A mobile genetic element profoundly increases heat resistance of bacterial spores

• Published in: The ISME Journal 2016-11, Vol.10 (11), p.2633-2642
• Main Authors: Berendsen, Erwin M, Boekhorst, Jos, Kuipers, Oscar P, Wells-Bennik, Marjon H J
• Format: Article
• Language: English
• Subjects: 45/43; 45/70; 631/337; Bacillaceae; Bacillus subtilis; Bacillus subtilis - chemistry; Bacillus subtilis - genetics; Bacillus subtilis - metabolism; Bacteria; Bacterial Proteins - genetics; Bacterial Proteins - metabolism; Biomedical and Life Sciences; DNA Transposable Elements; Ecology; Evolutionary Biology; Heat resistance; Hot Temperature; Life Sciences; Microbial Ecology; Microbial Genetics and Genomics; Microbiology; Operon; Original; original-article; Spores, Bacterial - chemistry; Spores, Bacterial - genetics; Spores, Bacterial - metabolism
• ISSN: 1751-7362; 1751-7370
• DOI: 10.1038/ismej.2016.59

Bacterial endospores are among the most resilient forms of life on earth and are intrinsically resistant to extreme environments and antimicrobial treatments. Their resilience is explained by unique cellular structures formed by a complex developmental process often initiated in response to nutrient deprivation. Although the macromolecular structures of spores from different bacterial species are similar, their resistance to environmental insults differs widely. It is not known which of the factors attributed to spore resistance confer very high-level heat resistance. Here, we provide conclusive evidence that in Bacillus subtilis, this is due to the presence of a mobile genetic element (Tn 1546 -like) carrying five predicted operons, one of which contains genes that encode homologs of SpoVAC, SpoVAD and SpoVAEb and four other genes encoding proteins with unknown functions. This operon, named spoVA 2mob , confers high-level heat resistance to spores. Deletion of spoVA 2mob in a B. subtilis strain carrying Tn 1546 renders heat-sensitive spores while transfer of spoVA 2mob into B. subtilis 168 yields highly heat-resistant spores. On the basis of the genetic conservation of different spoVA operons among spore-forming species of Bacillaceae , we propose an evolutionary scenario for the emergence of extremely heat-resistant spores in B. subtilis , B. licheniformis and B. amyloliquefaciens . This discovery opens up avenues for improved detection and control of spore-forming bacteria able to produce highly heat-resistant spores.