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首页> 外文期刊>BMC Infectious Diseases >Molecular evidence of Ureaplasma urealyticum and Ureaplasma parvum colonization in preterm infants during respiratory distress syndrome
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Molecular evidence of Ureaplasma urealyticum and Ureaplasma parvum colonization in preterm infants during respiratory distress syndrome

机译:呼吸窘迫综合征期间早产儿解脲脲原体和细小支原体定植的分子证据

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Background Ureaplasma urealyticum and U. parvum have been associated with respiratory diseases in premature newborns, but their role in the pathogenesis of the respiratory distress syndrome (RDS) is unclear. The aim of this study was to detect, using molecular techniques, the role of Mycoplasma spp. and Ureaplasma spp. in respiratory secretion and blood specimens of preterm newborns with or without RDS and to evaluate the prevalence of perinatal U. urealyticum or U. parvum infection. The influence of chemotherapy on the clinical course was also evaluated. Methods Tracheal aspirate or nasopharingeal fluid samples from 50 preterm babies with (24) or without RDS (26) were analysed for detection of U. urealyticum and U. parvum by culture identification assay and PCR. Sequencing analysis of amplicons allowed us to verify the specificity of methods. Clarithromycin (10 mg kg-1 twice a day) was administered in ureaplasma-positive patients who presented clinical signs of RDS. Results 15/24 neonates with RDS (p U. urealyticum or U. parvum. Culture identification assay was positive in 5/50 newborns, three of which with RDS. Sequencing analyses confirmed the specificity of these methods. Association of patent ductus arteriosus with ureaplasma colonization was more statistically significant (p = 0.0004) in patients with RDS than in those without RDS. Conclusion Colonization of the lower respiratory tract by Ureaplasma spp. and particularly by U. parvum in preterm newborns was related to RDS. The routine use of molecular methods could be useful to screen candidate babies for etiologic therapy.
机译:背景技术解脲脲原体和细小U.um已经与早产儿的呼吸系统疾病有关,但它们在呼吸窘迫综合征(RDS)发病机理中的作用尚不清楚。这项研究的目的是使用分子技术检测支原体的作用。和Ureaplasma spp。在有或没有RDS的早产新生儿的呼吸道分泌物和血液样本中进行分析,以评估围产期解脲支原体或细小U.感染的患病率。还评估了化疗对临床过程的影响。方法采用培养鉴定法和PCR法,对50例有(24)或无RDS(26)的早产儿气管吸出物或鼻咽液进行分析,以检测解脲脲原体和细小U.parvum。扩增子的测序分析使我们能够验证方法的特异性。克拉霉素(每天两次10 mg kg -1 两次)用于出现RDS临床体征的脲原体阳性患者。结果15/24例RDS(解脲脲原体或小U. U.新生儿)的培养鉴定试验在5/50新生儿中为阳性,其中3例为RDS。测序分析证实了这些方法的特异性。动脉导管未闭与脲原体的关联结论RDS患者的定居率高于无RDS的患者(p = 0.0004)结论结论早产儿尿素原种特别是U. parvum对下呼吸道的定植与RDS有关。这些方法可能有助于筛查候选婴儿进行病因治疗。

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