Department of Biochemistry, Michigan State University, East Lansing, MI 48824, USA.
Brief Funct Genomics. 2010 May;9(3):220-37. doi: 10.1093/bfgp/elq009. Epub 2010 Apr 30.
Mycobacterium avium subspecies paratuberculosis (MAP) is a significant concern to the American and European dairy industries and possibly to human health. MAP possesses the rare ability to survive and replicate in infected macrophages, cells that are typically able to destroy pathogens. Little is known about what changes occur in MAP-infected macrophages that prevent phagosome maturation and lead to intracellular survival of the bacteria. In this study, a bovine immunologically specific cDNA microarray was used to study genes whose expression was altered in monocyte-derived macrophages (MDM) when these cells were infected with 10 different strains of MAP bacteria. Although we used MAP strains isolated from four different host species, cluster analysis of each strains influence in infected MDMs showed no species of origin specific MAP alterations in the host transcriptome. However, MAP strain K10 was observed as a clear outlier in the cluster analysis. Additionally, we observed two SuperShedder MAP strains clustering very closely together compared to the other strains in this study. Overall, microarray analysis yielded 78 annotated genes whose expression was altered by MAP infection, regardless of strain. Few of these genes have been previously studied in the context of Johne's disease or other mycobacterium-caused diseases. Large groups of apoptosis genes, transcription factors and cytokines were found to be differentially expressed in infected monocyte-derived macrophages as well as several genes not previously linked to MAP-host interactions. Identifying novel host genes affected by MAP infection of macrophages may lead to a more complete picture of this complex host-pathogen interaction.
牛分枝杆菌亚种副结核分枝杆菌(MAP)是美国和欧洲奶制品行业的重大关注点,可能也会对人类健康造成影响。MAP 拥有在受感染的巨噬细胞中存活和复制的罕见能力,巨噬细胞通常能够破坏病原体。人们对 MAP 感染巨噬细胞中发生的阻止吞噬体成熟并导致细菌在细胞内存活的变化知之甚少。在这项研究中,使用牛免疫特异性 cDNA 微阵列研究了单核细胞衍生的巨噬细胞(MDM)在感染 10 种不同 MAP 细菌株时基因表达的变化。尽管我们使用了从四种不同宿主物种分离的 MAP 菌株,但对受感染的 MDM 中每种菌株影响的聚类分析表明,宿主转录组中没有特定于 MAP 的起源物种改变。然而,MAP 菌株 K10 在聚类分析中被观察为明显的异常值。此外,与本研究中的其他菌株相比,我们观察到两个超级排放者 MAP 菌株聚类非常接近。总体而言,微阵列分析产生了 78 个注释基因,无论菌株如何,其表达均受 MAP 感染的影响。这些基因中很少有在约翰氏病或其他分枝杆菌引起的疾病背景下进行过研究。在受感染的单核细胞衍生的巨噬细胞中发现了大量凋亡基因、转录因子和细胞因子的表达差异,以及几个以前与 MAP-宿主相互作用无关的基因。确定受 MAP 感染的巨噬细胞影响的新宿主基因可能会更全面地了解这种复杂的宿主-病原体相互作用。