Chemistry and Biology of Pyoverdines, Pseudomonas Primary Siderophores

被引:102
作者
Cezard, C. [1 ]
Farvacques, N. [1 ,2 ]
Sonnet, P. [1 ,2 ]
机构
[1] Univ Picardie Jules Verne, CNRS, FRE 3517, Lab Glycochim Antimicrobiens & Agroressources,UFR, F-80037 Amiens 01, France
[2] CNRS, FR 3085, Inst Chim Picardie, F-75700 Paris, France
关键词
FpvA; iron; membrane transporter; Pseudomonas; pyoverdine; siderophore; OUTER-MEMBRANE RECEPTOR; MEDIATED IRON UPTAKE; VIRULENCE FACTOR PRODUCTION; EPSILON-AMINO LINK; BACTERIAL CONSTITUENTS; FLUORESCENT PSEUDOMONAS; COORDINATION PROPERTIES; STRUCTURE ELUCIDATION; PLANT-GROWTH; FERRIPYOVERDINE RECEPTOR;
D O I
10.2174/0929867321666141011194624
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pyoverdine is the generic name given to a vast family of fluorescent green-yellowish pigments produced by Pseudomonas species. Pseudomonas aeruginosa is an opportunistic pathogen, particularly infecting humans with compromised natural defenses. These infections result in significantly higher morbidity, longer hospitalization, increased mortality rates and excess health care costs. P. aeruginosa is very difficult to eradicate because of an intrinsic coupled with an adaptive resistance to a wide variety of classical antibiotics. When subjected to iron starvation conditions, Pseudomonas bacteria synthesize pyoverdines, their primary siderophores, to acquire iron from the extracellular medium. These molecules are not only powerful iron(III) scavengers but efficient iron(III) transporters as well. Three distinct structural parts constitute pyoverdines, i.e. (i) the fluorescent chromophore, deriving from a dihydroxyquinoline, attached via its carbonyl group to (ii) a type-specific peptide composed of 6 to 14 amino acids and (iii) a small side chain corresponding to a carboxylic acid derivative. Their chemical structure show three bidentate chelating sites including a catechol and two hydroxamates, leading to an octahedral geometry when complexed to iron(III). While the chromophore group is common to all pyoverdines, their peptide moiety differs among strains and species by the number, length, composition and configuration of amino acids. Following chelation with iron(III), the newly formed pyoverdine-Fe complex is recognized by a specific outer membrane transporter, namely FpvA, and reenters the cell where the iron is released from the pyoverdine into the periplasm for further incorporation into bacterial proteins. The remaining apo-pyoverdine is then recycled and secreted back to the extracellular medium by efflux pumps. Besides, the role of pyoverdines in P. aeruginosa is not only limited to scavenge iron from the bacterial environment. Indeed, these siderophores act as signal molecules for the production of acute virulence factors and are involved in biofilm formation as well. The ongoing expanding pathogenicity of P. aeruginosa has become a major public health problem, and finding alternative strategies to classical antibiotics is urgently needed. Pyoverdines along with the iron pathway recently gained interest among academical researchers as potential new approaches to "fight" the bacteria. This review describes the classification of the nearly 60 pyoverdines identified so far, their structural and chemical properties and their (bio) synthesis. The different mechanisms underlying the steps of a pyoverdine's life in Pseudomonas are detailed as well: the affinity by which a pyoverdine chelates iron(III), the description of the interactions inducing the siderophore-receptor recognition, the specific transport of the pyoverdine-Fe(III) complex. As pyoverdine production and severe infections are linked, we will also report on situations where pyoverdines are considered as being P. aeruginosa Achilles heel: the propensity of FpvA to transport exo-pyoverdines, organic synthesis of pyoverdines and analogs, grafting of antibiotics on pyoverdines in a Trojan Horse strategy.
引用
收藏
页码:165 / 186
页数:22
相关论文
共 169 条
[1]   Substrate specificity of the nonribosomal peptide synthetase PvdD from Pseudomonas aeruginosa [J].
Ackerley, DF ;
Caradoc-Davies, TT ;
Lamont, IL .
JOURNAL OF BACTERIOLOGY, 2003, 185 (09) :2848-2855
[2]   Interaction of TonB with the outer membrane receptor FpvA of Pseudomonas aeruginosa [J].
Adams, Hendrik ;
Zeder-Lutz, Gabrielle ;
Schalk, Isabelle ;
Pattus, Franc ;
Celia, Herve .
JOURNAL OF BACTERIOLOGY, 2006, 188 (16) :5752-5761
[3]   Type II topoisomerase mutations in fluoroquinolone-resistant clinical strains of Pseudomonas aeruginosa isolated in 1998 and 1999:: Role of target enzyme in mechanism of fluoroquinolone resistance [J].
Akasaka, T ;
Tanaka, M ;
Yamaguchi, A ;
Sato, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (08) :2263-2268
[4]   BACTERIAL IRON TRANSPORT - COORDINATION PROPERTIES OF PYOVERDIN PAA, A PEPTIDIC SIDEROPHORE OF PSEUDOMONAS-AERUGINOSA [J].
ALBRECHTGARY, AM ;
BLANC, S ;
ROCHEL, N ;
OCAKTAN, AZ ;
ABDALLAH, MA .
INORGANIC CHEMISTRY, 1994, 33 (26) :6391-6402
[5]  
Amann C, 2000, Z NATURFORSCH C, V55, P671
[6]   Bacterial iron homeostasis [J].
Andrews, SC ;
Robinson, AK ;
Rodríguez-Quiñones, F .
FEMS MICROBIOLOGY REVIEWS, 2003, 27 (2-3) :215-237
[7]   EFFECTS OF SIDEROPHORES ON THE GROWTH OF PSEUDOMONAS-AERUGINOSA IN HUMAN-SERUM AND TRANSFERRIN [J].
ANKENBAUER, R ;
SRIYOSACHATI, S ;
COX, CD .
INFECTION AND IMMUNITY, 1985, 49 (01) :132-140
[8]  
[Anonymous], MONATSH CHEM
[9]   Bacterial iron transport:: 1H NMR determination of the three-dimensional structure of the gallium complex of pyoverdin G4R, the peptidic siderophore of Pseudomonas putida G4R [J].
Atkinson, RA ;
El Din, ALMS ;
Kieffer, B ;
Lefèvre, JF ;
Abdallah, MA .
BIOCHEMISTRY, 1998, 37 (45) :15965-15973
[10]   Iron and Pseudomonas aeruginosa biofilm formation [J].
Banin, E ;
Vasil, ML ;
Greenberg, EP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (31) :11076-11081