• Je něco špatně v tomto záznamu ?

Ixodes ricinus defensins attack distantly-related pathogens

M. Tonk, A. Cabezas-Cruz, JJ. Valdés, RO. Rego, L. Grubhoffer, A. Estrada-Peña, A. Vilcinskas, M. Kotsyfakis, M. Rahnamaeian,

. 2015 ; 53 (2) : 358-65. [pub] 20150805

Jazyk angličtina Země Spojené státy americké

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc16028317

Antimicrobial peptides are ubiquitous components of eukaryotic innate immunity. Defensins are a well-known family of antimicrobial peptides, widely distributed in ticks, insects, plants and mammals, showing activity against bacteria, viruses, fungi, yeast and protozoan parasites. Ixodes ricinus is the most common tick species in Europe and is a vector of pathogens affecting human and animal health. Recently, six defensins (including two isoforms) were identified in I. ricinus. We investigated the evolution of the antimicrobial activity of I. ricinus defensins. Among the five unique defensins, only DefMT3, DefMT5 and DefMT6 showed in vitro antimicrobial activity. Each defensin was active against rather distantly-related bacteria (P < 0.05), significantly among Gram-negative species (P < 0.0001). These three defensins represent different clades within the family of tick defensins, suggesting that the last common ancestor of tick defensins may have had comparable antimicrobial activity. Differences in electrostatic potential, and amino acid substitutions in the β-hairpin and the loop bridging the α-helix and β-sheet may affect the antimicrobial activity in DefMT2 and DefMT7, which needs to be addressed. Additionally, the antimicrobial activity of the γ-core motif of selected defensins (DefMT3, DefMT6, and DefMT7) was also tested. Interestingly, compared to full length peptides, the γ-core motifs of these defensins were effective against less species of bacteria. However, the antifungal activity of the γ-core was higher than full peptides. Our results broaden the scope of research in the field of antimicrobial peptides highlighting the overlooked ability of arthropod defensins to act against distantly-related microorganisms.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc16028317
003      
CZ-PrNML
005      
20161021113707.0
007      
ta
008      
161005s2015 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1016/j.dci.2015.08.001 $2 doi
024    7_
$a 10.1016/j.dci.2015.08.001 $2 doi
035    __
$a (PubMed)26255244
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Tonk, Miray $u Fraunhofer Institute for Molecular Biology and Applied Ecology, Department of Bioresources, Winchester Strasse, D-35394 Giessen, Germany. Electronic address: miraytonk@gmail.com.
245    10
$a Ixodes ricinus defensins attack distantly-related pathogens / $c M. Tonk, A. Cabezas-Cruz, JJ. Valdés, RO. Rego, L. Grubhoffer, A. Estrada-Peña, A. Vilcinskas, M. Kotsyfakis, M. Rahnamaeian,
520    9_
$a Antimicrobial peptides are ubiquitous components of eukaryotic innate immunity. Defensins are a well-known family of antimicrobial peptides, widely distributed in ticks, insects, plants and mammals, showing activity against bacteria, viruses, fungi, yeast and protozoan parasites. Ixodes ricinus is the most common tick species in Europe and is a vector of pathogens affecting human and animal health. Recently, six defensins (including two isoforms) were identified in I. ricinus. We investigated the evolution of the antimicrobial activity of I. ricinus defensins. Among the five unique defensins, only DefMT3, DefMT5 and DefMT6 showed in vitro antimicrobial activity. Each defensin was active against rather distantly-related bacteria (P < 0.05), significantly among Gram-negative species (P < 0.0001). These three defensins represent different clades within the family of tick defensins, suggesting that the last common ancestor of tick defensins may have had comparable antimicrobial activity. Differences in electrostatic potential, and amino acid