Department of Microbiology, Immunology and Pathology, Rocky Mountain Regional Center of Excellence for Biodefense and Emerging Infectious Diseases Research, Colorado State University, Fort Collins, Colorado 80523-2025, USA.
Infect Immun. 2010 Jul;78(7):3136-43. doi: 10.1128/IAI.01313-09. Epub 2010 Apr 19.
Burkholderia pseudomallei causes the disease melioidosis in humans and is classified as a category B select agent. Research utilizing this pathogen is highly regulated in the United States, and even basic studies must be conducted in biosafety level 3 (BSL-3) facilities. There is currently no attenuated B. pseudomallei strain available that is excluded from select-agent regulations and can be safely handled at BSL-2 facilities. To address this need, we created Bp82 and Bp190, which are DeltapurM derivatives of B. pseudomallei strains 1026b and K96243 that are deficient in adenine and thiamine biosynthesis but replication competent in vitro in rich medium. A series of animal challenge studies was conducted to ensure that these strains were fully attenuated. Whereas the parental strains 1026b and K96243 and the complemented mutants Bp410 and Bp454 were virulent in BALB/c mice following intranasal inoculation, the DeltapurM mutants Bp82 and Bp190 were avirulent even when they were administered at doses 4 logs higher than the doses used for the parental strains. Animals challenged with high doses of the DeltapurM mutants rapidly cleared the bacterium from tissues (lung, liver, and spleen) and remained free of culturable bacteria for the duration of the experiments (up to 60 days postinfection). Moreover, highly susceptible 129/SvEv mice and immune incompetent mice (IFN-gamma-/-, SCID) were resistant to challenges with DeltapurM mutant Bp82. This strain was also avirulent in the Syrian hamster challenge model. We concluded that DeltapurM mutant Bp82 is fully attenuated and safe for use under BSL-2 laboratory conditions and thus is a candidate for exclusion from the select-agent list.
类鼻疽伯克霍尔德菌会导致人类类鼻疽病,被归类为 B 类选择剂。在美国,利用这种病原体进行的研究受到高度监管,即使是基础研究也必须在生物安全级别 3(BSL-3)设施中进行。目前没有可用的减毒类鼻疽伯克霍尔德菌菌株,它不受选择剂法规的限制,可以在 BSL-2 设施中安全处理。为了解决这一需求,我们创建了 Bp82 和 Bp190,它们是类鼻疽伯克霍尔德菌菌株 1026b 和 K96243 的 DeltapurM 衍生物,它们在腺嘌呤和硫胺素生物合成中缺失,但在富含培养基的体外具有复制能力。进行了一系列动物挑战研究,以确保这些菌株完全减毒。虽然亲本菌株 1026b 和 K96243 以及互补突变体 Bp410 和 Bp454 在 BALB/c 小鼠中经鼻腔接种后具有毒力,但 DeltapurM 突变体 Bp82 和 Bp190 即使在给予比亲本菌株高 4 个对数剂量的剂量时也没有毒力。用高剂量 DeltapurM 突变体挑战的动物迅速从组织(肺、肝和脾)中清除细菌,并在实验期间(感染后长达 60 天)保持无可培养细菌。此外,高度易感的 129/SvEv 小鼠和免疫功能不全的小鼠(IFN-γ-/-,SCID)对 DeltapurM 突变体 Bp82 的挑战具有抗性。该菌株在叙利亚仓鼠挑战模型中也没有毒力。我们得出结论,DeltapurM 突变体 Bp82 完全减毒,可在 BSL-2 实验室条件下安全使用,因此是从选择剂清单中排除的候选物。