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Draft Genome Sequence of Novel Candidatus Ornithobacterium hominis Carrying Antimicrobial Resistance Genes in Egypt

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Abstract Background Candidatus Ornithobacterium hominis (O. hominis), which was found in Egyptian nasopharyngeal swabs but remains unidentified, has been associated with respiratory disorders in humans. Herein, we presented two draft genome assemblies of O. hominis that were extracted from metagenomic data using the Illumina sequencing method. The primary goal of this study was to present the first O. hominis genome sequence from Egyptian populations. Results The genome size was estimated to be 1,931,660 base pairs (bp), with 1,837 predicted coding regions and a G + C content of 35.62%. The toxA gene, 20 antibiotic resistance genes, and gliding motility genes were found in the genome assembly. Gliding motility lipoproteins (GldD, GldJ, GldN, and GldH) and the gliding motility-associated ABC transporter substrate-binding protein, which acts as a crucial virulence mechanism in Flavobacterium species, were identified. The genome contained unique proteins, such as the ParE1 toxin, that exhibit a defense mechanism against quinolone and other antibiotic actions. The cobalt-zinc-cadmium resistance protein CzcB, which is necessary for metal resistance, urease regulation, and colonization, was also detected. Several multidrug resistance proteins were identified, such as MexB, mdtK, yheI, and VanC. Conclusion Numerous virulence factors such as toxA and gliding motility genes, were present in the core O. hominis genome. Additionally, the draft genome contains several antibiotic-resistance genes. These findings may contribute to a better understanding of the genomic landscape of O. hominis and the identification of genes involved in virulence and antibiotic resistance.
Title: Draft Genome Sequence of Novel Candidatus Ornithobacterium hominis Carrying Antimicrobial Resistance Genes in Egypt
Description:
Abstract Background Candidatus Ornithobacterium hominis (O.
hominis), which was found in Egyptian nasopharyngeal swabs but remains unidentified, has been associated with respiratory disorders in humans.
Herein, we presented two draft genome assemblies of O.
hominis that were extracted from metagenomic data using the Illumina sequencing method.
The primary goal of this study was to present the first O.
hominis genome sequence from Egyptian populations.
Results The genome size was estimated to be 1,931,660 base pairs (bp), with 1,837 predicted coding regions and a G + C content of 35.
62%.
The toxA gene, 20 antibiotic resistance genes, and gliding motility genes were found in the genome assembly.
Gliding motility lipoproteins (GldD, GldJ, GldN, and GldH) and the gliding motility-associated ABC transporter substrate-binding protein, which acts as a crucial virulence mechanism in Flavobacterium species, were identified.
The genome contained unique proteins, such as the ParE1 toxin, that exhibit a defense mechanism against quinolone and other antibiotic actions.
The cobalt-zinc-cadmium resistance protein CzcB, which is necessary for metal resistance, urease regulation, and colonization, was also detected.
Several multidrug resistance proteins were identified, such as MexB, mdtK, yheI, and VanC.
Conclusion Numerous virulence factors such as toxA and gliding motility genes, were present in the core O.
hominis genome.
Additionally, the draft genome contains several antibiotic-resistance genes.
These findings may contribute to a better understanding of the genomic landscape of O.
hominis and the identification of genes involved in virulence and antibiotic resistance.

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