RRC ID 55051
著者 Fuwa K, Seki M, Hirata Y, Yanagihara I, Nakura Y, Takano C, Kuroda K, Hayakawa S.
タイトル Rapid and simple detection of Ureaplasma species from vaginal swab samples using a loop-mediated isothermal amplification method.
ジャーナル Am J Reprod Immunol
Abstract PROBLEM:Ureaplasma species occasionally cause chorioamnionitis and premature labor. We developed a novel assay employing a loop-mediated isothermal amplification (LAMP) method to detect Ureaplasma parvum and Ureaplasma urealyticum.
METHOD OF STUDY:Loop-mediated isothermal amplification primers were designed to amplify Ureaplasma-specific ureaseB genes. Four U. parvum strains, 5 U. urealyticum strains and 14 reference bacterial species were evaluated. Forty-six vaginal swab samples were analyzed by LAMP, culture, and PCR.
RESULTS:Our LAMP primers were specific to each species and had no cross-reaction. Of 46 clinical specimens, the sensitivity, specificity, and positive and negative predictive values of the LAMP method were 100% (12/12), 100% (34/34), 100% (12/12), and 100% (34/34), respectively, whereas those of PCR were 66.7% (8/12), 100% (34/34), 100% (8/8), and 89.5% (34/38), respectively, compared to culture-based detection.
CONCLUSION:The LAMP detection method outperformed the culture and PCR methods. Early detection enables appropriate antibiotic selection for improved prenatal outcomes.
巻・号 79(1)
公開日 2018-1-1
DOI 10.1111/aji.12771
PMID 29154392
MeSH Cell Culture Techniques Cells, Cultured Chorioamnionitis / diagnosis* Early Diagnosis Female Humans Nucleic Acid Amplification Techniques / methods* Polymerase Chain Reaction Predictive Value of Tests Pregnancy Sensitivity and Specificity Time Factors Ureaplasma / physiology* Ureaplasma Infections / diagnosis* Ureaplasma urealyticum / physiology* Vagina / physiology*
IF 3.091
引用数 2
リソース情報
一般微生物 JCM 1232 JCM 11026 JCM 12093 JCM 1669 JCM 20624