Raman spectra identify vancomycin-resistant phenotypes and their transcriptomic features in Staphylococcus aureus
This article has been Reviewed by the following groups
Listed in
- Evaluated articles (Arcadia Science)
Abstract
Staphylococcus aureus is a pathogenic bacterium that has caused multiple epidemics linked with the emergence of new antibiotic resistance. Vancomycin is the first-line antibiotic to treat methicillin-resistant S. aureus (MRSA) infections. However, several types of vancomycin-non-susceptible MRSA strains have been isolated from patients to date. Rapid assessment of their resistance levels and underlying molecular profiles is crucial for preventing their spread and counteracting resistance; however, the broad resistance spectrum and the diversity of genetic changes have impeded this practice. Here, we demonstrate that the vancomycin resistance levels of various MRSA strains can be determined using dimension-reduced Raman spectra obtained from single cells. The transcriptome profiles of the different strains can also be predicted from their dimensionally reduced Raman spectra by simple linear regression. This Raman-transcriptome correspondence allows us to map the transcriptome components onto dimension-reduced Raman space and characterize groups of genes associated with different phenotypes. Furthermore, single-cell Raman spectra predicted a cell strain with greater phenotypic heterogeneity, which was confirmed by single-cell growth analysis. Overall, our results demonstrate the efficacy of Raman spectroscopy in identifying resistant phenotypes, their associated gene expression features, and intrapopulation phenotypic heterogeneity.
Article activity feed
-
n this study, we introduced a method for representing transcriptome components usinglow-dimensional Raman LDA axes based on Raman-transcriptome linear correspondence (Fig.4).
it would also be valuable to see which Raman wavenumbers drive the LDA axes to see if they make conceptual sense and are not just noisy artifacts. by eye, the representative spectra in fig 1c are very similar, so it would be good to see that the differences between the strains are driven by real differences in peaks
-
The transcriptomes of the nine S. aureus strains were ob-tained from the public database
were the transcriptomes (or at least a subset) validated in-house? some more details about how the transcriptome data was used would be very beneficial to the reader.
-