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Identification and Differentiation of Pseudomonas Species in Field Samples Using an rpoD Amplicon Sequencing Methodology.
Lauritsen, Jonas Greve; Hansen, Morten Lindqvist; Bech, Pernille Kjersgaard; Jelsbak, Lars; Gram, Lone; Strube, Mikael Lenz.
Afiliação
  • Lauritsen JG; Department of Biotechnology and Biomedicine, Technical University of Denmarkgrid.5170.3, Kongens Lyngby, Denmark.
  • Hansen ML; Department of Biotechnology and Biomedicine, Technical University of Denmarkgrid.5170.3, Kongens Lyngby, Denmark.
  • Bech PK; Department of Biotechnology and Biomedicine, Technical University of Denmarkgrid.5170.3, Kongens Lyngby, Denmark.
  • Jelsbak L; Department of Biotechnology and Biomedicine, Technical University of Denmarkgrid.5170.3, Kongens Lyngby, Denmark.
  • Gram L; Department of Biotechnology and Biomedicine, Technical University of Denmarkgrid.5170.3, Kongens Lyngby, Denmark.
  • Strube ML; Department of Biotechnology and Biomedicine, Technical University of Denmarkgrid.5170.3, Kongens Lyngby, Denmark.
mSystems ; 6(4): e0070421, 2021 Aug 31.
Article em En | MEDLINE | ID: mdl-34342531
ABSTRACT
Species of the genus Pseudomonas are used for several biotechnological purposes, including plant biocontrol and bioremediation. To exploit the Pseudomonas genus in environmental, agricultural, or industrial settings, the organisms must be profiled at the species level as their bioactivity potential differs markedly between species. Standard 16S rRNA gene amplicon profiling does not allow for accurate species differentiation. Thus, the purpose of this study was to develop an amplicon-based high-resolution method targeting a 760-nucleotide (nt) region of the rpoD gene enabling taxonomic differentiation of Pseudomonas species in soil samples. The method was benchmarked on a 16-member Pseudomonas species mock community. All 16 species were correctly and semiquantitatively identified using rpoD gene amplicons, whereas 16S rRNA V3-V4 amplicon sequencing only correctly identified one species. We analyzed the Pseudomonas profiles in 13 soil samples in northern Zealand, Denmark, where samples were collected from grassland (3 samples) and agriculture soil (10 samples). Pseudomonas species represented up to 0.7% of the 16S rRNA gene abundance, of which each sampling site contained a unique Pseudomonas composition. Thirty culturable Pseudomonas strains were isolated from each grassland site and 10 from each agriculture site and identified by Sanger sequencing of the rpoD gene. In all cases, the rpoD amplicon approach identified more species than were found by cultivation, including hard-to-culture nonfluorescent pseudomonads, as well as more than were found by 16S rRNA V3-V4 amplicon sequencing. Thus, rpoD profiling can be used for species profiling of Pseudomonas, and large-scale prospecting of bioactive Pseudomonas may be guided by initial screening using this method. IMPORTANCE A high-throughput sequencing-based method for profiling of Pseudomonas species in soil microbiomes was developed and identified more species than 16S rRNA gene sequencing or cultivation. Pseudomonas species are used as biocontrol organisms and plant growth-promoting agents, and the method will allow tracing of specific species of Pseudomonas as well as enable screening of environmental samples for further isolation and exploitation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: MSystems Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: MSystems Ano de publicação: 2021 Tipo de documento: Article