Tobacco, Microbes, and Carcinogens: Correlation Between Tobacco Cure Conditions, Tobacco-Specific Nitrosamine Content, and Cured Leaf Microbial Community

• Published in: Microbial ecology 2016-07, Vol.72 (1), p.120-129
• Main Authors: Law, Audrey D., Fisher, Colin, Jack, Anne, Moe, Luke A.
• Format: Article
• Language: English
• Subjects: Actinobacteria; Bacteria - classification; Bacteria - enzymology; Bacteria - isolation & purification; Biomedical and Life Sciences; Carcinogens - analysis; DNA, Bacterial - genetics; Ecology; ENVIRONMENTAL MICROBIOLOGY; Firmicutes; Geoecology/Natural Processes; Life Sciences; Microbial activity; Microbial Ecology; Microbiology; Nature Conservation; Nicotiana - chemistry; Nicotiana - microbiology; Nitrate Reductase - genetics; Nitrate reduction; Nitrates - analysis; Nitrites - analysis; Nitrosamines; Nitrosamines - analysis; Plant Leaves - chemistry; Plant Leaves - microbiology; Proteobacteria; Relative humidity; RNA, Ribosomal, 16S - genetics; Temperature; Tobacco; Water Quality/Water Pollution
• ISSN: 0095-3628; 1432-184X
• DOI: 10.1007/s00248-016-0754-4

Tobacco-specific nitrosamines are carcinogenic N-nitrosamine compounds present at very low levels in freshly harvested tobacco leaves that accumulate during leaf curing. Formation of N-nitrosamine compounds is associated with high nitrate levels in the leaf at harvest, and nitrate is presumed to be the source from which the N-nitrosation species originates. More specifically, nitrite is considered to be a direct precursor, and nitrite is linked with N-nitrosation in many environmental matrices where it occurs via microbial nitrate reduction. Here, we initiate work exploring the role of leaf microbial communities in formation of tobacco-specific nitrosamines. Leaves from burley tobacco line TN90H were air cured under various temperature and relative humidity levels, and 22 cured tobacco samples were analyzed for their microbial communities and leaf chemistry. Analysis of nitrate, nitrite, and total tobacco-specific nitrosamine levels revealed a strong positive correlation between the three variables, as well as a strong positive correlation with increasing relative humidity during cure conditions. 16S rRNA gene amplicon sequencing was used to assess microbial communities in each of the samples. In most samples, Proteobacteria predominated at the phylum level, accounting for >90 % of the OTUs. However, a distinct shift was noted among members of the high tobacco-specific nitrosamine group, with increases in Firmicutes and Actinobacteria. Several OTUs were identified that correlate strongly (positive and negative) with tobacco-specific nitrosamine content. Copy number of bacterial nitrate reductase genes, obtained using quantitative PCR, did not correlate strongly with tobacco-specific nitrosamine content. Incomplete denitrification is potentially implicated in tobacco-specific nitrosamine levels.