LyeTxI-b, a Synthetic Peptide Derived From Lycosa erythrognatha Spider Venom, Shows Potent Antibiotic Activity in Vitro and in Vivo

被引:32
|
作者
Reis, Pablo V. M. [1 ]
Boff, Daiane [1 ]
Verly, Rodrigo M. [2 ]
Melo-Braga, Marcella N. [1 ]
Cortes, Maria E. [3 ]
Santos, Daniel M. [4 ]
Pimenta, Adriano M. de C. [1 ]
Amaral, Flavio A. [1 ]
Resende, Jarbas M. [5 ]
de Lima, Maria E. [1 ]
机构
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Bioquim & Imunol, Belo Horizonte, MG, Brazil
[2] Univ Fed Vales Jequitinhonha & Mucuri, Fac Ciencias Exatas, Dept Quim, Diamantina, Brazil
[3] Univ Fed Minas Gerais, Fac Odontol, Dept Odontol Restauradora, Belo Horizonte, MG, Brazil
[4] Fundacao Ezequiel Dias, Diretoria Pesquisa & Desenvolvimento, Serv Prote & Aracnideos, Belo Horizonte, MG, Brazil
[5] Univ Fed Minas Gerais, Inst Ciencias Exatas, Dept Quim, Belo Horizonte, MG, Brazil
关键词
LyeTxI; Lycosa erythrognatha; LyeTxI-b; antimicrobial peptide; septic arthritis; PROTEIN SECONDARY STRUCTURE; ANTIMICROBIAL PEPTIDES; STAPHYLOCOCCUS-AUREUS; MEMBRANE INTERACTIONS; SEPTIC ARTHRITIS; RESISTANCE; MODEL; SPECTROSCOPY; CATHELICIDIN; MECHANISMS;
D O I
10.3389/fmicb.2018.00667
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The antimicrobial peptide LyeTxI isolated from the venom of the spider Lycosa erythrognatha is a potential model to develop new antibiotics against bacteria and fungi. In this work, we studied a peptide derived from LyeTxI, named LyeTxI-b, and characterized its structural profile and its in vitro and in vivo antimicrobial activities. Compared to LyeTxI, LyeTxI-b has an acetylated N-terminal and a deletion of a His residue, as structural modifications. The secondary structure of LyeTxI-b is a well-defined helical segment, from the second amino acid to the amidated C-terminal, with no clear partition between hydrophobic and hydrophilic faces. Moreover, LyeTxI-b shows a potent antimicrobial activity against Gram-positive and Gram-negative planktonic bacteria, being 10-fold more active than the native peptide against Escherichia coli. LyeTxI-b was also active in an in vivo model of septic arthritis, reducing the number of bacteria load, the migration of immune cells, the level of IL-1 beta cytokine and CXCL1 chemokine, as well as preventing cartilage damage. Our results show that LyeTxI-b is a potential therapeutic model for the development of new antibiotics against Gram-positive and Gram-negative bacteria.
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页数:12
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