MALDI-TOF Mass Spectrometry Analysis and Human Post-Mortem Microbial Community: A Pilot Study.
Carlo Pietro Campobasso1, Gennaro Mastroianni1, Alessandro Feola1
1Department of Experimental Medicine, Legal Medicine Section, University of Study of Campania "Luigi Vanvitelli", 80138 Naples, Italy.
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) is a fast and affordable method for identifying microbes and analyzing the human post-mortem microbiome (HPM). This technique shows promise for estimating the post-mortem interval (PMI) by tracking microbial changes during decomposition.
Area of Science:
- Forensic microbiology
- Microbial ecology
- Biotechnology
Background:
- The human post-mortem microbiome (HPM) significantly influences decomposition.
- High-throughput sequencing has shown HPM bacterial communities can predict post-mortem interval (PMI).
- Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) offers a rapid and cost-effective method for microbial identification.
Purpose of the Study:
- To evaluate MALDI-TOF MS as a tool for identifying microbes in the HPM.
- To assess the utility of MALDI-TOF MS for studying HPM changes over time.
- To determine if MALDI-TOF MS can aid in PMI estimation.
Main Methods:
- 18 human bodies with post-mortem intervals (PMI) ranging from 24 hours to 15 days were studied.
- Microbiological swabs were collected from five external sites and four internal organs.
- MALDI-TOF MS was used for microbial taxonomic identification.
Main Results:
- The HPM composition shifted significantly over time in both internal organs and skin sites.
- Firmicutes and Proteobacteria were the dominant phyla in the HPM.
- A distinct microbial turnover was observed during decomposition, correlating with PMI.
Conclusions:
- MALDI-TOF MS is a viable, high-throughput method for HPM analysis and PMI estimation due to its speed and reproducibility.
- The technique can detect overall microbial community shifts in prevalent phyla during decomposition.
- Limitations include sensitivity issues inherent to culture-dependent methods and potential bias in identifying novel microbial isolates.
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