Cytotoxicity and apoptosis induction of Bacillus vallismortis BIT-33 metabolites on colon cancer carcinoma cells

J Appl Microbiol. 2008 Mar;104(3):796-807. doi: 10.1111/j.1365-2672.2007.03615.x. Epub 2007 Nov 15.

Abstract

Aims: The objective of this research was to isolate and identify a cytotoxic marine bacterium, BIT-33, and to investigate the apoptosis effects of its metabolite on colon cancer cells.

Method and results: We isolated 93 marine bacteria from seawater samples. Of these, strain BIT-33 exhibited the strongest cytotoxic activity on three colon cancer cells (HT-29, SW480 and HCT116). Biochemical tests and 16S rDNA sequencing of this strain allowed us to identify BIT-33 as a strain of Bacillus vallismortis. The cytotoxic compound from B. vallismortis BIT-33 was purified by reverse-phase high-performance liquid chromatography. Direct cytotoxic effect of the compound was measured by 3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazoliumbromide assay. The compound induced apoptosis of colon cancer cells, as indicated by DNA fragmentation of agarose gel electrophoresis, flow cytometric analysis (sub-G(1) method) and annexin V staining.

Conclusion: The cytotoxic compound from B. vallismortis BIT-33 was purified, and the compound showed direct cytotoxic and apoptotic effects on colon cancer cells in a dose- and time-dependent manner.

Significance and impact of the study: Taken together, our results suggest that the compound from B. vallismortis BIT-33 could be a candidate for the development of apoptosis-specific anti-tumour agents. This study indicated that marine bacteria could be an important source of cytotoxic metabolites.

MeSH terms

  • Apoptosis / drug effects
  • Bacillus / chemistry*
  • Cell Line, Tumor
  • Cell Survival
  • Colonic Neoplasms / drug therapy*
  • Colonic Neoplasms / pathology
  • Cytotoxins / isolation & purification*
  • Cytotoxins / therapeutic use
  • DNA Fragmentation
  • Dose-Response Relationship, Drug
  • Electrophoresis, Agar Gel
  • Flow Cytometry
  • Humans
  • Seawater
  • Staining and Labeling
  • Time Factors

Substances

  • Cytotoxins