This also relates to previous observations that bacterial group II introns tend to be located within mobile DNA elements such as plasmids, IS elements, transposons or pathogenicity islands (PAI), which could account for their spread among check details bacteria [44–46]. Based on our results, it is reasonable to suggest that MGEs have played a key role in the transmission of the cereulide gene cluster. In many cases, plasmids encode passenger genes originated via HGT that generally confer adaptive functions to the host cell, the classic example being
antibiotic resistance genes. For instance, the NRPS gene cluster responsible for the production of β-lactam antibiotics (e.g. penicillins and cephalosporins) was proved to be transmitted by HGT from bacteria to bacteria and from bacteria to fungi [47, 48]. This is also the general mode for toxin evolution [49, 50]. In contrast,
as a natural analog, a recent study reported that a vertical transmission (VT) origin rather than a HGT for the vlm gene cluster in Streptomyces spp. Although there is a significant structure Geneticin clinical trial and toxicology similarity between valinomycin and cereulide and an organizational similarity between the vlm gene cluster and the ces gene cluster, they are highly divergent from each other at the DNA level [51]. They may also have quite different evolution history. The conjugative and transfer promoting capacities of the emetic plasmids were also assessed by bi- and tri-parental matings, respectively. None were indicative of self-conjugative or mobilizable activities, at least under the conditions used in the assay (detection limit of 10-7 T/R) (data not shown). Yet, the emetic strains can host the conjugative plasmid pXO16, which could be transferred from its native B. thuringiensis sv. israelensis to the emetic strains and, subsequently from the emetic strains to the original B. thuringiensis sv. israelensis host [52]. An important concern arising from this study is that the cereulide gene cluster may have the potential
to be transmitted by transposition and, therefore, if the emetic strain can randomly encounter the conjugative plasmid pXO16 in nature, transposition ID-8 of the cereulide gene cluster into pXO16 might happen at a low frequency, and as a consequence the resulting emetic pXO16, crossing boundaries within the B. cereus group by conjugation, could pose a serious Selleck Peptide 17 public health issue. Conclusion Emetic B. cereus group isolates display more variations than originally thought. The cereulide biosynthesis gene cluster was present in different hosts (B. cereus sensu stricto and B. weihenstephanensis), which have different chromosomal background and display different genomic locations (plasmids vs. chromosome). The sequences of cereulide genetic determinants are diverse and coevolved with the host.