scholarly journals Association of a Penicillin Resistance Gene with a Tetracycline Resistance Plasmid (PTP-2) in Staphylococcus aureus

1976 ◽  
Vol 9 (4) ◽  
pp. 706-712 ◽  
Author(s):  
M. Kono ◽  
M. Sasatsu
2008 ◽  
Vol 53 (2) ◽  
pp. 776-778 ◽  
Author(s):  
Kristina Kadlec ◽  
Stefan Schwarz

ABSTRACT A novel trimethoprim resistance gene, designated dfrK, was detected in close proximity to the tetracycline resistance gene tet(L) on the ca. 40-kb plasmid pKKS2187 in a porcine methicillin (meticillin)-resistant Staphylococcus aureus isolate of sequence type 398. The dfrK gene encodes a 163-amino-acid dihydrofolate reductase that differs from all so-far-known dihydrofolate reductases.


2000 ◽  
Vol 182 (12) ◽  
pp. 3345-3352 ◽  
Author(s):  
Alice E. Simpson ◽  
Ronald A. Skurray ◽  
Neville Firth

ABSTRACT Transcription of the tetA(K) tetracycline resistance determinant encoded by an IS257-flanked cointegrated copy of a pT181-like plasmid, located within the chromosomal mecregion of a methicillin-resistant Staphylococcus aureusisolate, has been investigated. The results demonstrated that transcription of tetA(K) in this strain is directed by both an IS257-derived hybrid promoter, which is stronger than the native tetA(K) promoter in the autonomous form of pT181, and a complete outwardly directed promoter identified within one end of IS257. Despite lower gene dosage, the chromosomal configuration was shown to afford a higher level of resistance than that mediated by pT181 in an autonomous multicopy state. Furthermore, competition studies revealed that a strain carrying the chromosomaltetA(K) determinant exhibited a higher level of fitness in the presence of tetracycline but not in its absence. This finding suggests that tetracycline has been a selective factor in the emergence of strains carrying a cointegrated pT181-like plasmid in their chromosomes. The results highlight the potential of IS257to influence the expression of neighboring genes, a property likely to enhance its capacity to mediate advantageous genetic rearrangements.


2009 ◽  
Vol 54 (2) ◽  
pp. 915-918 ◽  
Author(s):  
Kristina Kadlec ◽  
Stefan Schwarz

ABSTRACT A novel plasmid-borne resistance gene cluster comprising the genes erm(T) for macrolide-lincosamide-streptogramin B resistance, dfrK for trimethoprim resistance, and tet(L) for tetracycline resistance was identified in a porcine methicillin-resistant Staphylococcus aureus sequence type 398 (ST398) strain. This erm(T)-dfrK-tet(L) region was flanked by copies of the novel IS element ISSau10. The erm(T) region resembled that of Streptococcus pyogenes plasmid pRW35. The erm(T) gene of pKKS25 was expressed constitutively due to a 57-bp deletion in the erm(T) translational attenuator.


2010 ◽  
Vol 55 (1) ◽  
pp. 373-375 ◽  
Author(s):  
Andrea T. Feßler ◽  
Kristina Kadlec ◽  
Stefan Schwarz

ABSTRACTA novel apramycin resistance gene,apmA, was detected on the ca.-40-kb resistance plasmid pAFS11 from bovine methicillin-resistantStaphylococcus aureus(MRSA) of sequence type 398 (ST398). TheapmAgene coded for a protein of 274 amino acids that was related only distantly to acetyltransferases involved in chloramphenicol or streptogramin A resistance. NsiI deletion ofapmAresulted in a 16- to 32-fold decrease in the apramycin MICs. AnapmA-specific PCR identified this gene in one additional bovine and four porcine MRSA ST398 isolates.


2016 ◽  
Vol 60 (7) ◽  
pp. 4401-4403 ◽  
Author(s):  
Jesper Larsen ◽  
Julie Clasen ◽  
Julie E. Hansen ◽  
Wilhelm Paulander ◽  
Andreas Petersen ◽  
...  

ABSTRACTThe tetracycline resistance genetet(K) was shown to be integrated within the predominant staphylococcal cassette chromosomemec(SCCmec) element of Danish livestock-associated methicillin-resistantStaphylococcus aureusCC398 (LA-MRSA CC398). These LA-MRSA CC398 isolates already possessedtet(M), but the acquisition oftet(K) significantly improved their fitness at sublethal concentrations of tetracycline. Becausetet(K) is genetically linked to SCCmec, the use of tetracycline in food animals may have contributed to the successful spread of LA-MRSA CC398.


Sign in / Sign up

Export Citation Format

Share Document