Evolutionary ecology of beta‐lactam gene clusters in animals
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 wid...
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Veröffentlicht in: | Molecular ecology 2017-06, Vol.26 (12), p.3217-3229 |
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creator | Suring, Wouter Meusemann, Karen Blanke, Alexander Mariën, Janine Schol, Tim Agamennone, Valeria Faddeeva‐Vakhrusheva, Anna Berg, Matty P. Brouwer, Abraham Straalen, Nico M. Roelofs, Dick |
description | 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. |
doi_str_mv | 10.1111/mec.14109 |
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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.</description><identifier>ISSN: 0962-1083</identifier><identifier>EISSN: 1365-294X</identifier><identifier>DOI: 10.1111/mec.14109</identifier><identifier>PMID: 28316142</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>ABC transporter ; Amides ; Animals ; antibiotic biosynthesis ; Aquatic insects ; Arthropod Proteins - genetics ; Arthropods - enzymology ; Arthropods - genetics ; Assaying ; Bacteria ; beta-Lactams ; Biological evolution ; Biosynthesis ; Cephamycins ; Collembola ; Correlation ; Ecology ; Enzyme-linked immunosorbent assay ; Evolution ; Folsomia candida ; Fungi ; Gene clusters ; gene expression ; Gene transfer ; Genes ; Genomes ; Heat shock ; horizontal gene transfer ; Isopenicillin N synthase ; Multigene Family ; Oxidoreductases - genetics ; Penicillin ; Peptide Synthases - genetics ; Phylogeny ; Soils ; Valine ; β-Lactam antibiotics</subject><ispartof>Molecular ecology, 2017-06, Vol.26 (12), p.3217-3229</ispartof><rights>2017 John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3889-cef37aa140d8abf59a1abf48c8d53ebb7d638b931ace0da514211198a96ffea53</citedby><cites>FETCH-LOGICAL-c3889-cef37aa140d8abf59a1abf48c8d53ebb7d638b931ace0da514211198a96ffea53</cites><orcidid>0000-0003-3954-3590</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fmec.14109$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fmec.14109$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28316142$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suring, Wouter</creatorcontrib><creatorcontrib>Meusemann, Karen</creatorcontrib><creatorcontrib>Blanke, Alexander</creatorcontrib><creatorcontrib>Mariën, Janine</creatorcontrib><creatorcontrib>Schol, Tim</creatorcontrib><creatorcontrib>Agamennone, Valeria</creatorcontrib><creatorcontrib>Faddeeva‐Vakhrusheva, Anna</creatorcontrib><creatorcontrib>Berg, Matty P.</creatorcontrib><creatorcontrib>Brouwer, Abraham</creatorcontrib><creatorcontrib>Straalen, Nico M.</creatorcontrib><creatorcontrib>Roelofs, Dick</creatorcontrib><creatorcontrib>1KITE Basal Hexapod consortium</creatorcontrib><creatorcontrib>the 1KITE Basal Hexapod consortium</creatorcontrib><title>Evolutionary ecology of beta‐lactam gene clusters in animals</title><title>Molecular ecology</title><addtitle>Mol Ecol</addtitle><description>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.</description><subject>ABC transporter</subject><subject>Amides</subject><subject>Animals</subject><subject>antibiotic biosynthesis</subject><subject>Aquatic insects</subject><subject>Arthropod Proteins - genetics</subject><subject>Arthropods - enzymology</subject><subject>Arthropods - genetics</subject><subject>Assaying</subject><subject>Bacteria</subject><subject>beta-Lactams</subject><subject>Biological evolution</subject><subject>Biosynthesis</subject><subject>Cephamycins</subject><subject>Collembola</subject><subject>Correlation</subject><subject>Ecology</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Evolution</subject><subject>Folsomia candida</subject><subject>Fungi</subject><subject>Gene clusters</subject><subject>gene expression</subject><subject>Gene transfer</subject><subject>Genes</subject><subject>Genomes</subject><subject>Heat shock</subject><subject>horizontal gene transfer</subject><subject>Isopenicillin N synthase</subject><subject>Multigene Family</subject><subject>Oxidoreductases - genetics</subject><subject>Penicillin</subject><subject>Peptide Synthases - genetics</subject><subject>Phylogeny</subject><subject>Soils</subject><subject>Valine</subject><subject>β-Lactam antibiotics</subject><issn>0962-1083</issn><issn>1365-294X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kM1Kw0AUhQdRbK0ufAEJuNFF2rmZ_MxsBCn1BypuFNwNk8lNSUkyNZMo2fkIPqNP4miqC8F7F2fzcTjnEHIMdAruZhXqKYRAxQ4ZA4sjPxDh0y4ZUxEHPlDORuTA2jWlwIIo2iejgDOIIQzG5GLxYsquLUytmt5DbUqz6j2Teym26uPtvVS6VZW3who9XXa2xcZ6Re2puqhUaQ_JXu4Ej7Y6IY9Xi4f5jb-8v76dXy59zTgXvsacJUpBSDOu0jwSCpyEXPMsYpimSRYzngoGSiPNVOSiuV6CKxHnOaqITcjZ4LtpzHOHtpVVYTWWparRdFYCTwS4TxKHnv5B16ZrapdOgqBxACLgwlHnA6UbY22Dudw0rlHTS6Dya1TpRpXfozr2ZOvYpRVmv-TPig6YDcBrUWL_v5O8W8wHy09nEIEc</recordid><startdate>201706</startdate><enddate>201706</enddate><creator>Suring, Wouter</creator><creator>Meusemann, Karen</creator><creator>Blanke, Alexander</creator><creator>Mariën, Janine</creator><creator>Schol, Tim</creator><creator>Agamennone, Valeria</creator><creator>Faddeeva‐Vakhrusheva, Anna</creator><creator>Berg, Matty P.</creator><creator>Brouwer, Abraham</creator><creator>Straalen, Nico M.</creator><creator>Roelofs, Dick</creator><general>Blackwell Publishing Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>7SS</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3954-3590</orcidid></search><sort><creationdate>201706</creationdate><title>Evolutionary ecology of beta‐lactam gene clusters in animals</title><author>Suring, Wouter ; 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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.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>28316142</pmid><doi>10.1111/mec.14109</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-3954-3590</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | ABC transporter Amides Animals antibiotic biosynthesis Aquatic insects Arthropod Proteins - genetics Arthropods - enzymology Arthropods - genetics Assaying Bacteria beta-Lactams Biological evolution Biosynthesis Cephamycins Collembola Correlation Ecology Enzyme-linked immunosorbent assay Evolution Folsomia candida Fungi Gene clusters gene expression Gene transfer Genes Genomes Heat shock horizontal gene transfer Isopenicillin N synthase Multigene Family Oxidoreductases - genetics Penicillin Peptide Synthases - genetics Phylogeny Soils Valine β-Lactam antibiotics |
title | Evolutionary ecology of beta‐lactam gene clusters in animals |
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