| Literature DB >> 28316142 |
Wouter Suring1, Karen Meusemann2,3,4, Alexander Blanke5, Janine Mariën1, Tim Schol1, Valeria Agamennone1, Anna Faddeeva-Vakhrusheva1, Matty P Berg1,6, Abraham Brouwer1,7, Nico M van Straalen1, Dick Roelofs1.
Abstract
Beta-lactam biosynthesis was thought to occur only in fungi and bacteria, but we recently reported the presence of isopenicillin N synthase in a soil-dwelling animal, Folsomia candida. However, it has remained unclear whether this gene is part of a larger beta-lactam biosynthesis pathway and how widespread the occurrence of penicillin biosynthesis is among animals. Here, we analysed the distribution of beta-lactam biosynthesis genes throughout the animal kingdom and identified a beta-lactam gene cluster in the genome of F. candida (Collembola), consisting of isopenicillin N synthase (IPNS), δ-(L-α-aminoadipoyl)-L-cysteinyl-D-valine synthetase (ACVS), and two cephamycin C genes (cmcI and cmcJ) on a genomic scaffold of 0.76 Mb. All genes are transcriptionally active and are inducible by stress (heat shock). A beta-lactam compound was detected in vivo using an ELISA beta-lactam assay. The gene cluster also contains an ABC transporter which is coregulated with IPNS and ACVS after heat shock. Furthermore, we show that different combinations of beta-lactam biosynthesis genes are present in over 60% of springtail families, but they are absent from genome- and transcript libraries of other animals including close relatives of springtails (Protura, Diplura and insects). The presence of beta-lactam genes is strongly correlated with an euedaphic (soil-living) lifestyle. Beta-lactam genes IPNS and ACVS each form a phylogenetic clade in between bacteria and fungi, while cmcI and cmcJ genes cluster within bacteria. This suggests a single horizontal gene transfer event most probably from a bacterial host, followed by differential loss in more recently evolving species.Entities:
Keywords: Collembola; antibiotic biosynthesis; gene expression; horizontal gene transfer
Mesh:
Substances:
Year: 2017 PMID: 28316142 DOI: 10.1111/mec.14109
Source DB: PubMed Journal: Mol Ecol ISSN: 0962-1083 Impact factor: 6.185