Nonribosomal cyclic peptides: specific markers of fungal infections

被引:24
作者
Jegorov, Alexandr
Haiduch, Marian
Sulc, Miroslav
Havlicek, Vladimir
机构
[1] Acad Sci Czech Republ, Inst Microbiol, CZ-14220 Prague 4, Czech Republic
[2] IVAX Pharmaceut, CZ-37005 Ceske Budejovice, Czech Republic
[3] Palacky Univ, Expt Med Lab, Dept Pediat, CZ-77520 Olomouc, Czech Republic
[4] Palacky Univ, Expt Med Lab, Dept Oncol, CZ-77520 Olomouc, Czech Republic
[5] Univ Hosp Olomouc, CZ-77520 Olomouc, Czech Republic
来源
JOURNAL OF MASS SPECTROMETRY | 2006年 / 41卷 / 05期
关键词
peptide; cyclic; depsipeptide; mass spectrometry; fungal marker; infection; diagnosis; diagnostics; activity; nonribosomal; NRPS; beauverolide; roseotoxin; destruxin; cyclosporin; Aspergillus; Pseudallescheria; Candida; Scedosporium;
D O I
10.1002/jms.1042
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Some cyclic peptides and depsipeptides are synthesized in microorganisms by large multienzymes called nonribosomal peptide synthetases. The structures of peptide products originating in this way are complex and diverse and are microorganism-specific. This work proposes the use of fungal cyclic peptides and depsipeptides as extremely specific markers of fungal infections. Since a reliable molecular tool for diagnosing fungal infections at an early stage is still missing, we present mass spectrometry as a new, modern, broadband (with respect to fungal strain) and specific tool for clinical mycologists. More than 40 different fungal species can be rapidly characterized according to specific families of cyclic peptides, and in some cases, a particular fungal strain can be identified on the basis of its cyclopeptide profile. This paper is also aimed at initiating discussion on the biological role of these secondary metabolites, especially of those synthesized by medically important strains. Proven cytotoxic, anti-inflammatory or immunosuppressive activities of some cyclic peptides indicate that these molecules may contribute to the synergistic array of fungal virulence factors and support microbial invasion during fungal infection. In addition to an overview on recent mass spectrometric protocols for cyclic peptide sequencing, the structures of new peptides from Paecilomyces and Pseudallescheria are presented. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:563 / 576
页数:14
相关论文
共 198 条
[1]  
Alexander B D, 2002, Transpl Infect Dis, V4 Suppl 3, P32, DOI 10.1034/j.1399-3062.4.s3.5.x
[2]   Natural product family 18 chitinase inhibitors [J].
Andersen, OA ;
Dixon, MJ ;
Eggleston, IM ;
van Aalten, DMF .
NATURAL PRODUCT REPORTS, 2005, 22 (05) :563-579
[3]   Friulimicins:: Novel lipopeptide antibiotics with peptidoglycan synthesis inhibiting activity from Actinoplanes friuliensis sp nov I.: Taxonomic studies of the producing microorganism and fermentation [J].
Aretz, W ;
Meiwes, J ;
Seibert, G ;
Vobis, G ;
Wink, J .
JOURNAL OF ANTIBIOTICS, 2000, 53 (08) :807-815
[4]  
Atkins Simon D., 2004, Journal of Applied Genetics, V45, P3
[5]  
BARROW CJ, 1994, J ANTIBIOT, V47, P1182
[6]  
Bernard M, 2001, MED MYCOL, V39, P9, DOI 10.1080/mmy.39.1.9.17
[7]  
Bhatnagar D, 2002, CHEM IMMUNOL, V81, P167
[8]   MONOCLONAL-ANTIBODIES TO THE MULTIENZYME ENNIATIN SYNTHETASE - PRODUCTION AND USE IN STRUCTURAL STUDIES [J].
BILLICH, A ;
ZOCHER, R ;
KLEINKAUF, H ;
BRAUN, DG ;
LAVANCHY, D ;
HOCHKEPPEL, HK .
BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1987, 368 (05) :521-529
[9]   CONSTITUTIVE EXPRESSION OF ENNIATIN SYNTHETASE DURING FERMENTATIVE GROWTH OF FUSARIUM-SCIRPI [J].
BILLICH, A ;
ZOCHER, R .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1988, 54 (10) :2504-2509
[10]   The cyclic structure of microcin J25, a 21-residue peptide antibiotic from Escherichia coli [J].
Blond, A ;
Péduzzi, J ;
Goulard, C ;
Chiuchiolo, MJ ;
Barthélémy, M ;
Prigent, Y ;
Salomón, RA ;
Farías, RN ;
Moreno, F ;
Rebuffat, S .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1999, 259 (03) :747-755