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阳离子氨基酸转运蛋白和鼠伤寒沙门氏菌 ArgT 共同调节精氨酸的可用性,以促进细胞内沙门氏菌的生长。

Cationic amino acid transporters and Salmonella Typhimurium ArgT collectively regulate arginine availability towards intracellular Salmonella growth.

机构信息

Center for Infectious Disease Research and Biosafety Laboratories, Department of Microbiology and Cell Biology, Indian Institute of Science, Bangalore, India.

出版信息

PLoS One. 2010 Dec 3;5(12):e15466. doi: 10.1371/journal.pone.0015466.

Abstract

Cationic amino acid transporters (mCAT1 and mCAT2B) regulate the arginine availability in macrophages. How in the infected cell a pathogen can alter the arginine metabolism of the host remains to be understood. We reveal here a novel mechanism by which Salmonella exploit mCAT1 and mCAT2B to acquire host arginine towards its own intracellular growth within antigen presenting cells. We demonstrate that Salmonella infected bone marrow derived macrophages and dendritic cells show enhanced arginine uptake and increased expression of mCAT1 and mCAT2B. We show that the mCAT1 transporter is in close proximity to Salmonella containing vacuole (SCV) specifically by live intracellular Salmonella in order to access the macrophage cytosolic arginine pool. Further, Lysosome associated membrane protein 1, a marker of SCV, also was found to colocalize with mCAT1 in the Salmonella infected cell. The intra vacuolar Salmonella then acquire the host arginine via its own arginine transporter, ArgT for growth. The argT knockout strain was unable to acquire host arginine and was attenuated in growth in both macrophages and in mice model of infection. Together, these data reveal survival strategies by which virulent Salmonella adapt to the harsh conditions prevailing in the infected host cells.

摘要

阳离子氨基酸转运蛋白(mCAT1 和 mCAT2B)调节巨噬细胞中精氨酸的可用性。在感染细胞中,病原体如何改变宿主的精氨酸代谢仍有待了解。我们在这里揭示了一种新的机制,即沙门氏菌利用 mCAT1 和 mCAT2B 从宿主中获取精氨酸,以促进其在抗原呈递细胞内的自身生长。我们证明,沙门氏菌感染的骨髓来源的巨噬细胞和树突状细胞显示出增强的精氨酸摄取和 mCAT1 和 mCAT2B 的表达增加。我们表明,mCAT1 转运蛋白通过活的细胞内沙门氏菌与沙门氏菌包含的空泡(SCV)密切接近,以便进入巨噬细胞质溶胶精氨酸池。此外,溶酶体相关膜蛋白 1,SCV 的标志物,也在感染细胞中与 mCAT1 共定位。然后,腔内的沙门氏菌通过其自身的精氨酸转运蛋白 ArgT 来获取宿主精氨酸以生长。ArgT 敲除株无法获得宿主精氨酸,在巨噬细胞和感染小鼠模型中的生长均受到抑制。总之,这些数据揭示了毒力沙门氏菌适应感染宿主细胞中恶劣条件的生存策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/703f/2997073/c99f5984384a/pone.0015466.g001.jpg

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