Real-time PCR method to quantify Sp245 strain of Azospirillum baldaniorum on Brachiaria grasses under field conditions

Purpose Bacterial quantification by qPCR is considered the gold standard for microbial molecular diagnosis. However, a fundamental pre-requisite in this methodology is the designing of specific primers for the bacterium of interest. With the increase in bacterial genome sequencing data in the recent...

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Bibliographic Details
Published in:Plant and soil 2021-11, Vol.468 (1-2), p.525-538
Main Authors: Soares, Isis Capella, Pacheco, Rafael Sanches, da Silva, Cleudison Gabriel Nascimento, Santos, Rafael Salazar, Baldani, Jose Ivo, Urquiaga, Segundo, Vidal, Marcia Soares, Simoes-Araujo, Jean Luiz
Format: Article
Language:English
Subjects:
Agriculture
Azospirillum
Bacteria
Biomedical and Life Sciences
Brachiaria
Cultivars
Ecology
Environmental aspects
Field tests
Gene sequencing
Genetic aspects
Genomes
Grasses
Inoculation
Life Sciences
Methods Paper
Microorganisms
Nucleotide sequence
Physiological aspects
Plant Physiology
Plant Sciences
Polymerase chain reaction
Primers
Proteobacteria
Real time
Shoots
Soil Science & Conservation
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Summary:Purpose Bacterial quantification by qPCR is considered the gold standard for microbial molecular diagnosis. However, a fundamental pre-requisite in this methodology is the designing of specific primers for the bacterium of interest. With the increase in bacterial genome sequencing data in the recent years, it has become possible to design specific primers that can be used to quantify different strains of the same bacterial species. Methods To develop a real-time PCR (qPCR) protocol for the specific quantification of Azospirillum baldaniorum Sp245 strain (old Azospirillum brasilense ), the Sp245 genome sequence was fragmented into small contigs with 500 base pairs each, and analyzed for similarity against the NCBI non-redundant database. A. baldaniorum- specific contigs were used to design the primers. The best pair of primers was used to quantify these bacteria after inoculation in different cultivars of Brachiaria , grown under field conditions. Results Our results showed that the primer pair Sp245p10 was highly specific for the Sp245 strain in the Brachiaria root and shoot field under different conditions. The qPCR assay using these primers showed differences among cultivars in the number of bacteria detected in plants after inoculation. Additionally, the number of bacteria observed in the roots was higher than that in the shoots. Conclusion The qPCR methodology using a Sp245 strain-specific primer may be used to monitor A. baldaniorum inoculated into other plants and may find potential application in field experiments.
ISSN:0032-079X
1573-5036
DOI:10.1007/s11104-021-05137-y