TY - JOUR
T1 - Strengthening the genomic surveillance of Francisella tularensis by using culture-free whole-genome sequencing from biological samples
AU - Isidro, Joana
AU - Escudero, Raquel
AU - Luque-Larena, Juan José
AU - Pinto, Miguel
AU - Borges, Vítor
AU - González-Martín-Niño, Rosa
AU - Duarte, Sílvia
AU - Vieira, Luís
AU - Mougeot, François
AU - Vidal, Dolors
AU - Herrera-Rodríguez, Daniel
AU - Rodríguez-Pastor, Ruth
AU - Herrero-Cófreces, Silvia
AU - Jubete-Tazo, Fernando
AU - Gomes, João Paulo
AU - Lopes de Carvalho, Isabel
N1 - Publisher Copyright:
Copyright © 2024 Isidro, Escudero, Luque-Larena, Pinto, Borges, González-Martín-Niño, Duarte, Vieira, Mougeot, Vidal, Herrera-Rodríguez, Rodríguez-Pastor, Herrero-Cófreces, Jubete-Tazo, Gomes and Lopes de Carvalho.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Introduction: Francisella tularensis is a highly infectious bacterium that causes the zoonotic disease tularemia. The development of genotyping methods, especially those based on whole-genome sequencing (WGS), has recently increased the knowledge on the epidemiology of this disease. However, due to the difficulties associated with the growth and isolation of this fastidious pathogen in culture, the availability of strains and subsequently WGS data is still limited. Methods: To surpass these constraints, we aimed to implement a culture-free approach to capture and sequence F. tularensis genomes directly from complex samples. Biological samples obtained from 50 common voles and 13 Iberian hares collected in Spain were confirmed as positive for F. tularensis subsp. holarctica and subjected to a WGS target capture and enrichment protocol, using RNA oligonucleotide baits designed to cover F. tularensis genomic diversity. Results: We obtained full genome sequences of F. tularensis from 13 animals (20.6%), two of which had mixed infections with distinct genotypes, and achieved a higher success rate when compared with culture-dependent WGS (only successful for two animals). The new genomes belonged to different clades commonly identified in Europe (B.49, B.51 and B.262) and subclades. Despite being phylogenetically closely related to other genomes from Spain, the detected clusters were often found in other countries. A comprehensive phylogenetic analysis, integrating 599 F. tularensis subsp. holarctica genomes, showed that most (sub)clades are found in both humans and animals and that closely related strains are found in different, and often geographically distant, countries. Discussion: Overall, we show that the implemented culture-free WGS methodology yields timely, complete and high-quality genomic data of F. tularensis, being a highly valuable approach to promote and potentiate the genomic surveillance of F. tularensis and ultimately increase the knowledge on the genomics, ecology and epidemiology of this highly infectious pathogen.
AB - Introduction: Francisella tularensis is a highly infectious bacterium that causes the zoonotic disease tularemia. The development of genotyping methods, especially those based on whole-genome sequencing (WGS), has recently increased the knowledge on the epidemiology of this disease. However, due to the difficulties associated with the growth and isolation of this fastidious pathogen in culture, the availability of strains and subsequently WGS data is still limited. Methods: To surpass these constraints, we aimed to implement a culture-free approach to capture and sequence F. tularensis genomes directly from complex samples. Biological samples obtained from 50 common voles and 13 Iberian hares collected in Spain were confirmed as positive for F. tularensis subsp. holarctica and subjected to a WGS target capture and enrichment protocol, using RNA oligonucleotide baits designed to cover F. tularensis genomic diversity. Results: We obtained full genome sequences of F. tularensis from 13 animals (20.6%), two of which had mixed infections with distinct genotypes, and achieved a higher success rate when compared with culture-dependent WGS (only successful for two animals). The new genomes belonged to different clades commonly identified in Europe (B.49, B.51 and B.262) and subclades. Despite being phylogenetically closely related to other genomes from Spain, the detected clusters were often found in other countries. A comprehensive phylogenetic analysis, integrating 599 F. tularensis subsp. holarctica genomes, showed that most (sub)clades are found in both humans and animals and that closely related strains are found in different, and often geographically distant, countries. Discussion: Overall, we show that the implemented culture-free WGS methodology yields timely, complete and high-quality genomic data of F. tularensis, being a highly valuable approach to promote and potentiate the genomic surveillance of F. tularensis and ultimately increase the knowledge on the genomics, ecology and epidemiology of this highly infectious pathogen.
KW - Francisella tularensis
KW - Microtus arvalis
KW - RNA oligonucleotide baits
KW - SureSelect
KW - WGS
UR - http://www.scopus.com/inward/record.url?scp=85185109642&partnerID=8YFLogxK
U2 - 10.3389/fmicb.2023.1277468
DO - 10.3389/fmicb.2023.1277468
M3 - Article
C2 - 38249473
AN - SCOPUS:85185109642
SN - 1664-302X
VL - 14
JO - Frontiers in Microbiology
JF - Frontiers in Microbiology
M1 - 1277468
ER -