm or msr(A) genes as determined by PCR (1). These strains, S. aureus UCN13, UCN14, UCN15, UCN16, UCN17, and UCN18, were isolated at the hospitals of Brest and Caen, France, from the sputa of five patients (S. aureus UCN13 and UCN14 were isolated from the same patient) suffering from cystic fibrosis who were treated with azithromycin (10 mg/kg/day) for a minimum of 3 months and a maximum of 1 year. The strains were considered to be genetically unrelated since the patterns of SmaI-restricted DNA differed by more than three fragments after pulsed-field gel electrophoresis analysis (data not shown) (18). All isolates were resistant to erythromycin as determined by the disk diffusion technique. Macrolide-susceptible S. aureus ATCC 29213 was included as a control. MICs of antibiotics were determined by the agar dilution method with Mueller-Hinton medium. Dalfopristin (RP54476), erythromycin, quinupristin (RP57669), quinupristin-dalfopristin, pristinamycin, and spiramycin were from Aventis Pharma (Romainville, France), and lincomycin was from Pharmacia-Upjohn (Kalamazoo, Mich.).

PCR and DNA sequence analysis. As mentioned above, no rRNA methylase genes [erm(A), erm(B), and erm(C)] or efflux gene [msr(A)] could be detected by PCR with specific primers (1). Since mutations in genes coding for L4 or L22 ribosomal proteins or in domains II and V of 23S rRNA have been reported to be responsible for macrolide resistance in a variety of bacterial species, we hypothesized that similar mutations might account for resistance in the strains studied (2, 16, 19). Portions of rrl genes for domains II and V of 23S rRNA and the genes for ribosomal proteins L4 and L22 were amplified by PCR from total genomic DNA with the oligonucleotides shown in Table 1. The amplification primers were designed after analysis of the sequence of S. aureus COL obtained from The Institute for Genomic Research website (http://www.tigr.org). Mutations were screened for by PCR-SSCP, as described previously (2). After heat denaturation, the single-stranded PCR products were separated by nondenaturing polyacrylamide gel electrophoresis. Fragments with mobilities different from those of susceptible controls were sequenced.


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  		TABLE 1. Oligodeoxynucleotides used for the amplification of fragments of the 23S rRNA gene and of ribosomal protein genes

We also determined the copy numbers of the rrl genes carrying 23S rRNA mutations. A strategy was developed to amplify the different copies of rrl domain V individually. Sequence analysis of S. aureus COL showed that the strain carried six copies of the rrl gene. We used primers complementary to unique sequences downstream from each rrl gene (V LA to V LF in Table 1) and a primer common to the six alleles and complementary to a region upstream from the peptidyl transferase region in domain V (V U1). Internal primers (V U2 and V L2) were then used to amplify a 144-bp fragment encompassing the domain V region, which was subsequently sequenced.

Susceptibility to antimicrobials. The six isolates were highly resistant to erythromycin and azithromycin (MIC of >128 µg/ml) (Table 2). Five strains were also resistant to the 16-member-ring macrolide spiramycin, whereas the spiramycin MIC for strain UCN16 was lower (8 µg/ml). MICs of quinupristin, a streptogramin B, and clindamycin were more widely distributed. MICs of dalfopristin, a streptogramin A, were similar to those for susceptible strains (9). All strains except strain UCN15 were susceptible to quinupristin-dalfopristin and pristinamycin.


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  		TABLE 2. MICs of macrolides, lincosamides, and streptogramins

Identification of ribosomal mutations. Sequencing showed that SSCP mobilities of fragments different from those of the controls amplified from S. aureus ATCC 29213 were associated with point mutations or a deletion. Four strains, S. aureus UCN13, UCN15, UCN16, and UCN17, carried an A2058G (E. coli numbering) transition; S. aureus UCN14 contained an A2058T transversion; and S. aureus UCN18 had an A2059G transition. No mutation was detected in domain II of 23S rRNA or in the rplD gene (encoding the L4 protein). In strain UCN15, a deletion of nine nucleotides which would result in the deletion of three amino acids at position 101 of the deduced amino acid sequence of protein L22 was associated with the A2058G mutation. Mutations at positions A2058 and A2059 were associated with macrolide-lincosamide-streptogramin B and macrolide-lincosamide phenotypes, respectively, similar to those already reported for other organisms (19). Relative to other rRNA mutations, A2058G gives the highest level of resistance to 14-member-ring macrolides and confers macrolide-lincosamide-streptogramin B resistance, defined as high resistance to all of the antimicrobials in this group. However, MICs of clindamycin and quinupristin were lower than expected for strains UCN14, UCN15, UCN16, and UCN18. This might be due to the fact that these staphylococci grew slowly on agar, as has been reported for most S. aureus strains isolated from cystic fibrosis patients, which frequently yield small-colony variants (6). The A-to-U or A-to-G substitutions gave a similar level of resistance. The A2059 mutation gave the macrolide-lincosamide phenotype, with moderate resistance to clindamycin and no resistance to streptogramins B, as previously reported for Helicobacter pylori and Streptococcus pneumoniae (17, 19).

Resistance by mutation in 23S rRNA has generally been reported for bacteria with few copies of rrn operons, such as H. pylori, Mycoplasma pneumoniae, Mycobacterium intracellulare, and Mycobacterium avium. However, mutations in 23S rRNA have been reported for S. pneumoniae, which contains four rrn operons (2, 4, 16). In PCR experiments carried out to determine the copy numbers of mutated rrl genes, one copy, named B, could not be amplified from five of our strains (Table 3). In silico analysis of strain N315 DNA, available at the National Center for Biotechnology Information website (http://www.ncbi.nlm.nih.gov), revealed that it also contained only five rrl copies and that the copy at a position similar to that of the B copy was missing. In every erythromycin-resistant strain, three or four copies were mutated, confirming that mutation in a majority of rrl operons was associated with significant resistance, as reported for S. pneumoniae (Table 3).


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  		TABLE 3. Mutations of the rrl genes

Resistance to streptogramins was observed in strain UCN15, which combined a rplV mutation with an A2058G mutation. Recently, resistance to quinupristin-dalfopristin in staphylococcal strains selected under treatment with this antibiotic has been explained by similar mutations in the conserved 3' end of the rplV gene (11)).

Isolation of staphylococci with resistance to macrolides conferred by ribosomal mutations is unusual. It may be related to the specific context of cystic fibrosis. Half of 12 erythromycin-resistant strains of S. aureus isolated from cystic fibrosis patients in our institutions were mutants. Indeed, patients suffering from this genetic disorder receive multiple courses of antibiotics. In addition, administration of macrolides at low doses aimed at preventing Pseudomonas infections might favor the emergence of mutants, although no definitive relationship could be proven in this study. Finally, colonization of cystic fibrosis patients by hypermutable strains of P. aeruginosa has been reported (13). A similar possibility for the staphylococcal isolates is currently under investigation.


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ACKNOWLEDGMENTS
 
This work was supported in part by a grant from the association Vaincre la Mucoviscidose.


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FOOTNOTES
 
* Corresponding author. Mailing address: CHU de Caen, Service de Microbiologie, Avenue Côte de Nacre, 14033 Caen Cedex, France. Phone: (33) 02 31 06 45 72. Fax: (33) 02 31 06 45 73. E-mail: leclercq-r{at}chu-caen.fr. Back


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Antimicrobial Agents and Chemotherapy, September 2002, p. 3054-3056, Vol. 46, No. 9
0066-4804/02/$04.00+0     DOI: 10.1128/AAC.46.9.3054-3056.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.



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