Classification
''Ureaplasma spp''. are one of the smallest known clonal bacteria. They are closely related to mycoplasmas as they lack a peptidoglycan cell wall, metabolize cholesterol, and require urea for ATP synthesis. The Ureaplasma genus has 14Clinical relevance
The clinical implications concerning the pathogenicity of ''U. parvum'' have yet to be determined because of its recent establishment as a separate species from ''U. urealyticum''. Due to the species heterogeneity in ''Ureaplasma spp''. not being noted in clinical studies prior to their distinction from each other, it is possible that ''U. urealyticym'' is disproportionately overrepresented compared to ''U. parvum''. As a consequence, interpreting data on ''Ureaplasma parvum'' can be difficult since there are currently few studies that differentiate between the ''Ureaplasma spp''. Therefore, there is little substantial evidence that ''U. parvum'' causes any of the diseases that have been associated with ''U. urealyticym'', specifically inflammatory vulvovaginitis, male infertility and non-gonococcal urethritis (NGU), female urethritis and urethral pain syndrome, pelvic inflammatory disease, cervicitis, ectopic pregnancy, and female infertility. It is important for future studies to accurately differentiate between ''U. urealyticum'' and ''U. parvum'', as this will aid in the etiological analysis of NGU and other diseases. ''Ureaplasma spp''. lack a cell wall and are therefore resistant to antimicrobials that specifically attack the cell wall. For this reason, ''Ureaplasma spp.'' are particularly difficult to diagnose and eradicate, and unnecessary treatment can further encourage antimicrobial resistance. As a result, extensive testing and treatment of the ''Ureaplasma spp''. is not always recommended. Ureaplasma parvum is usually part of the normal genital flora. Rarely can it cause invasive infections such as genitourinary infections, septic arthritis, or meningitis.Commensalism
''Ureaplasma parvum'' is commensal in both males and females, where it attaches itself to the mucosal lining of the urogenital tract. Damage to mucosal linings results in the relocation of ''Ureaplasma spp''. to other physiological areas of the body, which can lead to infection and disease. ''U. parvum'' has been investigated as an opportunistic pathogen, however current studies question its contribution to urogenital infections. For example, a study conducted by Rumyantseva et al showed that in female patients with varying vaginal microflora, ''U. parvum'' was the most prevalent mycoplasma. In normal vaginal microflora, 43.5% of samples were ''U. Parvum'' positive. Bacterial vaginosis and aerobic vaginitis samples were 59.9% and 23.9% ''U. Parvum'' positive, respectively. This study supports the symbiotic considerations between vaginal microflora (primarily normal and bacterial vaginosis) and mycoplasma such as ''U. parvum.''Current studies: ''Ureaplasma parvum'' in males
''Ureaplasma parvum'' (and ''U. urealyticum'') have been linked to nongonococcal urethritis (NGU), but the ''Ureaplasma spp''. have also been found in many healthy men, allowing for considerable skepticism that the two are correlated. Similarly, links to prostatitis and infertility are difficult to establish due to its presence in control groups. In andrology studies, the presence of ''U. parvum'' in semen has been found to be significant. Various ''Ureaplasma spp.'' isolates have been detected in semen via polymerase chain reaction (PCR) and immunofluorescent antibody assay. In 36.6% of washed samples, ''U. parvum'' was present. Andrology studies surrounding ''U. parvum'' demonstrated that the bacteria can remain on the spermatozoa even after washing.Current studies: ''Ureaplasma parvum'' in females
Current research indicates that ''U. parvum'' infections can cause pregnancy complications. In pregnant women with an intra-amniotic infection, ''U. parvum'' is the most common bacterium found. ''Ureaplasma'' spp. generally causes a more severe inflammatory response than other microbial infections. These infections can lead to preterm birth, maternal and fetal inflammation, placental inflammation (chorioamnionitis), and neonatal mortality. One study found that amniotic inoculation with a clinically isolated ''U. parvum'' serovar 14 causes preterm birth in animal models, while serovar 3 causes a low rate of preterm birth but a higher rate of neonatal mortality. Studies are ongoing.References
{{Taxonbar, from=Q4006425 parvum