Loss of erythromycin resistance genes from strains of Streptococcus pyogenes that have developed resistance to levofloxacin

2009 ◽  
Vol 64 (2) ◽  
pp. 225-228 ◽  
Author(s):  
Dewan Sakhawat Billal ◽  
Muneki Hotomi ◽  
Steve S. Yan ◽  
Daniel P. Fedorko ◽  
Jun Shimada ◽  
...  
1998 ◽  
Vol 42 (2) ◽  
pp. 257-262 ◽  
Author(s):  
Helena Seppälä ◽  
Mikael Skurnik ◽  
Hanna Soini ◽  
Marilyn C. Roberts ◽  
Pentti Huovinen

ABSTRACT Erythromycin resistance among streptococci is commonly due to target site modification by an rRNA-methylating enzyme, which results in coresistance to macrolide, lincosamide, and streptogramin B antibiotics (MLSB resistance). Genes belonging to theermAM (ermB) gene class are the only erythromycin resistance methylase (erm) genes inStreptococcus pyogenes with MLSB resistance that have been sequenced so far. We identified a novelerm gene, designated ermTR, from an erythromycin-resistant clinical strain of S. pyogenes(strain A200) with an inducible type of MLSBresistance. The nucleotide sequence of ermTR is 82.5% identical to ermA, previously found, for example, in Staphylococcus aureus and coagulase-negative staphylococci. Our finding provides the first sequence of anerm gene other than ermAM that mediates MLSB resistance in S. pyogenes.


2011 ◽  
Vol 55 (7) ◽  
pp. 3226-3230 ◽  
Author(s):  
Maria Del Grosso ◽  
Romina Camilli ◽  
Giada Barbabella ◽  
John Blackman Northwood ◽  
David J. Farrell ◽  
...  

ABSTRACTInStreptococcus pyogenes, efflux-mediated erythromycin resistance is associated with themefgene, represented mostly bymef(A), although a small portion of strains carry differentmefsubclasses. We characterized the composite genetic elements, includingmefsubclasses other thanmef(A), associated with other resistance genes inS. pyogenesisolates. Determination of the genetic elements was performed by PCR mapping. The strains carrying mosaicmef(A/E), in which the 5′ region was identical tomef(A) and the 3′ region was identical tomef(E), also carriedtet(O). The two genes were found enclosed in an element similar toS. pyogenesprophage Φm46.1, designated the Φm46.1-like element. InS. pyogenesstrains carryingmef(E) andtet(M),mef(E) was included in a typical mega element, and in some strains, it was physically associated withtet(M) in the composite element Tn2009.S. pyogenesstrains carryingmef(I) also carriedcatQ; the two genes were linked in a fragment representing a portion of the 5216IQ complex ofStreptococcus pneumoniae, designated the defective IQ element. In the only isolate carrying a novelmefgene, this was associated withcatQandtet(M) in a genetic element similar to the 5216IQ complex ofS. pneumoniae(5216IQ-like complex), suggesting that the novelmefis in fact a variant ofmef(I). This study demonstrates that the composite elements containingmefare shared betweenS. pyogenesandS. pneumoniaeand suggests that it is important to distinguish themefsubclass on the basis of the genetic element containing it.


1999 ◽  
Vol 43 (1) ◽  
pp. 48-52 ◽  
Author(s):  
Janne Kataja ◽  
Pentti Huovinen ◽  
Mikael Skurnik ◽  
Helena Seppälä ◽  

Streptococcus pyogenes isolates (group A streptococcus) of different erythromycin resistance phenotypes were collected from all over Finland in 1994 and 1995 and studied; they were evaluated for their susceptibilities to 14 antimicrobial agents (396 isolates) and the presence of different erythromycin resistance genes (45 isolates). The erythromycin-resistant isolates with the macrolide-resistant but lincosamide- and streptogramin B-susceptible phenotype (M phenotype) were further studied for their plasmid contents and the transferability of resistance genes. Resistance to antimicrobial agents other than macrolides, clindamycin, tetracycline, and chloramphenicol was not found. When compared to our previous study performed in 1990, the rate of resistance to tetracycline increased from 10 to 93% among isolates with the inducible resistance (IR) phenotype of macrolide, lincosamide, and streptogramin B (MLSB) resistance. Tetracycline resistance was also found among 75% of the MLSB-resistant isolates with the constitutive resistance (CR) phenotype. Resistance to chloramphenicol was found for the first time in S. pyogenes in Finland; 3% of the isolates with the IR phenotype were resistant. All the chloramphenicol-resistant isolates were also resistant to tetracycline. Detection of erythromycin resistance genes by PCR indicated that, with the exception of one isolate with the CR phenotype, all M-phenotype isolates had the macrolide efflux (mefA) gene and all the MLSB-resistant isolates had the erythromycin resistance methylase (ermTR) gene; the isolate with the CR phenotype contained the ermB gene. No plasmid DNA could be isolated from the M-phenotype isolates, but the mefA gene was transferred by conjugation.


QJM ◽  
2018 ◽  
Vol 111 (suppl_1) ◽  
Author(s):  
M Abdel-Baseer Tohamy ◽  
M Abdelwahaab Abdelmeseeh ◽  
M S Sheemy ◽  
D Sabry Abdelfatah ◽  
M Ahmed Abdel Tawab

2014 ◽  
Vol 69 (6) ◽  
pp. 1474-1482 ◽  
Author(s):  
M. Montes ◽  
E. Tamayo ◽  
C. Mojica ◽  
J. M. Garcia-Arenzana ◽  
O. Esnal ◽  
...  

2003 ◽  
Vol 47 (9) ◽  
pp. 2844-2849 ◽  
Author(s):  
Eleonora Giovanetti ◽  
Andrea Brenciani ◽  
Remo Lupidi ◽  
Marilyn C. Roberts ◽  
Pietro E. Varaldo

ABSTRACT Sixty-three recent Italian clinical isolates of Streptococcus pyogenes resistant to both erythromycin (MICs ≥ 1 μg/ml) and tetracycline (MICs ≥ 8 μg/ml) were genotyped for macrolide and tetracycline resistance genes. We found 19 isolates carrying the mef(A) and the tet(O) genes; 25 isolates carrying the erm(A) and tet(O) genes; and 2 isolates carrying the erm(A), tet(M), and tet(O) genes. The resistance of all erm(A)-containing isolates was inducible, but the isolates could be divided into two groups on the basis of erythromycin MICs of either >128 or 1 to 4 μg/ml. The remaining 17 isolates included 15 isolates carrying the erm(B) gene and 2 isolates carrying both the erm(B) and the mef(A) genes, with all 17 carrying the tet(M) gene. Of these, 12 carried Tn916-Tn1545-like conjugative transposons. Conjugal transfer experiments demonstrated that the tet(O) gene moved with and without the erm(A) gene and with the mef(A) gene. These studies, together with the results of pulsed-field gel electrophoresis experiments and hybridization assays with DNA probes specific for the tet(O), erm(A), and mef(A) genes, suggested a linkage of tet(O) with either erm(A) or mef(A) in erythromycin- and tetracycline-resistant S. pyogenes isolates. By amplification and sequencing experiments, we detected the tet(O) gene ca. 5.5 kb upstream from the mef(A) gene. This is the first report demonstrating the presence of the tet(O) gene in S. pyogenes and showing that it may be linked with another gene and can be moved by conjugation from one chromosome to another.


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