Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
For Someone, You Are the Whole World: Host-Specificity of Salmonella enterica. / Меркушова, А.В.; Шиков, Антон Евгеньевич; Нижников, Антон Александрович; Антонец, Кирилл Сергеевич.
в: International Journal of Molecular Sciences, Том 24, № 18, 13670, 05.09.2023.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - For Someone, You Are the Whole World: Host-Specificity of Salmonella enterica
AU - Меркушова, А.В.
AU - Шиков, Антон Евгеньевич
AU - Нижников, Антон Александрович
AU - Антонец, Кирилл Сергеевич
PY - 2023/9/5
Y1 - 2023/9/5
N2 - Salmonella enterica is a bacterial pathogen known to cause gastrointestinal infections in diverse hosts, including humans and animals. Despite extensive knowledge of virulence mechanisms, understanding the factors driving host specificity remains limited. In this study, we performed a comprehensive pangenome-wide analysis of S. enterica to identify potential loci determining preference towards certain hosts. We used a dataset of high-quality genome assemblies grouped into 300 reference clusters with a special focus on four host groups: humans, pigs, cattle, and birds. The reconstructed pangenome was shown to be open and enriched with the accessory component implying high genetic diversity. Notably, phylogenetic inferences did not correspond to the distribution of affected hosts, as large compact phylogenetic groups were absent. By performing a pangenome-wide association study, we identified potential host specificity determinants. These included multiple genes encoding proteins involved in distinct infection stages, e.g., secretion systems, surface structures, transporters, transcription regulators, etc. We also identified antibiotic resistance loci in host-adapted strains. Functional annotation corroborated the results obtained with significant enrichments related to stress response, antibiotic resistance, ion transport, and surface or extracellular localization. We suggested categorizing the revealed specificity factors into three main groups: pathogenesis, resistance to antibiotics, and propagation of mobile genetic elements (MGEs).
AB - Salmonella enterica is a bacterial pathogen known to cause gastrointestinal infections in diverse hosts, including humans and animals. Despite extensive knowledge of virulence mechanisms, understanding the factors driving host specificity remains limited. In this study, we performed a comprehensive pangenome-wide analysis of S. enterica to identify potential loci determining preference towards certain hosts. We used a dataset of high-quality genome assemblies grouped into 300 reference clusters with a special focus on four host groups: humans, pigs, cattle, and birds. The reconstructed pangenome was shown to be open and enriched with the accessory component implying high genetic diversity. Notably, phylogenetic inferences did not correspond to the distribution of affected hosts, as large compact phylogenetic groups were absent. By performing a pangenome-wide association study, we identified potential host specificity determinants. These included multiple genes encoding proteins involved in distinct infection stages, e.g., secretion systems, surface structures, transporters, transcription regulators, etc. We also identified antibiotic resistance loci in host-adapted strains. Functional annotation corroborated the results obtained with significant enrichments related to stress response, antibiotic resistance, ion transport, and surface or extracellular localization. We suggested categorizing the revealed specificity factors into three main groups: pathogenesis, resistance to antibiotics, and propagation of mobile genetic elements (MGEs).
KW - Animals
KW - Anti-Bacterial Agents
KW - Cattle
KW - Host Specificity
KW - Humans
KW - Ion Transport
KW - Phylogeny
KW - Salmonella enterica/genetics
KW - Swine
UR - https://www.mendeley.com/catalogue/cf23a2ea-be66-3d69-9d44-3ed537410b1a/
U2 - 10.3390/ijms241813670
DO - 10.3390/ijms241813670
M3 - Article
C2 - 37761974
VL - 24
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
SN - 1422-0067
IS - 18
M1 - 13670
ER -
ID: 113594160