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6型血清群O抗原的构象与免疫原性研究:O-乙酰化的影响

Conformational and Immunogenicity Studies of the Serogroup 6 O-Antigen: The Effect of O-Acetylation.

作者信息

Richardson Nicole Inge, Ravenscroft Neil, Arato Vanessa, Oldrini Davide, Micoli Francesca, Kuttel Michelle M

机构信息

Department of Chemistry, University of Cape Town, Rondebosch 7701, South Africa.

GSK Vaccines Institute for Global Health (GVGH) S.r.l., via Florentina 1, 53100 Siena, Italy.

出版信息

Vaccines (Basel). 2021 Apr 27;9(5):432. doi: 10.3390/vaccines9050432.

Abstract

The pathogenic bacterium is a leading cause of diarrheal disease and mortality, disproportionately affecting young children in low-income countries. The increasing prevalence of antibiotic resistance in necessitates an effective vaccine, for which the bacterial lipopolysaccharide O-antigen is the primary target. serotype 6 has been proposed as a multivalent vaccine component to ensure broad protection against . We have previously explored the conformations of O-antigens from serogroups Y, 2, 3, and 5 that share a common saccharide backbone (serotype Y). Here we consider serogroup 6, which is of particular interest because of an altered backbone repeat unit with non-stoichiometric O-acetylation, the antigenic and immunogenic importance of which have yet to be established. Our simulations show significant conformational changes in serogroup 6 relative to the serotype Y backbone. We further find that O-acetylation has little effect on conformation and hence may not be essential for the antigenicity of serotype 6. This is corroborated by an in vivo study in mice, using Generalized Modules for Membrane Antigens (GMMA) as O-antigen delivery systems, that shows that O-acetylation does not have an impact on the immune response elicited by the serotype 6 O-antigen.

摘要

这种致病细菌是腹泻疾病和死亡的主要原因,对低收入国家的幼儿影响尤为严重。该细菌中抗生素耐药性的日益普遍使得一种有效的疫苗成为必要,而细菌脂多糖O抗原是主要靶点。6型血清型已被提议作为多价疫苗成分,以确保对该细菌具有广泛的保护作用。我们之前已经探索了来自血清群Y、2、3和5的O抗原的构象,它们共享一个共同的糖骨架(Y血清型)。在这里,我们考虑血清群6,由于其主链重复单元发生改变且存在非化学计量的O-乙酰化,这一点特别令人感兴趣,其抗原性和免疫原性的重要性尚未确定。我们的模拟显示,血清群6相对于Y血清型主链有显著的构象变化。我们进一步发现,O-乙酰化对构象影响很小,因此可能对6型血清型的抗原性并非必不可少。在小鼠体内进行的一项研究证实了这一点,该研究使用膜抗原通用模块(GMMA)作为O抗原递送系统,表明O-乙酰化对6型血清型O抗原引发的免疫反应没有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f981/8144980/583b4f822797/vaccines-09-00432-g001.jpg

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