首页> 外文期刊>Fish & Shellfish Immunology >Identification of a group D anti-lipopolysaccharide factor (ALF) from kuruma prawn (Marsupenaeus japonicus) with antibacterial activity against Vibrio parahaemolyticus
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Identification of a group D anti-lipopolysaccharide factor (ALF) from kuruma prawn (Marsupenaeus japonicus) with antibacterial activity against Vibrio parahaemolyticus

机译:鉴定Kuruma虾(Marsupenaeus japonicus)的D组抗脂多糖因子(ALF),抗菌活性对抗vibrio parahaemolyticus

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Anti-lipopolysaccharide factor (ALF), which belongs to the antimicrobial peptide (AMP) family, has become a relatively new weapon to combat severe infections and has been demonstrated to be active against bacteria, fungi and some viruses. In the present study, a new ALF of group D (MjALF-D; GenBank accession No. MN416688) from Marsupenaeus japonicas was detected. MjALF-D encodes a polypeptide with 124 aa, and the peptide contains a 26-residue signal peptide and a lipopolysaccharide-binding domain (LBD). The structure of MjALF-D was found to consist of three alpha-helices, four beta-sheets and random coils. qRT-PCR analysis revealed that MjALF-D expression was primarily observed in the stomach and was universally upregulated in both the gill and stomach after challenge by lipopolysaccharide (LPS) and Vibrio parahaemolyticus. Moreover, rMjALF-D can inhibit the growth of V. parahaemolyticus. rMjALF-D could destroy the bacterial membrane and lead to cytoplasmic leakage investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), which may be the mechanism by which rMjALF-D inhibits V. parahaemolyticus. Additionally, rMjALF-D showed distinct binding or antibacterial ability after direct incubation with V. parahaemolyticus or bacterial genomic DNA and a certain effect on the protein expression of it. Together, these results indicated that rMjALF-D possessed the antibacterial activity against V. parahaemolyticus and the potential involvement in the innate immune response of M. japonicas.
机译:属于抗微生物肽(AMP)家族的抗脂多糖因子(ALF)已成为对抗严重感染的相对较新的武器,并且已被证明是针对细菌,真菌和一些病毒的活性。在本研究中,检测来自Marsupenaeus japonicas的D组(Mjalf-d; Genbank登录No.MN416688)的新ALF。 MJALF-D用124AA编码多肽,肽含有26-残基信号肽和脂多糖结合结构域(LBD)。发现MJALF-D的结构由三个α-螺旋,四个β-薄片和随机线圈组成。 QRT-PCR分析显示,MJALF-D在胃中观察到MJALF-D表达,并在脂多糖(LPS)和血管乙酰溶血粒度攻击后在鳃和胃中普遍上调。此外,RMJALF-D可以抑制V.Varahaemolyticus的生长。 RMJALF-D可以破坏细菌膜,并通过扫描电子显微镜(SEM)和透射电子显微镜(TEM)来研究细胞质泄漏,这可能是RMJALF-D抑制V. parahaemolyticus的机制。另外,rmjaLF-D在直接孵育与V.乙酰氨醇或细菌基因组DNA直接孵育后显示出明显的结合或抗菌能力,以及对其蛋白质表达的一定作用。这些结果表明,RMJALF-D具有针对V.Varahaemolyticus的抗菌活性和患有M. japonicas先天免疫应答的潜在参与。

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