Culturable bacterial microbiota of Plagiodera versicolora (L.) (Coleoptera: Chrysomelidae) and virulence of the isolated strains.
Identifieur interne : 002745 ( Main/Exploration ); précédent : 002744; suivant : 002746Culturable bacterial microbiota of Plagiodera versicolora (L.) (Coleoptera: Chrysomelidae) and virulence of the isolated strains.
Auteurs : Meryem Demirci [Turquie] ; Elif Sevim ; Smail Demir ; Ali SevimSource :
- Folia microbiologica [ 1874-9356 ] ; 2013.
Descripteurs français
- KwdFr :
- ARN ribosomique 16S (génétique), Agents de lutte biologique (MeSH), Amylases (métabolisme), Analyse de séquence d'ADN (MeSH), Animaux (MeSH), Cellulose (métabolisme), Chitinase (métabolisme), Coléoptères (microbiologie), Larve (microbiologie), Microbiote (MeSH), Micrococcus luteus (enzymologie), Micrococcus luteus (isolement et purification), Micrococcus luteus (pathogénicité), Pantoea (enzymologie), Pantoea (isolement et purification), Pantoea (pathogénicité), Peptide hydrolases (métabolisme), Phénotype (MeSH), Rahnella (enzymologie), Rahnella (isolement et purification), Rahnella (pathogénicité), Staphylococcus (enzymologie), Staphylococcus (isolement et purification), Staphylococcus (pathogénicité), Tests de sensibilité microbienne (MeSH), Triacylglycerol lipase (métabolisme), Virulence (MeSH).
- MESH :
- enzymologie : Micrococcus luteus, Pantoea, Rahnella, Staphylococcus.
- génétique : ARN ribosomique 16S.
- isolement et purification : Micrococcus luteus, Pantoea, Rahnella, Staphylococcus.
- microbiologie : Coléoptères, Larve.
- métabolisme : Amylases, Cellulose, Chitinase, Peptide hydrolases, Triacylglycerol lipase.
- pathogénicité : Micrococcus luteus, Pantoea, Rahnella, Staphylococcus.
- Agents de lutte biologique, Analyse de séquence d'ADN, Animaux, Microbiote, Phénotype, Tests de sensibilité microbienne, Virulence.
English descriptors
- KwdEn :
- Amylases (metabolism), Animals (MeSH), Biological Control Agents (MeSH), Cellulose (metabolism), Chitinases (metabolism), Coleoptera (microbiology), Larva (microbiology), Lipase (metabolism), Microbial Sensitivity Tests (MeSH), Microbiota (MeSH), Micrococcus luteus (enzymology), Micrococcus luteus (isolation & purification), Micrococcus luteus (pathogenicity), Pantoea (enzymology), Pantoea (isolation & purification), Pantoea (pathogenicity), Peptide Hydrolases (metabolism), Phenotype (MeSH), RNA, Ribosomal, 16S (genetics), Rahnella (enzymology), Rahnella (isolation & purification), Rahnella (pathogenicity), Sequence Analysis, DNA (MeSH), Staphylococcus (enzymology), Staphylococcus (isolation & purification), Staphylococcus (pathogenicity), Virulence (MeSH).
- MESH :
- chemical , genetics : RNA, Ribosomal, 16S.
- chemical , metabolism : Amylases, Cellulose, Chitinases, Lipase, Peptide Hydrolases.
- enzymology : Micrococcus luteus, Pantoea, Rahnella, Staphylococcus.
- isolation & purification : Micrococcus luteus, Pantoea, Rahnella, Staphylococcus.
- microbiology : Coleoptera, Larva.
- pathogenicity : Micrococcus luteus, Pantoea, Rahnella, Staphylococcus.
- Animals, Biological Control Agents, Microbial Sensitivity Tests, Microbiota, Phenotype, Sequence Analysis, DNA, Virulence.
