[4] Among its 544 predicted protein-coding genes are several that are usually restricted to cellular organisms, such as translation factors and enzymes for DNA repair and carbohydrate synthesis.
The virus packages several distinct groups of proteins, including a presumably complete base excision repair (BER) pathway.
[8] Mature CroV consists of a 300 nm diameter outer protein shell with icosahedral symmetry, an underlying lipid membrane, and an inner core that contains the genome.
[citation needed] CroV is the sole member of the genus Cafeteriavirus in the family Mimiviridae within the proposed order Megavirales.
Acanthamoeba polyphaga mimivirus is its closest known relative, although the two viruses share less than one-third of homologous genes.
Due to production of transcriptional genes, like that of tRNA synthetase, the virus is able to modify and regulate host translational machinery that results in CroV being less dependent on host-cell components.
The presence and expression of 10 genes involved in glycoprotein synthesis were identified, suggesting that CroV is able to potentially partake in virion-cell recognition.
It encodes an entire biosynthetic pathway for the creation of 3-Deoxy-D-manno-oct-2-ulosonic acid, or KDO, which is a component of the cell walls of gram-negative bacteria.
When there are low numbers of Cafeteria roenbergensis due to extensive CroV infections, the bacterial populations rise exponentially.