Infrared microspectroscopy allows for detailed characterization of functional groups at subcellular levels in plants. In this study, barley leaves were inoculated with Blumeria graminis f. sp. hordei (Bgh, adapted) and B. graminis f. sp. tritici (Bgt, nonadapted). Globar-based transmission Fourier transform infrared (gFTIR) microspectroscopy equipped with an upgraded high-resolution focal plane array (FPA) detector which enabled the rapid acquisition of high magnification imaging with a 3.3-μm × 3.3-μm capacity, was employed to quantitatively analyse the cell wall (CW) modification over individual leaf cells in response to attempted penetration at 24 hours post-inoculation. Univariate and multivariate analyses of gFTIR spectra revealed distinct changes in several CW functional groups upon attempted penetration by Bgt, with significant increases in the integrated areas of cellulose, hemicellulose, methyl-esterified pectins and lipid regions compared to cells without penetration. Notably, neither guaiacyl (G) nor syringyl (S) lignin increased significantly in CWs near Bgt penetration sites relative to nonpenetrating controls, though the G/S ratio was higher than in Bgh-penetrated sites. These findings suggest early and rapid CW modifications occur during the nonhost resistance to Bgt. This study also confirms previous results obtained using synchrotron-based FTIR (sFTIR), demonstrating that both gFTIR and sFTIR are valuable for studying plant CW apposition, with gFTIR being more accessible and rapid for imaging over large areas with compatible quality and resolution to sFTIR.
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