Abstract
Plagiodera versicolora (Laicharting, 1781) (Coleoptera: Chrysomelidae) is an important forest pest which damages many trees such as willow, poplar, and hazelnut. In order to find new microbes that can be utilized as a possible microbial control agent against this pest, we investigated the culturable bacterial flora of it and tested the isolated bacteria against P. versicolora larvae and adults. We were able to isolate nine bacteria from larvae and adults. The isolates were characterized using a combination of morphological, biochemical, and physiological methods. Additionally, we sequenced the partial sequence of the 16S rRNA gene to verify conventional identification results. Based on characterization studies, the isolates were identified as Staphylococcus sp. Pv1, Rahnella sp. Pv2, Rahnella sp. Pv3, Rahnella sp. Pv4, Rahnella sp. Pv5, Pantoea agglomerans Pv6, Staphylococcus sp. Pv7, Micrococcus luteus Pv8, and Rahnella sp. Pv9. The highest insecticidal activity against larvae and adults was obtained from M. luteus Pv8 with 50 and 40 % mortalities within 10 days after treatment, respectively. Extracellular enzyme activity of the bacterial isolates such as amylase, proteinase, lipase, cellulose, and chitinase was also determined. Consequently, our results show that M. luteus Pv8 might be a good candidate as a possible microbial control agent against P. versicolora and were discussed with respect to biocontrol potential of the bacterial isolates.
DOI: 10.1007/s12223-012-0199-1
PubMed: 23054688
Affiliations:
Links toward previous steps (curation, corpus...)
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microbienne</term><term>Virulence</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Plagiodera versicolora (Laicharting, 1781) (Coleoptera: Chrysomelidae) is an important forest pest which damages many trees such as willow, poplar, and hazelnut. In order to find new microbes that can be utilized as a possible microbial control agent against this pest, we investigated the culturable bacterial flora of it and tested the isolated bacteria against P. versicolora larvae and adults. We were able to isolate nine bacteria from larvae and adults. The isolates were characterized using a combination of morphological, biochemical, and physiological methods. Additionally, we sequenced the partial sequence of the 16S rRNA gene to verify conventional identification results. Based on characterization studies, the isolates were identified as Staphylococcus sp. Pv1, Rahnella sp. Pv2, Rahnella sp. Pv3, Rahnella sp. Pv4, Rahnella sp. Pv5, Pantoea agglomerans Pv6, Staphylococcus sp. Pv7, Micrococcus luteus Pv8, and Rahnella sp. Pv9. The highest insecticidal activity against larvae and adults was obtained from M. luteus Pv8 with 50 and 40 % mortalities within 10 days after treatment, respectively. Extracellular enzyme activity of the bacterial isolates such as amylase, proteinase, lipase, cellulose, and chitinase was also determined. Consequently, our results show that M. luteus Pv8 might be a good candidate as a possible microbial control agent against P. versicolora and were discussed with respect to biocontrol potential of the bacterial isolates.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23054688</PMID><DateCompleted><Year>2013</Year><Month>12</Month><Day>02</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1874-9356</ISSN><JournalIssue CitedMedium="Internet"><Volume>58</Volume><Issue>3</Issue><PubDate><Year>2013</Year><Month>May</Month></PubDate></JournalIssue><Title>Folia microbiologica</Title><ISOAbbreviation>Folia Microbiol (Praha)</ISOAbbreviation></Journal><ArticleTitle>Culturable bacterial microbiota of Plagiodera versicolora (L.) (Coleoptera: Chrysomelidae) and virulence of the isolated strains.</ArticleTitle><Pagination><MedlinePgn>201-10</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1007/s12223-012-0199-1</ELocationID><Abstract><AbstractText>Plagiodera versicolora (Laicharting, 1781) (Coleoptera: Chrysomelidae) is an important forest pest which damages many trees such as willow, poplar, and hazelnut. In order to find new microbes that can be utilized as a possible microbial control agent against this pest, we investigated the culturable bacterial flora of it and tested the isolated bacteria against P. versicolora larvae and adults. We were able to isolate nine bacteria from larvae and adults. The isolates were characterized using a combination of morphological, biochemical, and physiological methods. Additionally, we sequenced the partial sequence of the 16S rRNA gene to verify conventional identification results. Based on characterization studies, the isolates were identified as Staphylococcus sp. Pv1, Rahnella sp. Pv2, Rahnella sp. Pv3, Rahnella sp. Pv4, Rahnella sp. Pv5, Pantoea agglomerans Pv6, Staphylococcus sp. Pv7, Micrococcus luteus Pv8, and Rahnella sp. Pv9. The highest insecticidal activity against larvae and adults was obtained from M. luteus Pv8 with 50 and 40 % mortalities within 10 days after treatment, respectively. Extracellular enzyme activity of the bacterial isolates such as amylase, proteinase, lipase, cellulose, and chitinase was also determined. Consequently, our results show that M. luteus Pv8 might be a good candidate as a possible microbial control agent against P. versicolora and were discussed with respect to biocontrol potential of the bacterial isolates.