Unearthing new ccr genes and SCC elements in staphylococci through genome mining.
Jianguo HuangJinhe XiaoXiaokun WangXuemei XueYadong MaZiqian ZhangLiangjun ZhengMuhammad ZafirPilong LiuXin ZhaoAnders Rhod LarsenHuping XuePublished in: The Journal of infectious diseases (2024)
The SCCmec typing is crucial for investigating methicillin-resistant S. aureus, relying primarily on the combination of ccr and mec gene complexes. To date, 19 ccr genes and 10 ccr gene complexes have been identified, forming 15 SCCmec types. With the vast release of bacterial genome sequences, mining the database for novel ccr gene complexes and SCC/SCCmec elements could enhance MRSA epidemiological studies. In this study, we identified 12 novel ccr genes (6 ccrA, 3 ccrB and 3 ccrC) through mining of the NCBI database, which forming 12 novel ccr gene complexes and 10 novel SCC elements. Overexpression of five groups of novel Ccr recombinases (CcrA9B3, CcrA10B1, CcrC3, CcrC4, and CcrC5) in a mutant MRSA strain lacking the ccr gene and extrachromosomal circular intermediate (ciSCC) production significantly promoted ciSCC production, demonstrating their biological activity. This discovery provides an opportunity to advance MRSA epidemiological research and develop database-based bacterial typing methods.
Keyphrases
- genome wide
- dendritic cells
- genome wide identification
- regulatory t cells
- staphylococcus aureus
- copy number
- methicillin resistant staphylococcus aureus
- dna methylation
- genome wide analysis
- transcription factor
- small molecule
- emergency department
- immune response
- antimicrobial resistance
- adverse drug
- single cell
- drug induced