Application of Long-Read Whole-Genome Sequencing to Clarify Genotypic-Phenotypic Discrepancies in Methicillin-Resistant <i>Staphylococcus aureus</i>
Abstract
<b>Background/Objectives</b>: The Korean Global Antimicrobial Resistance Surveillance System monitors bloodstream <i>Staphylococcus aureus</i> infections by combining antimicrobial susceptibility testing (AST) with conventional polymerase chain reaction (PCR). Considering the clinical significance of methicillin-resistant <i>S. aureus</i> (MRSA), we performed an in-depth analysis of isolates showing genotypic-phenotypic discrepancies. <b>Methods</b>: Isolates were collected from designated collection centers in the Republic of Korea between 2017 and 2024. The 30 μg cefoxitin disk diffusion method was used to define the phenotypes. PCR targeting <i>mecA</i> and the staphylococcal cassette chromosome <i>mec</i> (SCC<i>mec</i>) was used to identify genotypes through gel electrophoresis. Long-read whole-genome sequencing (WGS) was performed using the Revio system (Pacific Biosciences) for isolates exhibiting discrepancies between phenotypes and genotypes. <b>Results</b>: In total, 5808 isolates were screened, and seven cases of genotypic-phenotypic discrepancies were identified, including one infant and six elderly patients with chromosomal SCC<i>mec</i> type IV. Although WGS confirmed intact PCR primer-binding sites, structural alterations were observed: three isolates had normal-length <i>mecA</i> and <i>mecR1</i>, two had partial deletions in <i>mecA</i>, and two featured either <i>mecA</i> or <i>mecR1</i> split into two proteins. Notably, although the six isolates with intact <i>mecR1</i> genes matched the nucleotide length of SCC<i>mec</i> type IV, their sequences exhibited high homology with SCC<i>mec</i> type II. <b>Conclusions</b>: Despite the presence of <i>mecA</i>, the non-standard configuration of regulatory genes within the SCC<i>mec</i> elements suppressed actual resistance expression. Because conventional PCR focusing on partial gene segments could overlook such phenotypic traits, the meticulous observation and implementation of WGS are crucial for the accurate characterization of genotypic-phenotypic discrepancies.