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Demirci</LastName><ForeName>Meryem</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Biology, Faculty of Arts and Sciences, Recep Tayyip Erdoğan University, Rize-53100, Turkey.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sevim</LastName><ForeName>Elif</ForeName><Initials>E</Initials></Author><Author ValidYN="Y"><LastName>Demir</LastName><ForeName>İsmail</ForeName><Initials>İ</Initials></Author><Author ValidYN="Y"><LastName>Sevim</LastName><ForeName>Ali</ForeName><Initials>A</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2012</Year><Month>10</Month><Day>04</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Folia Microbiol (Praha)</MedlineTA><NlmUniqueID>0376757</NlmUniqueID><ISSNLinking>0015-5632</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D061046">Biological Control Agents</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D012336">RNA, Ribosomal, 16S</NameOfSubstance></Chemical><Chemical><RegistryNumber>9004-34-6</RegistryNumber><NameOfSubstance UI="D002482">Cellulose</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 3.1.1.3</RegistryNumber><NameOfSubstance UI="D008049">Lipase</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 3.2.1.-</RegistryNumber><NameOfSubstance UI="D000681">Amylases</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 3.2.1.14</RegistryNumber><NameOfSubstance UI="D002688">Chitinases</NameOfSubstance></Chemical><Chemical><RegistryNumber>EC 3.4.-</RegistryNumber><NameOfSubstance UI="D010447">Peptide Hydrolases</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D000681" MajorTopicYN="N">Amylases</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D061046" MajorTopicYN="N">Biological Control Agents</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D002482" MajorTopicYN="N">Cellulose</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002688" MajorTopicYN="N">Chitinases</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D001517" MajorTopicYN="N">Coleoptera</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="Y">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D007814" MajorTopicYN="N">Larva</DescriptorName><QualifierName UI="Q000382" MajorTopicYN="N">microbiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008049" MajorTopicYN="N">Lipase</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D008826" MajorTopicYN="N">Microbial Sensitivity Tests</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D064307" MajorTopicYN="Y">Microbiota</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D016982" MajorTopicYN="N">Micrococcus luteus</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020636" MajorTopicYN="N">Pantoea</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010447" MajorTopicYN="N">Peptide Hydrolases</DescriptorName><QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D010641" MajorTopicYN="N">Phenotype</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D012336" MajorTopicYN="N">RNA, Ribosomal, 16S</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D020638" MajorTopicYN="N">Rahnella</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D017422" MajorTopicYN="N">Sequence Analysis, DNA</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D013210" MajorTopicYN="N">Staphylococcus</DescriptorName><QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName><QualifierName UI="Q000302" MajorTopicYN="Y">isolation & purification</QualifierName><QualifierName UI="Q000472" MajorTopicYN="N">pathogenicity</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D014774" MajorTopicYN="N">Virulence</DescriptorName></MeshHeading></MeshHeadingList></MedlineCitation><PubmedData><History><PubMedPubDate 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Demir</name><name sortKey="Sevim, Ali" sort="Sevim, Ali" uniqKey="Sevim A" first="Ali" last="Sevim">Ali Sevim</name><name sortKey="Sevim, Elif" sort="Sevim, Elif" uniqKey="Sevim E" first="Elif" last="Sevim">Elif Sevim</name></noCountry><country name="Turquie"><noRegion><name sortKey="Demirci, Meryem" sort="Demirci, Meryem" uniqKey="Demirci M" first="Meryem" last="Demirci">Meryem Demirci</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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