Melgarejo Cristian, Cobos Alex, Planas Carles, Fondevila Jaume, Martín Maite, Cervera Zoraida, Cantero Guillermo, Moll Xavier, Espada Yvonne, Domingo Mariano, Vidal Enric, Pérez de Val Bernat
Unitat Mixta d'Investigació IRTA-UAB en Sanitat Animal, Centre de Recerca en Sanitat Animal, Campus de la Universitat Autònoma de Barcelona, Bellaterra, Spain.
IRTA, Programa de Sanitat Animal, Centre de Recerca en Sanitat Animal, Campus de la Universitat Autònoma de Barcelona, Bellaterra, Spain.
Front Microbiol. 2023 Aug 11;14:1236834. doi: 10.3389/fmicb.2023.1236834. eCollection 2023.
Goats are natural hosts of tuberculosis (TB) and are a valid animal model to test new vaccines and treatments to control this disease. In this study, a new experimental model of TB in goats based on the intranasal nebulization of was assessed in comparison with the endobronchial route of infection.
Fourteen animals were divided into two groups of seven and challenged through the endobronchial (EB) and intranasal (IN) routes, respectively. Clinical signs, rectal temperature, body weight, and immunological responses from blood samples were followed up throughout the experiment. All goats were euthanized at 9 weeks post-challenge. Gross pathological examination, analysis of lung lesions using computed tomography, and bacterial load quantification in pulmonary lymph nodes (LNs) by qPCR were carried out.
The IN-challenged group showed a slower progression of the infection: delayed clinical signs (body weight gain reduction, peak of temperature, and apparition of other TB signs) and delayed immunological responses (IFN-γ peak response and seroconversion). At the end of the experiment, the IN group also showed significantly lower severity and dissemination of lung lesions, lower mycobacterial DNA load and volume of lesions in pulmonary LN, and higher involvement of the nasopharyngeal cavity and volume of the lesions in the retropharyngeal LN.
The results indicated that the IN challenge with induced pathological features of natural TB in the lungs, respiratory LN, and extrapulmonary organs but extremely exaggerating the nasopharyngeal TB pathological features. On the other hand, the EB route oversized and accelerated the pulmonary TB lesion progression. Our results highlight the need to refine the inoculation routes in the interest of faithfully reproducing the natural TB infection when evaluating new vaccines or treatments against the disease.
山羊是结核病的天然宿主,是测试控制该疾病的新疫苗和治疗方法的有效动物模型。在本研究中,与支气管内感染途径相比,评估了一种基于鼻内雾化的山羊结核病新实验模型。
将14只动物分为两组,每组7只,分别通过支气管内(EB)和鼻内(IN)途径进行攻击。在整个实验过程中跟踪临床症状、直肠温度、体重以及血液样本的免疫反应。所有山羊在攻击后9周实施安乐死。进行大体病理检查、使用计算机断层扫描分析肺部病变以及通过qPCR对肺淋巴结(LN)中的细菌载量进行定量。
鼻内攻击组显示感染进展较慢:临床症状出现延迟(体重增加减少、体温峰值以及其他结核病症状出现)和免疫反应延迟(IFN-γ峰值反应和血清转化)。在实验结束时,鼻内组还显示肺部病变的严重程度和扩散明显较低,肺LN中的分枝杆菌DNA载量和病变体积较低,以及鼻咽腔受累程度较高和咽后LN中的病变体积较大。
结果表明,用[具体物质未给出]进行鼻内攻击可在肺部、呼吸道LN和肺外器官诱发自然结核病的病理特征,但极大地夸大了鼻咽部结核病的病理特征。另一方面,支气管内途径使肺结核病变进展过度且加速。我们的结果强调,为了在评估针对该疾病的新疫苗或治疗方法时忠实地再现自然结核感染,需要优化接种途径。