Nelson S, Matlow A, Johnson G, Th'ng C, Dunn M, Quinn P
Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, The University of Toronto, Canada.
J Clin Microbiol. 1998 May;36(5):1236-9. doi: 10.1128/JCM.36.5.1236-1239.1998.
A PCR-based test was optimized for the detection of Ureaplasma urealyticum from neonatal respiratory specimens, with primers directed against the multiple-banded antigen gene (L. J. Teng, X. Zheng, J. I. Glass, H. Watson, J. Tsai, and G. H. Cassell, J. Clin. Microbiol. 32:1464-1469, 1994). Endotracheal tube aspirates (225) from 103 low-birth-weight neonates (<1,250 g) were taken, when possible, at days 0, 4, and 14 after birth and examined by culture and by PCR. Of 77 specimens positive by either method, 73 were detected by PCR and 60 were detected by culture. Overall, 36% of the neonates were positive for U. urealyticum by either method. Of 16 patients with PCR-positive-culture-negative results, 13 had positive cultures at another sampling point, and one additional patient had a twin with positive cultures. Of 11 patients with day 0 specimens positive by PCR alone, 9 subsequently became culture positive, demonstrating the utility of this test in early detection. Multiple serovars were present in over 50% of positive specimens, with serovars 3 and 14 in combination being most prevalent. The amplicon size generated from the specimen by PCR correctly predicted the biovars isolated in over 85% of positive specimens. Thus, this PCR test was valuable in allowing early detection of U. urealyticum in neonatal respiratory specimens, as well as in providing biovar information.
一种基于聚合酶链反应(PCR)的检测方法经过优化,用于从新生儿呼吸道标本中检测解脲脲原体,其引物针对多带抗原基因(L. J. 滕、X. 郑、J. I. 格拉斯、H. 沃森、J. 蔡和G. H. 卡塞尔,《临床微生物学杂志》32:1464 - 1469, 1994)。在可能的情况下,采集了103名低体重新生儿(<1250克)出生后第0天、第4天和第14天的气管内吸出物(225份),并通过培养和PCR进行检测。在两种方法检测为阳性的77份标本中,73份通过PCR检测到,60份通过培养检测到。总体而言,两种方法检测到36%的新生儿解脲脲原体呈阳性。在16例PCR阳性而培养阴性的患者中,13例在另一个采样点培养结果为阳性,另有1例患者的双胞胎培养结果为阳性。在11例仅第0天标本PCR阳性的患者中,9例随后培养结果转为阳性,证明了该检测方法在早期检测中的实用性。超过50%的阳性标本中存在多种血清型,血清型3和14组合最为常见。通过PCR从标本中产生的扩增子大小正确预测了超过85%阳性标本中分离出的生物变种。因此,这种PCR检测方法对于早期检测新生儿呼吸道标本中的解脲脲原体以及提供生物变种信息具有重要价值。