TY - JOUR
T1 - Discovery of novel Caeridins from the skin secretion of the Australian White’s tree frog, Litoria caerulea
AU - Li, Lei
AU - Wu, Qing
AU - Wang, Xi
AU - Lu, Huimin
AU - Xi, Xinping
AU - Zhou, Mei
AU - Watson, Chris J.
AU - Chen, Tianbao
AU - Wang, Lei
PY - 2018/7/11
Y1 - 2018/7/11
N2 - Abundant biologically active peptides have been discovered from frog skin secretions, a rich natural source of bioactive compounds with great potential in drug discovery. In this study, a Caeridin peptides, namely Caeridin-1, S5-Caeridin-1 and Caeridin-a1 were discovered from the skin secretion of the Australian White’s tree frog, Litoria caerulea for the first time, by means of combining transcriptomic and peptidomic analyses. It also represents the first report on bioactive Caeridins since this family of peptides was initially studied 20 years ago. Chemically-synthetic versions of each natural Caeridin demonstrated promising bioactivities either on rat smooth muscles or against microbial growth. Specifically, Caeridin-1 produced contraction of rat bladder smooth muscle, while S5-Caeridin-1 induced relaxation of rat ileum smooth muscle, both at nanomolar concentrations. Moreover, Caeridin-a1 was shown to potently inhibit the growth of the planktonic Gram-positive bacteria Staphylococcus aureus (S. aureus), methicillin-resistant S. aureus (MRSA) and Enterococcus faecalis (E. faecalis), the Gram-negative bacterium, Escherichia coli (E. coli) and the yeast, Candida albicans (C. albicans). The discovery of these Caeridins may induce further intensive and systematic studies of frog skin peptides to promote the discovery of natural templates as lead compounds for drug discovery and therapeutic application.
AB - Abundant biologically active peptides have been discovered from frog skin secretions, a rich natural source of bioactive compounds with great potential in drug discovery. In this study, a Caeridin peptides, namely Caeridin-1, S5-Caeridin-1 and Caeridin-a1 were discovered from the skin secretion of the Australian White’s tree frog, Litoria caerulea for the first time, by means of combining transcriptomic and peptidomic analyses. It also represents the first report on bioactive Caeridins since this family of peptides was initially studied 20 years ago. Chemically-synthetic versions of each natural Caeridin demonstrated promising bioactivities either on rat smooth muscles or against microbial growth. Specifically, Caeridin-1 produced contraction of rat bladder smooth muscle, while S5-Caeridin-1 induced relaxation of rat ileum smooth muscle, both at nanomolar concentrations. Moreover, Caeridin-a1 was shown to potently inhibit the growth of the planktonic Gram-positive bacteria Staphylococcus aureus (S. aureus), methicillin-resistant S. aureus (MRSA) and Enterococcus faecalis (E. faecalis), the Gram-negative bacterium, Escherichia coli (E. coli) and the yeast, Candida albicans (C. albicans). The discovery of these Caeridins may induce further intensive and systematic studies of frog skin peptides to promote the discovery of natural templates as lead compounds for drug discovery and therapeutic application.
KW - bioactive peptides
KW - peptidomics
KW - antimicrobial assays
KW - biological activities
U2 - 10.1155/2018/8158453
DO - 10.1155/2018/8158453
M3 - Article
C2 - 30116731
VL - 2018
JO - International Journal of Genomics
JF - International Journal of Genomics
SN - 2314-436X
M1 - 8158453
ER -