An lnu(A)-Carrying Multi-Resistance Plasmid Derived from Sequence Type 3 Methicillin-Resistant Staphylococcus
Shih-Cheng Chang1,2, Lee-Chung Lin1, Jang-Jih Lu1,2,3
1Department of Laboratory Medicine, Linkou Chang Gung Memorial Hospitalgrid.413801.f, Taoyuan, Taiwan.
Abstract:
Methicillin-resistant Staphylococcus lugdunensis (MRSL) strains showing resistance to several common antibiotics have been reported recently. Sequence type (ST) 3 MRSL carrying SCCmec types IV, V, or Vt is the major lineage associated with health care-associated infections. We aimed to investigate the distribution and dissemination of antimicrobial resistance determinants in this lineage. Two representative ST3-MRSL strains, CGMH-SL131 (SCCmec V) and CGMH-SL138 (SCCmec IV), were subjected to whole-genome sequencing. Detection of antibiotic resistance genes and screening of susceptibility patterns were performed for 30 ST3-MRSL and 16 ST6-MRSL strains via PCR and standard methods. Except for mecA and blaZ, antimicrobial resistance genes were located within two plasmids: a 28.6 kb lnu(A)-carrying plasmid (pCGMH_SL138) in CGMH-SL138 and a 26 kb plasmid carrying non-lnu(A) resistance genes (pCGMH_SL131) in CGMH-SL131. Both plasmids shared common genetic features with multiple copies of IS257 flanked by genes conferring resistance to aminoglycoside (aacA-aphD and aadD), TET (tetk), and cadmium (cadDX) and tolerance to chlorhexidine (qacA/R); however, only pCGMH_SL138 harbored lnu(A) that conferred resistance to lincomycin and rep13 that encodes a replication initiation protein. Unlike ST6-MRSL, none of the ST3-MRSL isolates contained the ermA gene. Instead, most isolates harbored lnu(A) (20/30, 66.7%), and several other resistance genes found on pCGMH_SL138. These isolates and transformants containing pCGMH_SL138 exhibited susceptibility to ERY and higher MICs for lincomycin and aforementioned antibiotics. A novel lnu(A)-carrying plasmid, pCGMH_SL138, that harbored a multiresistance gene cluster, was identified in ST3-MRSL strains and may contribute to the dissemination of antibiotic resistance in staphylococci.
Insights
Methicillin-resistant Staphylococcus lugdunensis (MRSL) sequence type 3 strains harbor novel plasmids carrying multiple antibiotic resistance genes. These findings highlight a potential mechanism for the spread of antimicrobial resistance in healthcare settings.
Area of Science:
- Microbiology
- Genetics
- Infectious Diseases
Background:
- Methicillin-resistant Staphylococcus lugdunensis (MRSL) is an emerging pathogen associated with healthcare-associated infections.
- Sequence type (ST) 3 MRSL, particularly those carrying SCCmec types IV, V, or Vt, represents a significant lineage driving these infections.
Purpose of the Study:
- To investigate the distribution and dissemination of antimicrobial resistance determinants within the ST3 MRSL lineage.
- To characterize the genetic elements, specifically plasmids, responsible for antibiotic resistance in ST3 MRSL.
Main Methods:
- Whole-genome sequencing of two representative ST3 MRSL strains (CGMH-SL131 and CGMH-SL138).
- Polymerase chain reaction (PCR) and standard microbiological methods to detect antibiotic resistance genes and assess susceptibility patterns in 30 ST3 MRSL and 16 ST6 MRSL strains.
Main Results:
- Two distinct plasmids were identified: pCGMH_SL138 (28.6 kb) carrying lnu(A) and pCGMH_SL131 (26 kb) carrying non-lnu(A) resistance genes.
- Both plasmids contained IS257 elements and genes for aminoglycoside, TET, cadmium resistance, and chlorhexidine tolerance.
- A novel lnu(A)-carrying plasmid, pCGMH_SL138, was identified in 66.7% of ST3 MRSL isolates, conferring resistance to lincomycin and other antibiotics, but not ermA, unlike ST6 MRSL.
Conclusions:
- A novel lnu(A)-carrying plasmid, pCGMH_SL138, harboring a multiresistance gene cluster, was identified in ST3 MRSL strains.
- This plasmid may play a crucial role in the dissemination of antibiotic resistance among staphylococci.
- Understanding these resistance mechanisms is vital for controlling MRSL infections in healthcare environments.
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