Macrolide-resistant Shigella sonnei.

Shigella sonnei UCN59, isolated during an outbreak of S. sonnei in January 2007, was resistant to azithromycin (MIC 64 mg/L). The isolate contained a plasmid-borne mph(A) gene encoding a macrolide 2'-phosphotransferase that inactivates macrolides. Emergence of the mph(A) gene in S. sonnei may limit usefulness of azithromycin for treatment of shigellosis.

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Shigellosis remains a common gastrointestinal disease in developing and industrialized countries. It occurs mostly in children <5 years of age; Shigella sonnei is the most frequently isolated species (1). Ampicillin and trimethoprim-sulfamethoxazole alleviate the dysenteric syndrome of shigellosis and reduce the infectious period. However, current resistance patterns limit the use of these drugs (2). Although fluoroquinolones are an effective alternative for adults, they are not approved for shigellosis treatment in children <18 years of age because of their potential toxicity (2,3). Azithromycin, a macrolide, represents an attractive treatment option for several reasons. It has in vitro activity against most Shigella spp. isolates (4), can be given once a day, and attains high intracellular concentrations (5). Despite MICs from 2 to 8 mg/L for Shigella spp., sufficient concentrations of azithromycin in the colon may inhibit Shigella spp. growth (6). Azithromycin is recommended by the American Academy of Pediatrics for treatment of shigellosis in children, by the World Health Organization as a second-line treatment in adults, and, since June 2004, by the Agence Francaise de Securite Sanitaire des Produits de Sante (2,7; www.agmed. sante.gouv.fr/htm/10/filcoprs/mp040601.pdf). In 1996, 2002, 2003, and 2007, outbreaks of shigellosis caused by S. sonnei resistant to ampicillin and trimethoprimsulfamethoxazole occurred in children in northern Paris. The outbreaks occurred in religious schools, similar to cyclic outbreaks in US Jewish schools related to secondary transmission (8,9).We report an outbreak of shigellosis in and around Paris, France, in which azithromycin failure was related to emergence of plasmid-mediated resistance to macrolides.

The Study

On January 24, 2007, S. sonnei strain UCN59 was isolated from a 4-year-old girl admitted to Robert Debre Hospital, Paris, for bloody diarrhea and fever. The strain was resistant to ampicillin, trimethoprim, sulfonamides, and cotrimoxazole but susceptible to quinolones, third-generation cephalosporins, and doxycycline according to the disk-diffusion technique. MICs of macrolides were markedly increased for S. sonnei UCN59 compared with those for a susceptible control S. sonnei UCN62 (Table). From January to April 23, 2007, a total of 50 cases of laboratory-confirmed shigellosis were identified. Isolates included, in addition to UCN59, 31 S. sonnei that had an azithromycin MIC [greater than or equal to]64 mg/L from 31 children <15 years of age, who had each been prescribed azithromycin for diarrhea. All patients lived in the Paris area and attended 8 religious schools.

Typing by pulsed-field gel electrophoresis (PFGE) and repetitive sequence-based PCR (rep-PCR) by using the automated DiversiLab system (bioMerieux, La-Balmeles-Grottes, France) (10) was performed on the 32 azithromycin-resistant and on 11 azithromycin-susceptible (MIC <16 mg/L) sporadic or outbreak isolates obtained during 1996-2007 in the Paris area. Five different PFGE patterns were obtained by using the enzyme BlnI. All the 2007 outbreak isolates, including the 32 azithromycin-resistant isolates and 2 azithromycin-susceptible isolates, were clustered into a single profile, profile 1 (Figure 1). The presence of azithromycin-susceptible isolates with profile 1 was detected among the 1996 and 2002-2006 outbreak isolates (data not shown), showing the persistence of this clonal type over 10 years in this area of Paris. Other isolates displayed PFGE types 2 to 5. Low diversity of PFGE profiles was consistent with isolation of strains in the same area and for most of them from the same community. Four different patterns with <97% similarity were distinguished by rep-PCR (Figure 2). Again, all the 2007 azithromycin-resistant isolates were clustered; however, they could be distinguished from the 2007 azithromycin-susceptible isolates. In contrast to PFGE findings, rep-PCR showed that isolates representative of the 1996, 2002, and 2003 outbreaks were genetically related.

