Use of Fatty Acid Methyl Ester Profiles for Discrimination of Bacillus cereus T-Strain Spores Grown on Different Media

Author:

Ehrhardt Christopher J.12,Chu Vivian12,Brown TeeCie13,Simmons Terrie L.12,Swan Brandon K.4,Bannan Jason5,Robertson James M.2

Affiliation:

1. Federal Bureau of Investigation, Quantico, Virginia 22135

2. Counterterrorism and Forensic Science Research Unit, Federal Bureau of Investigation, Quantico, Virginia 22135

3. Department of Biochemistry and Molecular Biology, Oklahoma State University, Stillwater, Oklahoma 74078

4. Marine Science Program and Department of Earth Science, University of California at Santa Barbara, Santa Barbara, California 93106

5. Chemical and Biological Sciences Unit, FBI Laboratory Division, Quantico, Virginia 22135

Abstract

ABSTRACT The goal of this study was to determine if cellular fatty acid methyl ester (FAME) profiling could be used to distinguish among spore samples from a single species ( Bacillus cereus T strain) that were prepared on 10 different medium formulations. To analyze profile differences and identify FAME biomarkers diagnostic for the chemical constituents in each sporulation medium, a variety of statistical techniques were used, including nonmetric multidimensional scaling (nMDS), analysis of similarities (ANOSIM), and discriminant function analysis (DFA). The results showed that one FAME biomarker, oleic acid (18:1 ω9c), was exclusively associated with spores grown on Columbia agar supplemented with sheep blood and was indicative of blood supplements that were present in the sporulation medium. For spores grown in other formulations, multivariate comparisons across several FAME biomarkers were required to discern profile differences. Clustering patterns in nMDS plots and R values from ANOSIM revealed that dissimilarities among FAME profiles were most pronounced when spores grown with disparate sources of complex additives or protein supplements were compared ( R > 0.8), although other factors also contributed to FAME differences. DFA indicated that differentiation could be maximized with a targeted subset of FAME variables, and the relative contributions of branched FAME biomarkers to group dissimilarities changed when different media were compared. When taken together, these analyses indicate that B. cereus spore samples grown in different media can be resolved with FAME profiling and that this may be a useful technique for providing intelligence about the production methods of Bacillus organisms in a forensic investigation.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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