Boddey Justin A, Flegg Cameron P, Day Chris J, Beacham Ifor R, Peak Ian R
Institute for Glycomics, Griffith University, Gold Coast Campus, Gold Coast Mail Centre, Queensland 9726, Australia.
Infect Immun. 2006 Sep;74(9):5374-81. doi: 10.1128/IAI.00569-06.
Burkholderia pseudomallei is the causative agent of melioidosis, a potentially fatal disease that is endemic to Northern Australia and Southeast Asia and is acquired from soil or water. Adherence of B. pseudomallei 08 to cultured cells increases dramatically following prior growth at 30 degrees C or less compared to that following prior growth at 37 degrees C. Here, we show that this occurs almost entirely as the result of microcolony formation (bacterium-bacterium interactions) following growth at 27 degrees C but not at 37 degrees C, which considerably enhances bacterial association with eukaryotic cells. Further, we demonstrate that the type IVA pilin-encoding gene, pilA, is essential for microcolony development by B. pseudomallei 08, and thus optimum association with eukaryotic cells, but is not required for direct adherence (bacterium-cell interactions). In contrast, although the B. pseudomallei genome sequence strain, K96243, also contains transcriptionally active pilA, microcolony formation rarely occurs following growth at either 27 degrees C or 37 degrees C and cell association occurs significantly less than with strain 08. Analysis of pilA transcription in 08 identified that pilA is dramatically upregulated under microcolony-forming conditions, viz., growth at low temperature, and association with eukaryotic cells; the pattern of transcription of pilA in K96243 differed from that in 08. Our study also suggests that biofilm formation by B. pseudomallei 08 and K96243 on polyvinylchloride is not mediated by pilA. Adherence and microcolony formation, and pilA transcription, vary between strains, consistent with known genomic variation in B. pseudomallei, and these phenotypes may be relevant to colonization from the environment.
类鼻疽伯克霍尔德菌是类鼻疽病的病原体,这是一种潜在的致命疾病,在澳大利亚北部和东南亚地区流行,可通过土壤或水传播。与在37℃下预培养相比,类鼻疽伯克霍尔德菌08株在30℃或更低温度下预培养后,其对培养细胞的黏附力显著增加。在此,我们表明,这种情况几乎完全是由于在27℃而非37℃下生长后形成微菌落(细菌-细菌相互作用)所致,这大大增强了细菌与真核细胞的结合。此外,我们证明IVA型菌毛编码基因pilA对类鼻疽伯克霍尔德菌08株的微菌落形成至关重要,因此对与真核细胞的最佳结合也至关重要,但对于直接黏附(细菌-细胞相互作用)并非必需。相比之下,尽管类鼻疽伯克霍尔德菌基因组序列菌株K96243也含有转录活性的pilA,但在27℃或37℃下生长后很少形成微菌落,且细胞结合明显少于08株。对08株pilA转录的分析表明,pilA在微菌落形成条件下,即在低温下生长以及与真核细胞结合时显著上调;K96243中pilA的转录模式与08株不同。我们的研究还表明,类鼻疽伯克霍尔德菌08株和K96243在聚氯乙烯上形成生物膜并非由pilA介导。不同菌株之间的黏附、微菌落形成以及pilA转录存在差异,这与类鼻疽伯克霍尔德菌已知的基因组变异一致,这些表型可能与从环境中定植有关。