Automating high-throughput screening for anthracnose resistance in common bean using allele specific PCR

Marysia Zaleski-Cox; Phillip N Miklas; Alvaro Soler-Garzón; Valerio Hoyos-Villegas

doi:10.1186/s13007-023-01071-5

Automating high-throughput screening for anthracnose resistance in common bean using allele specific PCR

Plant Methods. 2023 Oct 3;19(1):102. doi: 10.1186/s13007-023-01071-5.

Authors

Marysia Zaleski-Cox¹, Phillip N Miklas², Alvaro Soler-Garzón³, Valerio Hoyos-Villegas⁴

Affiliations

¹ Department of Plant Science, McGill University, Montreal, QC, Canada.
² Grain Legume Genetics and Physiology Research Unit, USDA-ARS, Prosser, WA, USA.
³ Irrigated Agriculture Research and Extension Center, Washington State University, Prosser, WA, USA.
⁴ Department of Plant Science, McGill University, Montreal, QC, Canada. valerio.hoyos-villegas@mcgill.ca.

Abstract

Background: Common beans (Phaseolus vulgaris L.) provide important protein and calories globally. Anthracnose (Colletotrichum lindemuthianum (Sacc. & Magnus) Briosi & Cavara, 1889) is a major disease in common bean and causes significant yield losses in bean production areas. Screening for markers linked to known disease resistance genes provides useful information for plant breeders to develop improved common bean varieties. The Kompetitive Allele Specific PCR (KASP) assay is an affordable genetic screening technique that can be used to accelerate breeding programs, but manual DNA extraction and KASP assay preparation are time-consuming. Several KASP markers have been developed for genes involved in resistance to bean anthracnose, which can reduce yield by up to 100%, but their usefulness is hindered by the labor required to screen a significant number of bean lines. Our research objective was to develop publicly available protocols for DNA extraction and KASP assaying using a liquid handling robot (LHR) which would facilitate high-throughput genetic screening with less active human time required. Anthracnose resistance markers were used to compare manual and automated results.

Results: The 12 bean anthracnose differential cultivars were screened for four anthracnose KASP markers linked to the resistance genes Co-1, Co-3 and Co-4² both by hand and with the use of an LHR. A protocol was written for DNA extraction and KASP assay thermocycling to implement the LHR. The LHR protocol reduced the active human screening time of 24 samples from 3h44 to 1h23. KASP calls were consistent across replicates but not always accurate for their known linked resistance genes, suggesting more specific markers still need to be developed. Using an LHR, information from KASP assays can be accumulated with little active human time.

Conclusion: Results suggest that LHRs can be used to expedite time-consuming and tedious lab work such as DNA extraction or PCR plate filling. Notably, LHRs can be used to prepare KASP assays for large sample sizes, facilitating higher throughput use of genetic marker screening tools.

Keywords: Anthracnose; High-throughput genotyping; KASP assay; Lab automation; Marker-assisted selection; Phaseolus vulgaris.

Grants and funding

322853/Fonds de recherche du Québec - Nature et technologies