Necrotrophism Is a Quorum-Sensing-Regulated Lifestyle in Bacillus thuringiensis

How pathogenic bacteria infect and kill their host is currently widely investigated. In comparison, the fate of pathogens after the death of their host receives less attention. We studied Bacillus thuringiensis (Bt) infection of an insect host, and show that NprR, a quorum sensor, is active after death of the insect and allows Bt to survive in the cadavers as vegetative cells. Transcriptomic analysis revealed that NprR regulates at least 41 genes, including many encoding degradative enzymes or proteins involved in the synthesis of a nonribosomal peptide named kurstakin. These degradative enzymes are essential in vitro to degrade several substrates and are specifically expressed after host death suggesting that Bt has an active necrotrophic lifestyle in the cadaver. We show that kurstakin is essential for Bt survival during necrotrophic development. It is required for swarming mobility and biofilm formation, presumably through a pore forming activity. A nprR deficient mutant does not develop necrotrophically and does not sporulate efficiently in the cadaver. We report that necrotrophism is a highly regulated mechanism essential for the Bt infectious cycle, contributing to spore spreading

The source of hydrogen sulfide in anoxic sediment

Putrefactive hydrogen sulfide production in the upper 4 cm of sediment in two small freshwater and eutrophic Southeast Michigan, U.S.A., lakes ranged from 0.13 to 1.51 with an average of 0.46 mg S l-1 day-1. Sulfate reductive production of hydrogen sulfide at the same sites ranged from 0.7 to 3.2 with an average of 1.54 mg S l-1 day-1. Putrefactive hydrogen sulfide production represented 5.1-53% (average of 18.3-27.6%) of the total hydrogen sulfide produced at the two lakes over an April-October study period. 35S labeled substrates were used to estimate hydrogen sulfide production rates.Proteolytic bacteria averaged 2.2 x 104 cells ml-1 sediment whereas sulfate reducers averaged 4.8 x 102 cells ml-1 sediment. Putrefactive hydrogen sulfide production correlated highly with numbers of proteolytic bacteria (r2 = 0.84) but the correlation between sulfate reduction and sulfate reducing bacteria was low (r2 = 0.13).Interstitial soluble inorganic sulfate, protein and organic carbon were not closely correlated with hydrogen sulfide production rates or bacteria enumeration results. Natural substrate concentrations (Sn) used to estimate hydrogen sulfide production were supported by kinetic bioassay results.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/25926/1/0000489.pd