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微小脲原体在子宫内发生选择,导致基因多样的分离株定殖于胎羊的绒毛膜羊膜。

Ureaplasma parvum undergoes selection in utero resulting in genetically diverse isolates colonizing the chorioamnion of fetal sheep.

作者信息

Dando Samantha J, Nitsos Ilias, Polglase Graeme R, Newnham John P, Jobe Alan H, Knox Christine L

机构信息

Institute of Health and Biomedical Innovation, Faculty of Health, Queensland University of Technology, Brisbane, Queensland, Australia.

出版信息

Biol Reprod. 2014 Feb 13;90(2):27. doi: 10.1095/biolreprod.113.113456. Print 2014 Feb.

Abstract

Ureaplasmas are the microorganisms most frequently isolated from the amniotic fluid of pregnant women and can cause chronic intrauterine infections. These tiny bacteria are thought to undergo rapid evolution and exhibit a hypermutatable phenotype; however, little is known about how ureaplasmas respond to selective pressures in utero. Using an ovine model of chronic intraamniotic infection, we investigated if exposure of ureaplasmas to subinhibitory concentrations of erythromycin could induce phenotypic or genetic indicators of macrolide resistance. At 55 days gestation, 12 pregnant ewes received an intraamniotic injection of a nonclonal, clinical Ureaplasma parvum strain followed by (i) erythromycin treatment (intramuscularly, 30 mg/kg/day, n = 6) or (ii) saline (intramuscularly, n = 6) at 100 days gestation. Fetuses were then delivered surgically at 125 days gestation. Despite injecting the same inoculum into all the ewes, significant differences between amniotic fluid and chorioamnion ureaplasmas were detected following chronic intraamniotic infection. Numerous polymorphisms were observed in domain V of the 23S rRNA gene of ureaplasmas isolated from the chorioamnion (but not the amniotic fluid), resulting in a mosaiclike sequence. Chorioamnion isolates also harbored the macrolide resistance genes erm(B) and msr(D) and were associated with variable roxithromycin minimum inhibitory concentrations. Remarkably, this variability occurred independently of exposure of ureaplasmas to erythromycin, suggesting that low-level erythromycin exposure does not induce ureaplasmal macrolide resistance in utero. Rather, the significant differences observed between amniotic fluid and chorioamnion ureaplasmas suggest that different anatomical sites may select for ureaplasma subtypes within nonclonal, clinical strains. This may have implications for the treatment of intrauterine ureaplasma infections.

摘要

解脲脲原体是最常从孕妇羊水中分离出的微生物,可引起慢性宫内感染。这些微小细菌被认为会经历快速进化并表现出超突变表型;然而,关于解脲脲原体如何应对子宫内的选择压力知之甚少。我们使用慢性羊膜腔内感染的绵羊模型,研究了解脲脲原体暴露于亚抑制浓度的红霉素是否会诱导大环内酯类耐药的表型或遗传指标。在妊娠55天时,12只怀孕母羊接受羊膜腔内注射非克隆临床微小脲原体菌株,随后在妊娠100天时进行(i)红霉素治疗(肌肉注射,30mg/kg/天,n = 6)或(ii)生理盐水(肌肉注射,n = 6)。然后在妊娠125天时通过手术分娩胎儿。尽管向所有母羊注射了相同的接种物,但在慢性羊膜腔内感染后,羊水和解脲脲原体绒毛膜羊膜炎之间检测到显著差异。从绒毛膜羊膜炎(而非羊水)分离出的解脲脲原体23S rRNA基因的V结构域中观察到许多多态性,产生了类似镶嵌的序列。绒毛膜羊膜炎分离株还携带大环内酯类耐药基因erm(B)和msr(D),并与罗红霉素最低抑菌浓度的变化有关。值得注意的是,这种变异性独立于解脲脲原体暴露于红霉素的情况发生,这表明低水平的红霉素暴露不会在子宫内诱导解脲脲原体大环内酯类耐药。相反,羊水和解脲脲原体绒毛膜羊膜炎之间观察到的显著差异表明,不同的解剖部位可能会在非克隆临床菌株中选择解脲脲原体亚型。这可能对宫内解脲脲原体感染的治疗有影响。

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