» Articles » PMID: 38313017

Resequencing and Characterization of the First Genome Isolated from Camel

Overview
Journal PeerJ
Date 2024 Feb 5
PMID 38313017
Authors
Affiliations
Soon will be listed here.
Abstract

Background: is a zoonotic Gram-positive bacterial pathogen known to cause different diseases in many mammals, including lymph node abscesses in camels. Strains from biovars equi and ovis of can infect camels. Comparative genomics could help to identify features related to host adaptation, and currently strain Cp162 from biovar equi is the only one from camel with a sequenced genome.

Methods: In this work, we compared the quality of three genome assemblies of strain Cp162 that used data from the DNA sequencing platforms SOLiD v3 Plus, IonTorrent PGM, and Illumina HiSeq 2500 with an optical map and investigate the unique features of this strain. For this purpose, we applied comparative genomic analysis on the different Cp162 genome assembly versions and included other 129 genomes from the same species.

Results: Since the first version of the genome, there was an increase of 88 Kbp and 121 protein-coding sequences, a decrease of pseudogenes from 139 to 53, and two inversions and one rearrangement corrected. We identified 30 virulence genes, none associated to the camel host, and the genes and predicted to confer resistance to rifampin. In comparison to 129 genomes of the same species, strain Cp162 has four genes exclusively present, two of them code transposases and two truncated proteins, and the three exclusively absent genes , NUDIX domain protein, and Hypothetical protein. All 130 genomes had the rifampin resistance genes and . Our results found no unique gene that could be associated with tropism to camel host, and further studies should include more genomes and genome-wide association studies testing for genes and SNPs.

Citing Articles

First comparative genomics analysis of Corynebacterium auriscanis.

Vinhal A, de Araujo M, Rodrigues E, Castro D, Pereira C, Custodio D Mem Inst Oswaldo Cruz. 2024; 119:e240156.

PMID: 39476150 PMC: 11508509. DOI: 10.1590/0074-02760240156.


Corynebacterium pseudotuberculosis: Whole genome sequencing reveals unforeseen and relevant genetic diversity in this pathogen.

Hiller E, Horz V, Sting R PLoS One. 2024; 19(8):e0309282.

PMID: 39186721 PMC: 11346948. DOI: 10.1371/journal.pone.0309282.

References
1.
Mascher M, Stein N . Genetic anchoring of whole-genome shotgun assemblies. Front Genet. 2014; 5:208. PMC: 4083584. DOI: 10.3389/fgene.2014.00208. View

2.
Sereika M, Kirkegaard R, Karst S, Michaelsen T, Sorensen E, Wollenberg R . Oxford Nanopore R10.4 long-read sequencing enables the generation of near-finished bacterial genomes from pure cultures and metagenomes without short-read or reference polishing. Nat Methods. 2022; 19(7):823-826. PMC: 9262707. DOI: 10.1038/s41592-022-01539-7. View

3.
Tettelin H, Masignani V, Cieslewicz M, Donati C, Medini D, Ward N . Genome analysis of multiple pathogenic isolates of Streptococcus agalactiae: implications for the microbial "pan-genome". Proc Natl Acad Sci U S A. 2005; 102(39):13950-5. PMC: 1216834. DOI: 10.1073/pnas.0506758102. View

4.
Lehri B, Seddon A, Karlyshev A . The hidden perils of read mapping as a quality assessment tool in genome sequencing. Sci Rep. 2017; 7:43149. PMC: 5320493. DOI: 10.1038/srep43149. View

5.
Hassan S, Schneider M, Ramos R, Carneiro A, Ranieri A, Guimaraes L . Whole-genome sequence of Corynebacterium pseudotuberculosis strain Cp162, isolated from camel. J Bacteriol. 2012; 194(20):5718-9. PMC: 3458653. DOI: 10.1128/JB.01373-12. View