Survey of the Endophytic Bacteria Inhabiting Wild
            <i>Daucus</i>
            Seed Using 16S rRNA Gene Amplicon Sequencing

Kumar, Shiv; Johnson, Linda J.; Teasdale, Suliana; Morozova, Yulia; Bonth, Anouck C. M. de; Jáuregui, Ruy; Hannaford, Rina; Card, Stuart D.

doi:10.1128/mra.00140-23

Cited by 4 publications

(1 citation statement)

References 12 publications

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“…Using these primers, the authors reported a very low abundance of plant DNA amplification following quantitative PCR (qPCR) analysis. Similarly, Kumar et al (2023) reported only low levels of amplification of plant chloroplast DNA using 335F/769R for carrot seed microbiota analysis. However, in our study, 15% of reads from the shoot bacterial data set were attributed to plant DNA when using the 335F/769R primer pair.…”

Section: Reducing Plant Organelle Dna Amplificationmentioning

confidence: 99%

Evaluation of 16S rRNA gene primer pairs for bacterial community profiling in an across soil and ryegrass plant study

Shi,

Kumar,

Young

et al. 2023

J of Sust Agri & Env

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IntroductionAs microbes play important roles in many hosts and niches, linking microbiota across niches is becoming an important area of research. Studying microbiota across multiple niches would allow understanding of ecosystem‐level interactions and potential points of better manipulation for agriculture gains. However, a suitable methodology to characterize microbiota from vast different niches is currently lacking. We used the plant shoot and soil as two important niches for this case study.Materials and MethodsConsidering the important linkage plant play in connecting above‐ and below‐ground ecosystems and challenges of working with plant microbiota, we first compared three commonly used 16S ribosomal RNA gene primer pairs targeting V3–V4 or V5–V7 regions coupled with Illumina sequencing for bacterial communities associated with ryegrass shoot. Then the selected primer was used to amplify bacterial communities in soil and rhizosphere samples for comparison with the commonly used 338F/806R. Finally, core operational taxonomic units (OTUs) across soil and plant niches were identified.ResultsPrimer pair 799F/1193R amplified the lowest number of plant organelle sequences (<0.2% of total sequences) and consistently showed the highest α‐diversity compared with 338F/806R and 335F/769R. For soil and rhizosphere samples, 799F/1193R also demonstrated significantly higher α‐diversity indices compared with 338F/806R. The bacterial phyla commonly detected by both primer pairs comprised >97% of the total relative abundance in soil and rhizosphere samples. In addition, the differences in bacterial communities of the soil and rhizosphere samples were more evident when using 799F/1193R than 338F/806R. Using the 799F/1193R data set, 50 core bacterial OTUs were identified across soil, rhizosphere and shoot niches, whereas only 38 core OTUs were identified when using 338F/806R. Most of these core OTUs were dominant in either shoot or soil niche.ConclusionPrimer pair 799F/1193R is suitable for bacterial community studies targeting ryegrass plant and soil microbiota, in particular for cross‐niches studies.

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Section: Reducing Plant Organelle Dna Amplificationmentioning

confidence: 99%