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荚膜转换作为在实验性中耳炎模型中增强肺炎球菌毒力的一种策略。

Capsular switching as a strategy to increase pneumococcal virulence in experimental otitis media model.

作者信息

Sabharwal Vishakha, Stevenson Abbie, Figueira Marisol, Orthopoulos George, Trzciński Krzysztof, Pelton Stephen I

机构信息

Section of Pediatric Infectious Diseases, Boston Medical Center, Boston, MA 02118, USA.

Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA.

出版信息

Microbes Infect. 2014 Apr;16(4):292-9. doi: 10.1016/j.micinf.2013.12.002. Epub 2013 Dec 20.

Abstract

We hypothesized that capsular switch event, in which pneumococcus acquires a new capsule operon by horizontal gene transfer, may result in emergence of strains with increased virulence in acute otitis media. Using serotype 6A strain from a patient with invasive pneumococcal disease and clonally distant serotype 6C strain isolated from asymptomatic carrier we created 6A:6C (6A background with 6C capsule) capsular transformants and applied whole genome macro-restriction analysis to assess conservation of the 6A chassis. Next, we assessed complement (C3) and antibodies deposition on surface of pneumococcal cells and tested capsule recipient, capsule donor and two 6A:6C transformants for virulence in chinchilla experimental otitis media model. Both 6A:6C(1 or 2) transformants bound less C3 compared to 6C capsule-donor strain but more compared to serotype 6A capsule-recipient strain. Pneumococci were present in significantly higher proportion of ears among animals challenged with either of two 6A:6C(1 or 2) transformants compared to chinchillas infected with 6C capsule-donor strain [p < 0.001] whereas a significantly decreased proportion of ears were infected with 6A:6C(1 or 2) transformants as compared to 6A capsule-recipient strain. Our observations though limited to two serotypes demonstrate that capsular switch events can result in Streptococcus pneumoniae strains of enhanced virulence for respiratory tract infection.

摘要

我们推测,肺炎球菌通过水平基因转移获得新的荚膜操纵子的荚膜转换事件,可能导致急性中耳炎中出现毒力增强的菌株。我们使用来自侵袭性肺炎球菌病患者的6A血清型菌株和从无症状携带者分离的克隆关系较远的6C血清型菌株,创建了6A:6C(具有6C荚膜的6A背景)荚膜转化体,并应用全基因组宏观限制性分析来评估6A底盘的保守性。接下来,我们评估了补体(C3)和抗体在肺炎球菌细胞表面的沉积,并在龙猫实验性中耳炎模型中测试了荚膜受体、荚膜供体和两种6A:6C转化体的毒力。与6C荚膜供体菌株相比,两种6A:6C(1或2)转化体结合的C3较少,但与6A血清型荚膜受体菌株相比则较多。与感染6C荚膜供体菌株的龙猫相比,用两种6A:6C(1或2)转化体之一攻击的动物中耳中肺炎球菌的比例显著更高[p < 0.001],而与6A荚膜受体菌株相比,感染6A:6C(1或2)转化体的耳朵比例显著降低。我们的观察结果虽然仅限于两种血清型,但表明荚膜转换事件可导致呼吸道感染中毒力增强的肺炎链球菌菌株。

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