Development and implementation of multilocus sequence typing to study the diversity of the yeast Kluyveromyces marxianus in Italian cheeses
Author
Tittarelli, FabriziaVarela, Javier A.
Gethins, Loughlin
STANTON, CATHERINE

Ross, R.P.
Suzzi, Giovanna
Grazia, Luigi
Tofalo, Rosanna
Morrissey, John P.
Date
2018-02-01
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Tittarelli F, Varela JA, Gethins L, Stanton C, Ross RP, Suzzi G, Grazia L, Tofalo R, Morrissey JP. Development and implementation of multilocus sequence typing to study the diversity of the yeast Kluyveromyces marxianus in Italian cheeses. Microb Genom. 2018 Feb;4(2):e000153. doi: 10.1099/mgen.0.000153. Epub 2018 Jan 18. PMID: 29345222; PMCID: PMC5857380.Abstract
The yeast Kluyveromyces marxianus possesses advantageous traits like rapid growth, GRAS (generally regarded as safe) status and thermotolerance that make it very suitable for diverse biotechnological applications. Although physiological studies demonstrate wide phenotypic variation within the species, there is only limited information available on the genetic diversity of K. marxianus. The aim of this work was to develop a multilocus sequence typing (MLST) method for K. marxianus to improve strain classification and selection. Analysis of housekeeping genes in a number of sequenced strains led to the selection of five genes, IPP1, TFC1, GPH1, GSY2 and SGA1, with sufficient polymorphic sites to allow MLST analysis. These loci were sequenced in an additional 76 strains and used to develop the MLST. This revealed wide diversity in the species and separation of the culture collection and wild strains into multiple distinct clades. Two subsets of strains that shared sources of origin were subjected to MLST and split decomposition analysis. The latter revealed evidence of recombination, indicating that this yeast undergoes mating in the wild. A public access web-based portal was established to allow expansion of the database and application of MLST to additional K. marxianus strains. This will aid understanding of the genetic diversity of the yeast and facilitate biotechnological exploitation.Funder
Teagasc Walsh Fellowship Programme; People Programme (Marie Curie Actions) of the European Union's Seventh Framework Programme FP7/2007-2013Grant Number
2013046; 606795ae974a485f413a2113503eed53cd6c53
https://doi.org/10.1099/mgen.0.000153
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