Moss Timothy J M, Knox Christine L, Kallapur Suhas G, Nitsos Ilias, Theodoropoulos Christina, Newnham John P, Ikegami Machiko, Jobe Alan H
School of Women's and Infants' Health, Faculty of Medicine, Dentistry, and Health Sciences, University of Western Australia, Perth, Western Australia, Australia.
Am J Obstet Gynecol. 2008 Jan;198(1):122.e1-8. doi: 10.1016/j.ajog.2007.06.065.
The objective of the study was to determine the effects in late gestation of Ureaplasma parvum serovar 3 colonization and the effects, preterm, of U. parvum serovar 6.
Ewes received an intraamniotic (i.a.) injection of U. parvum serovar 6 (20 x 10(6) colony-forming units [cfu]; n = 9), U. parvum serovar 3 (20 x 10(3) cfu; n = 6), vehicle (n = 10), or saline (n = 4) on day 80 of pregnancy (d). The lambs were delivered at 125 d (U. parvum serovar 6, n = 9; saline or media controls, n = 9) or 145 d (U. parvum serovar 3, n = 6; media controls, n = 5) for assessment of inflammation and lung maturation.
I.a. ureaplasmas caused histologic chorioamnionitis but not preterm delivery. Fetal lung epithelium was colonized with ureaplasmas at both gestational ages, and pulmonary interleukin-8 levels had doubled in the ureaplasma-colonized animals, compared with the controls at 145 d. Surfactant levels in bronchoalveolar lavage fluid had increased 8-fold and 2.5-fold at 125 and 145 d, respectively, after ureaplasma injection.
Fetal lung inflammation and altered development accompanies ureaplasma colonization, regardless of age at delivery.
本研究的目的是确定微小脲原体血清型3在妊娠晚期定植的影响以及微小脲原体血清型6对早产的影响。
在妊娠第80天,母羊接受羊膜腔内注射微小脲原体血清型6(20×10⁶菌落形成单位[cfu];n = 9)、微小脲原体血清型3(20×10³ cfu;n = 6)、赋形剂(n = 10)或生理盐水(n = 4)。羔羊在125天(微小脲原体血清型6,n = 9;生理盐水或培养基对照,n = 9)或145天(微小脲原体血清型3,n = 6;培养基对照,n = 5)分娩,以评估炎症和肺成熟情况。
羊膜腔内注射脲原体引起组织学绒毛膜羊膜炎,但未导致早产。在两个胎龄时,胎儿肺上皮均被脲原体定植,与145天时的对照组相比,脲原体定植动物的肺白细胞介素-8水平增加了一倍。注射脲原体后,支气管肺泡灌洗液中的表面活性剂水平在125天和145天时分别增加了8倍和2.5倍。
无论分娩时的胎龄如何,胎儿肺部炎症和发育改变均伴随脲原体定植。