The mph(A) gene, which encodes a macrolide 2'-phosphotransferase that inactivates macrolide antimicrobial drugs, was amplified from S. sonnei UCN59 DNA by PCR (11). PCR was negative for the erm(A), erm(TR), erm(B), erm(C), and erm(X) methylase genes; the ere(A), ere(B) genes encoding esterases; the mph(B) gene encoding a phosphotransferase; and the efflux genes mef(A) and msr(A). Sequence of the genes that encode ribosomal structures composing the target of macrolides, rrl, rplD, and rplV genes in S. sonnei UCN59, did not display any mutation in the critical bases of resistance to macrolides.

The genes conferring resistance to ampicillin and erythromycin were transferred en bloc by conjugation from S. sonnei UCN59 to a macrolide-susceptible mutant Escherichia coli AG100A at a frequency of [approximately equal to][10.sup.-3] per donor cell-forming unit after the mating period. A single plasmid was extracted from a transconjugant E. coli AG100A/pUV21. After restriction analysis, its size was estimated at [approximately equal to]90 kb. PCR experiments showed that this plasmid belonged to incompatibility group I (12). MICs of macrolides for E. coli AGI00A/pUV21 confirmed that this plasmid conferred cross-resistance to macrolides (Table).

EcoRI-restricted fragments of plasmid pUV21 were transferred to a nylon membrane and hybridized to an mph(A) probe. The mph(A) gene was borne by an [approximately equal to]20-kb EcoRI fragment, confirming that resistance to azithromycin was plasmid mediated.

After plasmid digestion with PstI enzyme, a DNA fragment that conferred resistance to erythromycin was cloned in plasmid pUC 18 and introduced by transformation into E. coli AG100A to generate E. coli K12 AG100A/ pUC18[ohms]mph(A). Sequence of the inserted DNA was determined. The fragment contained 4 open reading frames (ORFs) in the same orientation: mph(A), mrx that putatively encodes a membrane protein, mphR(A) that regulates the expression of mph(A), and an ORF of unknown function. This series of ORFs was flanked by a copy of IS26 at the 5' end and a copy of IS6100 at the 3' end. BLAST analysis (www.ncbi.nlm.nih.gov/blast/Blast.cgi) showed that the nucleotide sequence was nearly identical to that of fragments of plasmid pU302L from Salmonella enterica serotype Typhimurium (C.Y. Chen et al., unpub, data, GenBank accession no. NC_006816), of Shigellaflexneri transposon TnSF1 (J.H. Chen and J.Y. Chen, unpub, data, GenBank accession no. AF188331), and of plasmids pRSB101 and pSRB107 (13,14).

[FIGURE 1 OMITTED]

[FIGURE 2 OMITTED]

Conclusions

Few data are available on azithromycin resistance in Shigella spp. A recent report from Bangladesh mentioned that 16% of Shigella isolates were resistant to azithromycin and that 62% had intermediate resistance according to the Clinical Laboratory Standards Institute breakpoints recommended for streptococci ([greater than or equal to]1 mg/L, resistant; <0.25 mg/L, susceptible) (15). However, the [MIC.sub.90] (MIC at which 90% are susceptible) of 8 mg/L displayed by the microorganisms was within the normal range of MICs for this microorganism; no isolate had an azithromycin MIC >24 mg/L, which suggests that none had acquired resistance to azithromycin. Surveillance for resistance to azithromycin in Shigella spp. requires specific breakpoints for this species (3).

The mph(A) gene has been detected in the sequence of transposon TnSF1 isolated from S. flexneri (J.H. Chen and J.Y. Chert JY, unpub, data, GenBank accession no. AF188331). The mph(A) gene was first reported in an E. coli isolate from Japan (10). Since then, the gene has been found in Aeromonas hydrophila, Pseudomonas spp., Stenotrophomonas spp., and a variety of enterobacteria (listed at http://faculty.washington.edu/marilynr/ ermweb4.pdf).

Azithromycin was used to treat shigellosis in France only after the release of the French recommendations in 2004. Subsequent rapid emergence of azithromycm-resistant isolates may be a limitation for the use of macrolides in shigellosis. Because use of azithromycin is proposed for treatment of shigellosis, susceptibility of the isolates to azithromycin should be routinely tested.

References

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(2.) Centers for Disease Control and Prevention. Outbreaks of multi-drug-resistant Shigella sonnei gastroenteritis associated with day care centers--Kansas, Kentucky, and Missouri, 2005. MMWR Morb Mortal Wkly Rep. 2006;55:1068-71.

