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在仓鼠中减毒的一种排除特定病原体的类鼻疽伯克霍尔德菌荚膜突变体

Attenuation of a select agent-excluded Burkholderia pseudomallei capsule mutant in hamsters.

作者信息

Gutierrez Maria G, Warawa Jonathan M

机构信息

Department of Microbiology and Immunology, University of Louisville, Louisville, KY 40202, United States.

Department of Microbiology and Immunology, University of Louisville, Louisville, KY 40202, United States; Center for Predictive Medicine, University of Louisville, Louisville, KY 40202, United States.

出版信息

Acta Trop. 2016 May;157:68-72. doi: 10.1016/j.actatropica.2015.12.006. Epub 2016 Feb 1.

Abstract

Burkholderia pseudomallei is a Tier 1 select agent and potential bioweapon. Given it is potential to cause a lethal respiratory disease, research with fully virulent B. pseudomallei is conducted in Biosafety Level 3 (BSL-3) laboratory spaces. The logistical, financial, and administrative burden of Tier 1 select agent BSL-3 research has created an interest in mitigating such burdens through the use of either attenuated B. pseudomallei strains at BSL-2, or research with surrogate species, such as Burkholderia thailandensis. Previously, attenuated B. pseudomallei auxotroph mutants (asd and purM) have been approved for exclusion from select agent requirements, allowing for in vitro studies to be conducted at BSL-2. Acapsular B. pseudomallei mutants are known to be strongly attenuated in a variety of animal models, and yet acapsular B. pseudomallei mutants do not require nutritional supplementation, and can be studied within cultured macrophages, performing phenotypically similarly to parent strains. We demonstrate that the loss of a 30.8 kb region of the wcb capsule operon allows for a dramatic >4.46 log attenuation in a hamster intraperitoneal infection model, and report that this strain, JW270, has met criteria for exclusion from select agent requirements.

摘要

伯克霍尔德菌是一种一级选择生物制剂和潜在的生物武器。鉴于其有可能引发致命的呼吸道疾病,对完全有毒力的伯克霍尔德菌的研究在生物安全3级(BSL-3)实验室进行。一级选择生物制剂BSL-3研究的后勤、财务和行政负担引发了人们的兴趣,即通过在BSL-2使用减毒伯克霍尔德菌菌株,或使用替代物种(如泰国伯克霍尔德菌)进行研究来减轻此类负担。此前,减毒伯克霍尔德菌营养缺陷型突变体(asd和purM)已被批准无需遵循选择生物制剂的要求,从而可在BSL-2进行体外研究。已知无荚膜伯克霍尔德菌突变体在多种动物模型中强烈减毒,然而无荚膜伯克霍尔德菌突变体无需营养补充,可在培养的巨噬细胞内进行研究,其表型与亲本菌株相似。我们证明,wcb荚膜操纵子30.8 kb区域的缺失在仓鼠腹腔感染模型中可导致超过4.46对数级的显著减毒,并报告该菌株JW270已符合无需遵循选择生物制剂要求的标准。

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