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先天性感染和机会性感染:脲原体属和人型支原体。

Congenital and opportunistic infections: Ureaplasma species and Mycoplasma hominis.

作者信息

Waites Ken B, Schelonka Robert L, Xiao Li, Grigsby Peta L, Novy Miles J

机构信息

Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35249, USA.

出版信息

Semin Fetal Neonatal Med. 2009 Aug;14(4):190-9. doi: 10.1016/j.siny.2008.11.009. Epub 2008 Dec 23.

Abstract

There is strong evidence from clinical and experimental animal studies that ureaplasmas can invade the amnionic sac and induce an inflammatory response resulting in chorioamnionitis, preterm labor and neonatal lung injury. The ability of Ureaplasma spp. and Mycoplasma hominis to cause pneumonia, bacteremia, and meningitis in newborns can no longer be questioned. The association of Ureaplasma spp. with bronchopulmonary dysplasia has been supported by the majority of observational studies, but proof of causality is still lacking. The availability of molecular diagnostic technologies has enabled the designation of the two Ureaplasma biovars as individual species, but additional work must be done to establish whether there is differential pathogenicity between the Ureaplasma spp. or among their respective serovars. Future investigations to prevent prematurity should be directed toward identification and localization of specific micro-organisms combined with targeted antibiotic trials to determine whether such interventions can improve long-term infant outcomes.

摘要

临床和实验动物研究有强有力的证据表明,脲原体可侵入羊膜囊并引发炎症反应,导致绒毛膜羊膜炎、早产和新生儿肺损伤。脲原体属和人型支原体在新生儿中引发肺炎、菌血症和脑膜炎的能力已不容置疑。大多数观察性研究支持脲原体属与支气管肺发育不良之间的关联,但仍缺乏因果关系的证据。分子诊断技术的出现使得两种脲原体生物变种被指定为独立的物种,但仍需开展更多工作来确定脲原体属之间或其各自血清型之间是否存在致病性差异。未来预防早产的研究应致力于特定微生物的识别和定位,并结合针对性抗生素试验,以确定此类干预措施是否能改善婴儿的长期预后。

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