Black sea cucumber (Holothuria atraJaeger, 1833) rescuesPseudomonas aeruginosa-infectedCaenorhabditis elegans viareduction of pathogen virulence factors and enhancement of host immunity
Author(s) -
Wan-Ting Lee,
Boon-Khai Tan,
Su-Anne Eng,
CheeYuen Gan,
KitLam Chan,
Yee Kwang Sim,
Shaida Fariza Sulaiman,
Alexander Chong ShuChien
Publication year - 2019
Publication title -
food and function
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.145
H-Index - 76
eISSN - 2042-650X
pISSN - 2042-6496
DOI - 10.1039/c9fo01357a
Subject(s) - virulence , pseudomonas aeruginosa , caenorhabditis elegans , biology , host (biology) , microbiology and biotechnology , pathogen , immunity , sea cucumber , immune system , virology , gene , bacteria , ecology , genetics
A strategy to circumvent the problem of multidrug resistant pathogens is the discovery of anti-infectives targeting bacterial virulence or host immunity. Black sea cucumber (Holothuria atra) is a tropical sea cucumber species traditionally consumed as a remedy for many ailments. There is a paucity of knowledge on the anti-infective capacity of H. atra and the underlying mechanisms involved. The objective of this study is to utilize the Caenorhabditis elegans-P. aeruginosa infection model to elucidate the anti-infective properties of H. atra. A bioactive H. atra extract and subsequently its fraction were shown to have the capability of promoting the survival of C. elegans during a customarily lethal P. aeruginosa infection. The same entities also attenuate the production of elastase, protease, pyocyanin and biofilm in P. aeruginosa. The treatment of infected transgenic lys-7::GFP worms with this H. atra fraction restores the repressed expression of the defense enzyme lys-7, indicating an improved host immunity. QTOF-LCMS analysis revealed the presence of aspidospermatidine, an indole alkaloid, and inosine in this fraction. Collectively, our findings show that H. atra possesses anti-infective properties against P. aeruginosa infection, by inhibiting pathogen virulence and, eventually, reinstating host lys-7 expression.
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