substitutions in the β-hairpin and the loop bridging the α-helix and β-sheet may affect the antimicrobial activity in DefMT2 and DefMT7, which needs to be addressed. Additionally, the antimicrobial activity of the γ-core motif of selected defensins (DefMT3, DefMT6, and DefMT7) was also tested. Interestingly, compared to full length peptides, the γ-core motifs of these defensins were effective against less species of bacteria. However, the antifungal activity of the γ-core was higher than full peptides. Our results broaden the scope of research in the field of antimicrobial peptides highlighting the overlooked ability of arthropod defensins to act against distantly-related microorganisms.
650    _2
$a aminokyselinové motivy $7 D020816
650    _2
$a zvířata $7 D000818
650    _2
$a bakteriální infekce $x imunologie $7 D001424
650    _2
$a biologická evoluce $7 D005075
650    _2
$a kultivované buňky $7 D002478
650    _2
$a defensiny $x genetika $x metabolismus $7 D023082
650    _2
$a interakce hostitele a patogenu $7 D054884
650    _2
$a přirozená imunita $7 D007113
650    _2
$a hmyzí proteiny $x genetika $x metabolismus $7 D019476
650    12
$a klíště $7 D018884
650    _2
$a mykózy $x imunologie $7 D009181
650    _2
$a druhová specificita $7 D013045
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Cabezas-Cruz, Alejandro $u Center for Infection and Immunity of Lille (CIIL), INSERM U1019 - CNRS UMR 8204, Université Lille Nord de France, Institut Pasteur de Lille, Lille, France. Electronic address: cabezasalejandrocruz@gmail.com.
700    1_
$a Valdés, James J $u Biology Centre of the Czech Academy of Sciences, Institute of Parasitology, Branišovská 31, 37005 České Budějovice, Czech Republic. Electronic address: valdjj@gmail.com.
700    1_
$a Rego, Ryan O M $u Biology Centre of the Czech Academy of Sciences, Institute of Parasitology, Branišovská 31, 37005 České Budějovice, Czech Republic. Electronic address: ryanrego@paru.cas.cz.
700    1_
$a Grubhoffer, Libor $u Biology Centre of the Czech Academy of Sciences, Institute of Parasitology, Branišovská 31, 37005 České Budějovice, Czech Republic; University of South Bohemia, Faculty of Science, Branišovská 31, 37005 České Budějovice, Czech Republic. Electronic address: liborex@paru.cas.cz.
700    1_
$a Estrada-Peña, Agustín $u Department of Parasitology, Faculty of Veterinary Medicine, University of Zaragoza, Spain. Electronic address: aestrada@unizar.es.
700    1_
$a Vilcinskas, Andreas $u Fraunhofer Institute for Molecular Biology and Applied Ecology, Department of Bioresources, Winchester Strasse, D-35394 Giessen, Germany; Institute for Phytopathology and Applied Zoology, Justus-Liebig-University of Giessen, Heinrich-Buff-Ring 26-32, D-35392 Giessen, Germany. Electronic address: andreas.vilcinskas@agrar.uni-giessen.de.
700    1_
$a Kotsyfakis, Michalis $u Biology Centre of the Czech Academy of Sciences, Institute of Parasitology, Branišovská 31, 37005 České Budějovice, Czech Republic. Electronic address: mich_kotsyfakis@yahoo.com.
700    1_
$a Rahnamaeian, Mohammad $u Fraunhofer Institute for Molecular Biology and Applied Ecology, Department of Bioresources, Winchester Strasse, D-35394 Giessen, Germany; Department of Parasitology, Faculty of Veterinary Medicine, University of Zaragoza, Spain. Electronic address: mohammad.rahnamaeian@agrar.uni-giessen.de.
773    0_
$w MED00001364 $t Developmental and comparative immunology $x 1879-0089 $g Roč. 53, č. 2 (2015), s. 358-65
856    41
$u https://pubmed.ncbi.nlm.nih.gov/26255244 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20161005 $b ABA008
991    __
$a 20161021114115 $b ABA008
999    __
$a ok $b bmc $g 1166631 $s 952947
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 53 $c 2 $d 358-65 $e 20150805 $i 1879-0089 $m Developmental and comparative immunology $n Dev Comp Immunol $x MED00001364
LZP    __
$a Pubmed-20161005

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...