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(7.) World Health Organization. Guidelines for the control of shigellosis, including epidemics due to Shigella dysenteriae type 1 [cited 2008 Apt 1]. Available from http://whqlibdoc.who.int/ publications/2005/9241592330.pdf

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(9.) Sobel J, Cameron DN, ismail J, Strockbine N, Williams M, Diaz PS, et al. A prolonged outbreak of Shigella sonnei infections in traditionally observant Jewish communities in North America caused by a molecularly distinct bacterial subtype. J Infect Dis. 1998; 177:1405-9.

(10.) Healy M, Huong J, Bittner T, Lising M, Frye S. Microbial DNA typing by automated repetitive-sequence-based PCR. J Clin Microbiol. 2005;43:199-207. DOI: 10.1128/JCM.43.1.199-207.2005

(11.) Noguchi N, Emura A, Matsuyama H, O'Hara K, Sasatsu M, Kono M. Nucleotide sequence and characterization of erythromycin resistance determinant that encodes macrolide 2'-phosphotransferase I in Escherichia coli. Antimicrob Agents Chemother. 1995;39:2359-63.

(12.) Carattoli A, Bertini A, Villa L, Falbo V, Hopkins KL, Threlfall EJ. Identification of plasmids by PCR-based replicon typing. J Microbiol Methods. 2005;63:219-28. DOI: 10.1016/j.mimet.2005.03.018

(13.) Szczepanowski R, Krahn I, Linke B, Goesmann A, Puhler A, Schluter A. Antibiotic multiresistance plasmid pRSB101 isolated from a wastewater treatment plant is related to plasmids residing in phytopathogenic bacteria and carries eight different resistance determinants including a multidrug transport system. Microbiology. 2004;150:3613-30. DOI: 10.1099/mic.0.27317-0

(14.) Szczepanowski R, Braun S, Riedel V, Schneiker S, Krahn I, Puhler A, et al. The 120 592 bp IncF plasmid pRSB107 isolated from a sewage-treatment plant encodes nine different antibiotic-resistance determinants, two iron-acquisition systems and other putative virulence-associated functions. Microbiology. 2005;151:1095-111. DOI: 10.1099/mic.0.27773-0

(15.) Rahman M, Shoma S, Rashid H, El Arifeen S, Baqui AH, Siddique AK, et al. Increasing spectrum in antimicrobial resistance of Shigella isolates in Bangladesh: resistance to azithromycin and ceftriaxone and decreased susceptibility to ciprofloxacin. J Health Popul Nutr. 2007;25:158-67.

Leyla Boumghar-Bourtchai, * Patricia Mariani-Kurkdjian, ([dagger]) Edouard Bingen, ([dagger]) Ingrid Filliol, ([double dagger]) Anne Dhalluin, * ([section]) Shadia Ait Ifrane, ([dagger]) Francois-Xavier Weill, ([double dagger]) and Roland Leclercq *

* Centre Hospitalier Universitaire Cote de Nacre, Caen, France; ([dagger]) Hopital Robert Debre, Paris, France; ([double dagger]) Institut Pasteur, Paris; and ([section]) Universite de Caen, Caen

DOI: 10.3201/eid1408.080147

Dr Boumghar-Bourtchai is pursuing a PhD degree at the University of Caen; she completed this work as part of her PhD program. Her main research interest is emergence of unusual mechanisms of resistance to macrolides in various bacteria, such as S. sonnei, Turicella otitidis, and other gram-positive organisms.

Address for correspondence: Roland Leclercq, CHU de Caen, Service de Microbiologie, avenue Cote de Nacre, 14033 Caen CEDEX, France; email: [e-mail]

Use of trade names is for identification only and does not imply endorsement by the Public Health Service or by the U.S. Department of Health and Human Services.

Table. Macrolide susceptibility of outbreak and control Shigella
isolates and Escherichia coli constructs

                                                    MIC, mg/L

Strain                                   Erythromycin   Clarithromycin

Shigella sonnei UCN 62                        64              32
S. sonnei UCN 59                            1,024           1,024
Escherichia coli K12 AG100A                   2               2
E. coli K12 AG100A/pUV21                     512             512
E. coli K12 AG100A/pUC18[OMEGA]mph(A)       1,024            512

                                                    MIC, mg/L

Strain                                   Azithromycin   Telithromycin

Shigella sonnei UCN 62                        2               8
S. sonnei UCN 59                              64              64
Escherichia coli K12 AG100A                   2               1
E. coli K12 AG100A/pUV21                      8               32
E. coli K12 AG100A/pUC18[OMEGA]mph(A)        128             512