TY - JOUR
T1 - Characterization of bacillus subtilis colony biofilms via mass spectrometry and fluorescence imaging
AU - Si, Tong
AU - Li, Bin
AU - Zhang, Ke
AU - Xu, Yiran
AU - Zhao, Huimin
AU - Sweedler, Jonathan V.
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/6/3
Y1 - 2016/6/3
N2 - Colony biofilms of Bacillus subtilis are a widely used model for studying cellular differentiation. Here, we applied matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) to examine cellular and molecular heterogeneity in B. subtilis colony biofilms. From B. subtilis cells cultivated on a biofilm-promoting medium, we detected two cannibalistic factors not found in previous MALDI MSI studies of the same strain under different culturing conditions. Given the importance of cannibalism in matrix formation of B. subtilis biofilms, we employed a transcriptional reporter to monitor matrix-producing cell subpopulations using fluorescence imaging. These two complementary imaging approaches were used to characterize three B. subtilis strains, the wild type isolate NCIB3610, and two mutants, Δspo0A and ΔabrB, with defective and enhanced biofilm phenotypes, respectively. Upon deletion of key transcriptional factors, correlated changes were observed in biofilm morphology, signaling, cannibalistic factor distribution, and matrix-related gene expression, providing new insights on cannibalism in biofilm development. This work underscores the advantages of using multimodal imaging to compare spatial patterns of selected molecules with the associated protein expression patterns, obtaining information on cellular heterogeneity and function not obtainable when using a single method to characterize biofilm formation.
AB - Colony biofilms of Bacillus subtilis are a widely used model for studying cellular differentiation. Here, we applied matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) to examine cellular and molecular heterogeneity in B. subtilis colony biofilms. From B. subtilis cells cultivated on a biofilm-promoting medium, we detected two cannibalistic factors not found in previous MALDI MSI studies of the same strain under different culturing conditions. Given the importance of cannibalism in matrix formation of B. subtilis biofilms, we employed a transcriptional reporter to monitor matrix-producing cell subpopulations using fluorescence imaging. These two complementary imaging approaches were used to characterize three B. subtilis strains, the wild type isolate NCIB3610, and two mutants, Δspo0A and ΔabrB, with defective and enhanced biofilm phenotypes, respectively. Upon deletion of key transcriptional factors, correlated changes were observed in biofilm morphology, signaling, cannibalistic factor distribution, and matrix-related gene expression, providing new insights on cannibalism in biofilm development. This work underscores the advantages of using multimodal imaging to compare spatial patterns of selected molecules with the associated protein expression patterns, obtaining information on cellular heterogeneity and function not obtainable when using a single method to characterize biofilm formation.
KW - biofilm
KW - cell differentiation
KW - fluorescence imaging
KW - mass spectrometry imaging
KW - transcriptional reporter
UR - http://www.scopus.com/inward/record.url?scp=84973545745&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84973545745&partnerID=8YFLogxK
U2 - 10.1021/acs.jproteome.6b00127
DO - 10.1021/acs.jproteome.6b00127
M3 - Article
C2 - 27136705
AN - SCOPUS:84973545745
SN - 1535-3893
VL - 15
SP - 1955
EP - 1962
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 6
ER -