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Antimicrobial peptides from the skin secretions of the New World frogs Lithobates capito and Lithobates warszewitschii (Ranidae)
- Source :
- Peptides, Peptides, Elsevier, 2009, 30 (10), pp.1775-1781. ⟨10.1016/j.peptides.2009.07.011⟩
- Publication Year :
- 2009
- Publisher :
- HAL CCSD, 2009.
-
Abstract
- Taxonomic revisions within the anuran family Ranidae have established the genus Lithobates that currently comprises 49 species of frogs from the New World. Peptidomic analysis, using reversed-phase HPLC with on-line detection by electrospray mass spectrometry, has led to the identification of multiple antimicrobial peptides in norepinephrine-stimulated skin secretions of the North American frog Lithobates capito and the Central American frog Lithobates warszewitschii . Structural characterization of the peptides demonstrated that the L. capito secretions contained brevinin-1 (1), esculentin-1 (1), esculentin-2 (1), ranatuerin-2 (3), and temporin (2) peptides. L. warszewitschii secretions contained brevinin-1 (1), esculentin-2 (1), ranatuerin-2 (2), and temporin (1) peptides. Values in parentheses indicate number of peptides in each family. Temporin-CPa from L. capito , with the atypical structure IPPFIKKVLTTVF·NH 2 , also showed atypical growth-inhibitory activity having greater potency against Escherichia coli (MIC = 25 μM) and Candida albicans (MIC = 25 μM) than against Staphylococcus aureus (MIC = 50 μM). Phylogenetic analysis based upon the amino acid sequences of 37 ranatuerin-2 peptides from 17 species belonging to the genus Lithobates provides support for currently accepted taxonomic relationships. L. capito is sister-group to Lithobates sevosus in a clade that also contains Lithobates areolatus , and Lithobates palustris . L. warszewitschii is most closely related to the Central American species Lithobates tarahumarae and Lithobates vaillanti .
- Subjects :
- 0106 biological sciences
Bodily Secretions
Ranidae
Physiology
[SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology
MESH: Amino Acid Sequence
[CHIM.THER]Chemical Sciences/Medicinal Chemistry
01 natural sciences
Biochemistry
Rana areolata
MESH: Bodily Secretions
Endocrinology
Anti-Infective Agents
Salientia
[SDV.BC.IC]Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB]
MESH: Animals
MESH: Phylogeny
Phylogeny
Antibacterial agent
Skin
0303 health sciences
MESH: Microbial Sensitivity Tests
biology
MESH: Ranidae
Ecology
Lithobates
MESH: Antimicrobial Cationic Peptides
MESH: Hemolysis
Lithobates tarahumarae
Antimicrobial peptides
Molecular Sequence Data
MESH: Anti-Infective Agents
MESH: Sequence Alignment
Zoology
Microbial Sensitivity Tests
010603 evolutionary biology
Hemolysis
03 medical and health sciences
Cellular and Molecular Neuroscience
MESH: Skin
Animals
Humans
Amino Acid Sequence
030304 developmental biology
MESH: Humans
MESH: Molecular Sequence Data
biology.organism_classification
Temporin
[SDV.SP.PHARMA]Life Sciences [q-bio]/Pharmaceutical sciences/Pharmacology
Frog Skin
Sequence Alignment
Antimicrobial Cationic Peptides
Subjects
Details
- Language :
- English
- ISSN :
- 01969781
- Database :
- OpenAIRE
- Journal :
- Peptides, Peptides, Elsevier, 2009, 30 (10), pp.1775-1781. ⟨10.1016/j.peptides.2009.07.011⟩
- Accession number :
- edsair.doi.dedup.....df243e4c2da30c19494c125d39cf3fdf