Cardiobacterium hominis
Cardiobacterium hominis /ˌkɑːrdiəʊbækˈtɪəriəm ˈhɒmɪnɪs/ is a microaerophilic, pleomorphic, fastidious, Gram-negative bacterium part of the Cardiobacteriaceae family and the HACEK group. It is most commonly found in the human microbiota, specifically the oropharyngeal region including the mouth and upper part of the respiratory tract. It is one of the causes of endocarditis, a life-threatening inflammation close to the heart's inner lining and valves. While infections caused by Cardiobacterium hominis are uncommon, various clinical manifestations are linked to the bacterium, including meningitis, sepsis, and bone infections.
Etymology
In 1964, researchers I. J. Slotnick and Mary Dougherty named the species after their research on a 54-year-old male patient. The genus Cardiobacterium is a phrase combined with two foreign words, kardia and bacterium. The feminine noun "kardia" translates to heart, and the Latin neuter noun "bacterium" has a meaning of small rod. Hominis is a Latin genitive masculine noun which is translated as human being, of a man. The full genus and species can be translated into English as a bacterium of the heart of a human being, reflecting the original isolation that occurred from the Infective endocarditis in the heart valves.Discovery
Cardiobacterium hominis was originally discovered in 1962 based on analysis of four cases of Infective endocarditis over ten months. Upon its first isolation, researchers described Cardiobacterium hominis, which was unrecognized then, as a Pasteurella-like organism and categorized as group "II-D" by the Centers for Disease Control and Prevention.In 1964, researchers I. J. Slotnick and M. Dougherty from the Laboratory of Bacteriology, St. Jude Hospital and Department of Microbiology, University of Tennessee found Cardiobacterium hominis in a 54-year-old male patient with infective endocarditis. Surgeons found a large hole in the aortic valve, and the researchers later cultured the aortic tissue. Gram-negative bacteria with a rod morphology were isolated from the tissue after 48 hours. Cardiobacterium hominis was later identified using mass spectroscopy. Incidentally, the bacteria was later characterized to be another species in the genus Cardiobacterium, because it was found in cardiac tissue and found to be a cause of infective endocarditis. Identifying this bacterium proved to be challenging because of its pleomorphic nature. Cardiobacterium hominis was classified into the HACEK group because of its similar infectious profile to the rest of the HACEK organisms, such as genera groups, Haemophilus, Aggregatibacter, Eikenella, and Kingella, which have all been known to cause endocarditis in humans.
Taxonomy
Cardiobacterium hominis belongs to the domain Bacteria and phylum Pseudomonadota. The organism is a member of class Gammaproteobacteria, order Cardiobacteriales, family Cardiobacteriaceae, and genus Cardiobacterium. The only other species of the Cardiobacterium genus is Cardiobacterium valvarum, known for the oropharyngeal flora and similar causative organism to infective endocarditis. Therefore, Cardiobacterium valvarum is the organism's closest phylogenetic neighbor. The next closest neighbors to the bacteria are in the family of Pseudomonadota, which are commonly referred to as proteobacteria. Some Gram-negative bacteria that are in this phylum are Escherichia, Salmonella, and Vibrio.Genomics
Genomic DNA was extracted using the Wizard genomic DNA purification kit from the company Promega. DNA sequencing produced 150-bp paired-end reads, with reads shorter than 150 bp disregarded. Assembly was performed by SPAdes genome assembler using different k-mer values from 43-127 and Quast using N50 and L50 scores and the lowest quantity of contigs greater than 1000 bp. Annotation of these assemblies was done using RSAT and analyzed using SEED viewer. Searching for antibiotic resistance genes and prophage sequences were completed via PHAST while identification, using a method that compared translated coding sequences and proteins that correspond to them, was done using the CLUSTAL-W database. It was found after sequencing 2,456,795 15-bp paired-end reads and assembling them, it was found that the RAST system predicted 2,489 CoDing Sequences CDSs with some of the functions being cell wall metabolism, virulence and defense, carbohydrate metabolism, protein metabolism, RNA metabolism, lipid metabolism, and DNA metabolism. After further annotation, some CDSs revealed potential function involved in antibiotic resistance but Resfinder demonstrated a higher sensitivity to antibiotics such as ceftriaxone and gentamicin. Lastly, one complete and two incomplete prophage sequences appeared as well.DNA sequencing produced 150-bp paired-end reads, with reads shorter than 150-bp disregarded. Annotation of assemblies was done using RAST and analyzed using SEED viewer. Searching of antibiotic resistance genes and prophage sequences was completed via PHAST while identification, using a method that compared translated coding sequences and proteins that are correspondent to them, was done using the CLUSTAL-W database.
Overall, the sequenced T05791 strain of Cardiobacterium hominis was found to have one circular chromosome with a genome size of 2.7 Megabases and a G+C content of 59%. The assembly level is a complete genome consisting over around 2670755 nucleotides and a total gene count of 2474, 2412 being protein genes and 42 being RNA genes. The RAST system predicted genes encoding for functions such as cell wall metabolism, defense, carbohydrate metabolism, protein metabolism, RNA metabolism, lipid metabolism, and DNA metabolism In regards to its pathogenicity, Cardiobacterium hominis has very low virulence and minimal genes aid in its pathogenic abilities. Further annotation revealed potential functions involved in antibiotic resistance, but Resfinder demonstrated a higher sensitivity to antibiotics such as ceftriaxone and gentamicin. One complete and two incomplete prophage sequences appeared as well.