Identification and characterization of two highly homologous lysozymes from red swamp crayfish, Procambarus clarkii

IF 2.2 Q2 FISHERIES
Yin Cheng-Ming , Li Ning-Qiu , Ren Li-Chao , Wang Zhe , Chai Lian-Qin , Lan Jiang-Feng
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引用次数: 1

Abstract

Lysozyme is an important immune effector in innate immunity against pathogen infection. But the study on the active region of lysozyme is limited. In this study, two highly homologous lysozymes were identified from crayfish (designated as PcLysi4 and PcLysi5). The molecular structures of PcLysi4 and PcLysi5 were predicted by SWISS-MODEL with the structure of lysozyme (PDB accession No. 4PJ2.2.B) as model. The results suggested that the structure of PcLysi4 and PcLysi5 were highly similar, but there were more α-helices at positions (127–139) and longer β-sheet at positions (49–57) in the structure of PcLysi5 than in that of PcLysi4. The antibacterial and antiviral functions of the two lysozymes were investigated. PcLysi4 and PcLysi5 could promote the bacterial clearance ability of crayfish, and increase the survival rate of Vibrio-infected crayfish. Further study showed that PcLysi5 inhibited WSSV replication, and enhanced the survival rate of WSSV-infected crayfish. There was no evidence that PcLysi4 has an influence on WSSV replication. Furthermore, PcLysi5 was detected to interact with envelope protein VP24 of WSSV. Our results would provide a new reference for the study on active region of lysozyme.

克氏原螯虾(proambarus clarkii)两种高度同源的溶菌酶的鉴定与表征
溶菌酶是先天免疫中抗病原体感染的重要免疫效应器。但对溶菌酶活性区域的研究还很有限。本研究从小龙虾中鉴定出两种高度同源的溶菌酶(命名为PcLysi4和PcLysi5)。以溶菌酶结构(PDB登录号4PJ2.2.B)为模型,采用SWISS-MODEL对PcLysi4和PcLysi5的分子结构进行预测。结果表明,PcLysi4和PcLysi5的结构高度相似,但PcLysi5的结构中(127 ~ 139)处α-螺旋较多,(49 ~ 57)处β-薄片较长。研究了两种溶菌酶的抗菌和抗病毒功能。PcLysi4和PcLysi5能提高小龙虾对细菌的清除能力,提高弧菌感染小龙虾的存活率。进一步研究表明,PcLysi5抑制了WSSV的复制,提高了感染WSSV的小龙虾的存活率。没有证据表明PcLysi4对WSSV复制有影响。此外,PcLysi5还与WSSV的包膜蛋白VP24相互作用。本研究结果将为溶菌酶活性区域的研究提供新的参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.60
自引率
0.00%
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12 weeks
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