Genome shuffling enables quantitative trait locus mapping in Bacillus subtilis

D Delyana P. Vasileva H Hari B. Chhetri L Leah H. Hochanadel J Jared C. Streich J John H. Lagergren M Matthew J. Lane A Apurv Mhatre O Oumar Sacko M Marco N. Allemann E Edanur Oksuz D Dana L. Carper (Biosciences Division) B Benjamin Rubino S Sadie Chitwood Z Zachary D. Schmitz D Dawn M. Klingeman P Paul E. Abraham (Biosciences Division, Oak Ridge National Laboratory) R Richard J. Giannone D Daniel A. Jacobson J Joshua K. Michener (Biosciences Division)

Abstract

Abstract Genetic mapping is a powerful tool for eukaryotic genetics that has only been applied to bacteria in limited circumstances. Quantitative trait locus (QTL) mapping generally relies on sexual recombination to break linkages between genes, yet bacteria rarely undergo sufficient homologous recombination to generate suitable mapping populations. In this work, we used iterative biparental genome shuffling by protoplast fusion in Bacillus subtilis to generate a population of bacteria with substantial random recombination throughout their genomes. Individual shuffled progeny were arrayed in well plates, resequenced, and characterized for a range of complex phenotypes, including spore germination and swarming motility. Genetic mapping of the resulting phenotypes identified high-confidence QTLs of moderate size (~15 kb), and these associations were validated through targeted genetic swaps. This B. subtilis QTL population can easily be used to map additional phenotypes and the general approach for QTL mapping is applicable to a wide range of Gram-positive and Gram-negative bacteria using diverse methods for genome-wide recombination.

Article Details

Volume / Issue Vol. 17, Issue 1
Published August 05, 2026
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (19)

D

Delyana P. Vasileva

H

Hari B. Chhetri

L

Leah H. Hochanadel

J

Jared C. Streich

J

John H. Lagergren

M

Matthew J. Lane

A

Apurv Mhatre

O

Oumar Sacko

M

Marco N. Allemann

E

Edanur Oksuz

D

Dana L. Carper

Biosciences Division

B

Benjamin Rubino

S

Sadie Chitwood

Z

Zachary D. Schmitz

D

Dawn M. Klingeman

P

Paul E. Abraham

Biosciences Division, Oak Ridge National Laboratory

R

Richard J. Giannone

D

Daniel A. Jacobson

J

Joshua K. Michener

Biosciences Division