Sechi Leonardo A, Felis Giovanna E, Ahmed Niyaz, Paccagnini Daniela, Usai Donatella, Ortu Silvia, Molicotti Paola, Zanetti Stefania
Dipartimento di Scienze Biomediche, Sezione di Microbiologia Sperimentale e Clinica, Università degli studi di Sassari, Viale S. Pietro 43/B, 07100 Sassari, Italy.
Infect Genet Evol. 2007 Jul;7(4):424-32. doi: 10.1016/j.meegid.2007.01.001. Epub 2007 Jan 12.
Mycobacterium avium subsp. paratuberculosis (MAP) is the etiological agent of Johne's disease (JD), a chronic gastroenteritis of ruminants and other animals, including primates. Many evidences suggested association of MAP to Crohn's disease, a chronic granulomatous gastrointestinal disease of humans with strong similarities with JD. The present study attempts to evaluate global gene regulation in MAP, which has not been addressed previously, despite the availability of MAP genome sequence. For this purpose, we investigated: (i) the presence of sigma factors and their relationship to sigma factors of other mycobacteria (M. avium subsp.avium, M. tuberculosis, M. bovis, M. leprae and M. smegmatis), and (ii) their expression during different growth conditions and in vitro infection of intestinal epithelial Caco2 cells. MAP genome contains 19 putative sigma factor, but only 12 belong to gene families common to other mycobacteria. Gene expression was evaluated with Real-Time PCR during growth in 7H9 medium and mycobactin J, in 7H9 medium plus mycobactin J and lisozyme, and during infection of Caco2 cells: very different expression patterns were observed and, on the whole, only 7 sigma factors were found to be expressed. sigJ was upregulated during the infection of Caco2 cells. Even if only few sigma factors were expressed in the three conditions tested, the overall high numbers of MAP sigma factors suggests a noteworthy flexibility of this pathogen. Thus, this first report on expression of MAP sigma factors opens the way to an extensive characterization of global gene regulation, as a key to understand strategies of survival and mechanisms of infections used by this organism.
副结核分枝杆菌(MAP)是反刍动物及包括灵长类在内的其他动物的慢性肠胃炎——约内氏病(JD)的病原体。许多证据表明MAP与克罗恩病有关,克罗恩病是一种人类慢性肉芽肿性胃肠疾病,与JD有诸多相似之处。尽管已有MAP基因组序列,但此前尚未有人对MAP的全局基因调控进行评估。本研究旨在对此进行评估。为此,我们研究了:(i)σ因子的存在情况及其与其他分枝杆菌(鸟分枝杆菌亚种鸟分枝杆菌、结核分枝杆菌、牛分枝杆菌、麻风分枝杆菌和耻垢分枝杆菌)的σ因子的关系,以及(ii)它们在不同生长条件下和体外感染肠上皮Caco2细胞期间的表达情况。MAP基因组包含19个假定的σ因子,但只有12个属于其他分枝杆菌共有的基因家族。通过实时定量PCR评估了在7H9培养基和结核分枝杆菌素J中、在7H9培养基加结核分枝杆菌素J和溶菌酶中生长期间以及感染Caco2细胞期间的基因表达:观察到非常不同的表达模式,总体而言,仅发现7个σ因子表达。sigJ在感染Caco2细胞期间上调。即使在所测试的三种条件下只有少数σ因子表达,但MAP的σ因子总数较多表明该病原体具有显著的灵活性。因此,这份关于MAP σ因子表达的首次报告为全面表征全局基因调控开辟了道路,而全局基因调控是理解该生物体生存策略和感染机制的关键。