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生物膜形成在解脲脲原体抗生素敏感性和早产儿支气管肺发育不良发展中的作用。

Role of biofilm formation in Ureaplasma antibiotic susceptibility and development of bronchopulmonary dysplasia in preterm neonates.

机构信息

Department of Pediatrics, University of Maryland, Baltimore, MD 21201, USA.

出版信息

Pediatr Infect Dis J. 2013 Apr;32(4):394-8. doi: 10.1097/INF.0b013e3182791ae0.

Abstract

BACKGROUND

Ureaplasma respiratory tract colonization is a risk factor for bronchopulmonary dysplasia (BPD) in preterm infants, but whether Ureaplasma isolates from colonized infants can form biofilms is unknown. We hypothesized that Ureaplasma isolates vary in capacity to form biofilms that contribute to their antibiotic resistance and ability to evade host immune responses. Study objectives were to (1) determine the ability of Ureaplasma isolates from preterm neonates to form biofilms in vitro; (2) compare the susceptibility of the sessile and planktonic organisms to azithromycin (AZI) and erythromycin; and (3) determine the relationship of biofilm-forming capacity in Ureaplasma isolates and the risk for BPD.

METHODS

Forty-three clinical isolates from preterm neonates and 5 American Tissue Culture Collection strains were characterized for their capacity to form biofilms in vitro, and antibiotic susceptibility was performed on each isolate prebiofilm and postbiofilm formation.

RESULTS

Forty-one (95%) clinical and 4 of 5 (80%) American Tissue Culture Collection isolates formed biofilms. All isolates were more susceptible to AZI (minimum inhibitory concentration, MIC50 2 µg/mL) than erythromycin (MIC50 4 µg/mL), and biofilm formation did not significantly affect antibiotic susceptibility for the 2 tested antibiotics. The MIC50 and minimum biofilm inhibitory concentrations (MBIC50) for Ureaplasma urealyticum clinical isolates for AZI were higher than for MIC50 and MBIC50 for Ureaplasma parvum isolates. There were no differences in MIC or MBICs among isolates from BPD infants and non-BPD infants.

CONCLUSIONS

Capacity to form biofilms is common among Ureaplasma spp. isolates, but biofilm formation did not impact MICs for AZI or erythromycin.

摘要

背景

解脲脲原体呼吸道定植是早产儿支气管肺发育不良(BPD)的危险因素,但定植婴儿的解脲脲原体分离株是否能形成生物膜尚不清楚。我们假设解脲脲原体分离株在形成生物膜的能力上存在差异,这有助于它们对抗生素的耐药性和逃避宿主免疫反应的能力。研究目的是:(1)确定早产儿解脲脲原体分离株在体外形成生物膜的能力;(2)比较浮游生物和固着生物对阿奇霉素(AZI)和红霉素的敏感性;(3)确定解脲脲原体分离株形成生物膜的能力与 BPD 风险的关系。

方法

对 43 株来自早产儿的临床分离株和 5 株美国组织培养物收集株进行体外生物膜形成能力的特征描述,并对每个分离株的生物膜形成前后进行抗生素敏感性测定。

结果

41 株(95%)临床分离株和 5 株(80%)美国组织培养物收集株形成生物膜。所有分离株对 AZI(最小抑菌浓度,MIC50 2μg/ml)的敏感性均高于红霉素(MIC50 4μg/ml),且生物膜形成对 2 种测试抗生素的敏感性无显著影响。Ureaplasma urealyticum 临床分离株的 AZI 的 MIC50 和最小生物膜抑制浓度(MBIC50)高于 Ureaplasma parvum 分离株的 MIC50 和 MBIC50。BPD 婴儿和非 BPD 婴儿分离株的 MIC 和 MBIC 无差异。

结论

解脲脲原体分离株形成生物膜的能力很常见,但生物膜形成并不影响 AZI 或红霉素的 MIC。

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