Blanco Federico Carlos, Klepp Laura Inés, Vazquez Cristina Lourdes, Bigi Fabiana
Institute of Agrobiotechnology and Molecular Biology (IABIMO), National Institute of Agricultural Technology (INTA)-National Scientific and Technical Research Council (CONICET), Hurlingham, Buenos Aires, Argentina.
Institute of Biotechnology, Centre for Veterinary and Agronomics Research (CICVyA), INTA, Nicolás Repetto and De los Reseros, Hurlingham, Buenos Aires, Argentina.
Int J Mycobacteriol. 2025 Apr 1;14(2):140-144. doi: 10.4103/ijmy.ijmy_32_25. Epub 2025 Jun 20.
Bovine tuberculosis (bTB) is a disease primarily caused by Mycobacterium bovis. Currently, no commercial vaccines exist for controlling bTB, making the development of effective vaccine candidates and testing models a high priority. Mouse models are widely used in preclinical trials of anti-TB vaccines. Determining the appropriate cultivation time to assess the mycobacterial load in animal organs or biological samples is crucial to establishing a reliable model that can accurately evaluate the effectiveness of a vaccine candidate. The aim of this study was to assess the growth dynamics and the appearance of colony-forming units (CFUs) in lung homogenates from mice infected with M. bovis. We compared the CFU counts from vaccinated and challenged mice with M. bovis using data from a previous experiment.
CFUs obtained from the lungs of vaccinated and M. bovis-challenged mice of a previous experiment were registered at 3 and 4 weeks of culturing in solid media. The statistical analysis was performed with Kruskal-Wallis, followed by a Dunn's multiple comparison test.
On analyzing the CFU dynamics from lung homogenates, we found that mice vaccinated with Bacillus Calmette-Guérin preserved stable CFU counts after 3 weeks of cultivation on a solid medium. In contrast, both the unvaccinated group and the group vaccinated with an attenuated M. bovis triple mutant strain reached their final CFU counts only after 4 weeks of culturing.
These findings underscore the importance of prolonged follow-up to accurately assess CFU counts, which are crucial for determining vaccine efficacy in trials.
牛结核病(bTB)是一种主要由牛分枝杆菌引起的疾病。目前,尚无用于控制牛结核病的商业疫苗,因此开发有效的候选疫苗和测试模型成为当务之急。小鼠模型广泛用于抗结核疫苗的临床前试验。确定评估动物器官或生物样品中分枝杆菌载量的合适培养时间对于建立能够准确评估候选疫苗有效性的可靠模型至关重要。本研究的目的是评估感染牛分枝杆菌的小鼠肺匀浆中菌落形成单位(CFU)的生长动态和出现情况。我们使用先前实验的数据比较了接种疫苗并感染牛分枝杆菌的小鼠的CFU计数。
将先前实验中接种疫苗和感染牛分枝杆菌的小鼠肺中获得的CFU在固体培养基中培养3周和4周时进行记录。采用Kruskal-Wallis检验进行统计分析,随后进行Dunn多重比较检验。
在分析肺匀浆中的CFU动态时,我们发现接种卡介苗的小鼠在固体培养基上培养3周后CFU计数保持稳定。相比之下,未接种疫苗的组和接种减毒牛分枝杆菌三重突变株的组仅在培养4周后才达到最终CFU计数。
这些发现强调了延长随访时间以准确评估CFU计数的重要性,这对于在试验中确定疫苗疗效至关重要。