A bioinformatic approach to identify core genome difference between Salmonella Pullorum and Salmonella Enteritidis

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A bioinformatic approach to identify core genome difference between Salmonella Pullorum and Salmonella Enteritidis. / Fei, Xiao; Li, Qiuchun; Olsen, John Elmerdahl; Jiao, Xinan.

In: Infection, Genetics and Evolution, Vol. 85, 104446, 2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Fei, X, Li, Q, Olsen, JE & Jiao, X 2020, 'A bioinformatic approach to identify core genome difference between Salmonella Pullorum and Salmonella Enteritidis', Infection, Genetics and Evolution, vol. 85, 104446. https://doi.org/10.1016/j.meegid.2020.104446

APA

Fei, X., Li, Q., Olsen, J. E., & Jiao, X. (2020). A bioinformatic approach to identify core genome difference between Salmonella Pullorum and Salmonella Enteritidis. Infection, Genetics and Evolution, 85, [104446]. https://doi.org/10.1016/j.meegid.2020.104446

Vancouver

Fei X, Li Q, Olsen JE, Jiao X. A bioinformatic approach to identify core genome difference between Salmonella Pullorum and Salmonella Enteritidis. Infection, Genetics and Evolution. 2020;85. 104446. https://doi.org/10.1016/j.meegid.2020.104446

Author

Fei, Xiao ; Li, Qiuchun ; Olsen, John Elmerdahl ; Jiao, Xinan. / A bioinformatic approach to identify core genome difference between Salmonella Pullorum and Salmonella Enteritidis. In: Infection, Genetics and Evolution. 2020 ; Vol. 85.

Bibtex

@article{9a52350e3f784c2a8fc8832f998a5d44,
title = "A bioinformatic approach to identify core genome difference between Salmonella Pullorum and Salmonella Enteritidis",
abstract = "S. Pullorum and S. Enteritidis are closely related in genetic terms, but they show very different pathogenicity and host range. S. Enteritidis infects many different hosts, usually causing acute gastroenteritis, while S. Pullorum is restricted to avian, where it causes systemic disease in young animals. The reason why they differ in host range and pathogenicity is unknown. The core-genome denotes those genes that are present in all strains within a clade, and in the present work, an automated bioinformatics workflow was developed and applied to identify core-genome differences between these two serovars with the aim to identify genome features associated with host specificity of S. Pullorum. Results showed that S. Pullorum unique coding sequences (CDS) were mainly concentrated in three regions not present in S. Enteritidis, suggesting that such CDS were taken up probably during the separation of the two types from their common ancestor. One of the unique regions encoded Pathogenicity Islands 19 (SPI-19), which encodes a type VI secretion system (T6SS). Single-nucleotide polymorphism (SNP) analysis identified 1791 conserved SNPs in coding sequences between the two serovars, including several SNPs located in a type IV secretion system (T4SS). Analyzing of 100 bp regions upstream of coding sequences identified 443 conserved SNPs between the two serovars, including SNP variations in type III secretion system effector (T3SE). In conclusion, this analysis has identified genetic features encoding putative factors controlling host-specificity in S. Pullorum. The novel bioinformatic workflow and associated scripts can directly be applied to other bacteria to uncover the genome difference between clades.",
keywords = "Core-genome, Enteritidis, Host-specificity, Pullorum, Salmonella",
author = "Xiao Fei and Qiuchun Li and Olsen, {John Elmerdahl} and Xinan Jiao",
year = "2020",
doi = "10.1016/j.meegid.2020.104446",
language = "English",
volume = "85",
journal = "Infection, Genetics and Evolution",
issn = "1567-1348",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - A bioinformatic approach to identify core genome difference between Salmonella Pullorum and Salmonella Enteritidis

AU - Fei, Xiao

AU - Li, Qiuchun

AU - Olsen, John Elmerdahl

AU - Jiao, Xinan

PY - 2020

Y1 - 2020

N2 - S. Pullorum and S. Enteritidis are closely related in genetic terms, but they show very different pathogenicity and host range. S. Enteritidis infects many different hosts, usually causing acute gastroenteritis, while S. Pullorum is restricted to avian, where it causes systemic disease in young animals. The reason why they differ in host range and pathogenicity is unknown. The core-genome denotes those genes that are present in all strains within a clade, and in the present work, an automated bioinformatics workflow was developed and applied to identify core-genome differences between these two serovars with the aim to identify genome features associated with host specificity of S. Pullorum. Results showed that S. Pullorum unique coding sequences (CDS) were mainly concentrated in three regions not present in S. Enteritidis, suggesting that such CDS were taken up probably during the separation of the two types from their common ancestor. One of the unique regions encoded Pathogenicity Islands 19 (SPI-19), which encodes a type VI secretion system (T6SS). Single-nucleotide polymorphism (SNP) analysis identified 1791 conserved SNPs in coding sequences between the two serovars, including several SNPs located in a type IV secretion system (T4SS). Analyzing of 100 bp regions upstream of coding sequences identified 443 conserved SNPs between the two serovars, including SNP variations in type III secretion system effector (T3SE). In conclusion, this analysis has identified genetic features encoding putative factors controlling host-specificity in S. Pullorum. The novel bioinformatic workflow and associated scripts can directly be applied to other bacteria to uncover the genome difference between clades.

AB - S. Pullorum and S. Enteritidis are closely related in genetic terms, but they show very different pathogenicity and host range. S. Enteritidis infects many different hosts, usually causing acute gastroenteritis, while S. Pullorum is restricted to avian, where it causes systemic disease in young animals. The reason why they differ in host range and pathogenicity is unknown. The core-genome denotes those genes that are present in all strains within a clade, and in the present work, an automated bioinformatics workflow was developed and applied to identify core-genome differences between these two serovars with the aim to identify genome features associated with host specificity of S. Pullorum. Results showed that S. Pullorum unique coding sequences (CDS) were mainly concentrated in three regions not present in S. Enteritidis, suggesting that such CDS were taken up probably during the separation of the two types from their common ancestor. One of the unique regions encoded Pathogenicity Islands 19 (SPI-19), which encodes a type VI secretion system (T6SS). Single-nucleotide polymorphism (SNP) analysis identified 1791 conserved SNPs in coding sequences between the two serovars, including several SNPs located in a type IV secretion system (T4SS). Analyzing of 100 bp regions upstream of coding sequences identified 443 conserved SNPs between the two serovars, including SNP variations in type III secretion system effector (T3SE). In conclusion, this analysis has identified genetic features encoding putative factors controlling host-specificity in S. Pullorum. The novel bioinformatic workflow and associated scripts can directly be applied to other bacteria to uncover the genome difference between clades.

KW - Core-genome

KW - Enteritidis

KW - Host-specificity

KW - Pullorum

KW - Salmonella

U2 - 10.1016/j.meegid.2020.104446

DO - 10.1016/j.meegid.2020.104446

M3 - Journal article

C2 - 32622081

AN - SCOPUS:85088218808

VL - 85

JO - Infection, Genetics and Evolution

JF - Infection, Genetics and Evolution

SN - 1567-1348

M1 - 104446

ER -

ID: 247496164