发布: 2016年12月05日第6卷第23期 DOI: 10.21769/BioProtoc.2037 浏览次数: 10005
评审: Alexander B. WestbyeMigla MiskinyteAnonymous reviewer(s)
Abstract
Cell wall is a complex biopolymer on the surface of all Gram-positive bacteria. During infection, cell wall is recognized by the innate immune receptor Toll-like receptor 2 causing intense inflammation and tissue damage. In animal models, cell wall traffics from the blood stream to many organs in the body, including brain, heart, placenta and fetus. This protocol describes how to prepare purified cell wall from Streptococcus pneumoniae, detect its distribution in animal tissues, and study the tissue response using the placenta and fetal brain as examples.
Keywords: Cell wall (细胞壁)Background
Host response to infection involves recognition of many bacterial components including the cell wall (CW), a complex macromolecule that forms the surface of all Gram-positive bacteria. The CW of Gram-positive bacteria is formed by the covalent network of peptidoglycan and teichoic acid. Streptococcus pneumoniae, a leading cause of pneumonia, sepsis, and meningitis, has served as an important model organism for studying the innate immune response to Gram-positive bacterial infection including CW.
When upon Streptococcus pneumoniae (pneumococcal) infection CW components are released from bacteria during growth or antibiotic-induced death, it circulates in the blood stream and crosses cellular barriers, including the placenta and blood brain barrier. CW components have inflammatory activities equal to or greater than intact bacteria (Tuomanen et al., 1985a and 1985b). The CW can be viewed as the Gram-positive equivalent of endotoxin. The vast amount of CW pieces released during infection greatly stimulates the host inflammatory response by activating the innate immune receptor, Toll like receptor 2 (TLR2) (Yoshimura et al., 1999). Responses differ depending on the organ infected: the postnatal brain undergoes apoptosis, scarring predominates in heart, and the fetal brain escapes damage, showing striking neuroproliferation (Orihuela et al., 2006; Braun et al., 1999; Fillon et al., 2006; Humann et al., 2016).
This protocol describes how to prepare purified CW from Streptococcus pneumoniae (Tuomanen et al., 1985b) and follow its distribution in mice after intravenous injection, focusing on the placenta and fetal brain as examples (Humann et al., 2016). This model yields histopathologic sections of organs for study of the tissue response to CW components. Our model’s focus on pneumococcal CW derives from its well-described role in inflammation and injury in many organs, its extensive known chemistry and its recognition as a classic TLR2 pathogen associated molecular pattern.
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文章信息
版权信息
© 2016 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Mann, B., Loh, L. N., Gao, G. and Tuomanen, E. (2016). Preparation of Purified Gram-positive Bacterial Cell Wall and Detection in Placenta and Fetal Tissues. Bio-protocol 6(23): e2037. DOI: 10.21769/BioProtoc.2037.
分类
微生物学 > 体内实验模型 > 细菌
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