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Notes:
conferenceseries
.com
November 28-29, 2016 Valencia, Spain
4
th
World Congress on
Infection Prevention and Control
Volume 4, Issue 8 (Suppl)
J Infect Dis Ther 2016
ISSN: 2332-0877, JIDT an open access journal
Infection Control 2016
November 28-29, 2016
Lactoferrin is a natural killer of
Candida
spp.
Jack Ho Wong
and
Tzi Bun N G
The Chinese University of Hong Kong, Hong Kong
L
actoferrin is an iron-binding protein in milk. It plays an important role in the host defense system as it prevents microbes from
growing and forming biofilms. In addition to antimicrobial activity, lactoferrin exhibits some anticancer activities. Lactoferricin
(Lfcin) and lactoferrampin (Lfampin), which are peptides derived from lactoferrin, demonstrated antimicrobial activity with
promising prospects and are currently one of the research focuses. We investigated the antifungal effect of these two peptides. We
found that fungal cells exposed to Lfcin manifested morphological alterations, changes in plasma membrane permeability and
mitochondrial membrane potential and ROS accumulation in cells. Lfcin also suppressed superoxide dismutase 3 (SOD3) expression
in the fungal cells. Lfampin exerted its antifungal effect mainly through induction of necrosis. It also induced changes in plasma
membrane permeability and mitochondrial membrane potential. We also tested the effects of the following combinations (1) Lfcin
and Lfampin (2) The Lfcin and Fluconazole and (3) Lfampin and Fluconazole against Candida spp.
Biography
Jack Ho Wong has completed his PhD at the Chinese University of Hong Kong and currently is a Research Associate at the School of Biomedical Sciences. He is
working on bioactive peptides emphasized on antimicrobial and anticancer effect. He has published more than 100 papers in reputed journals and has been serving
as an Editorial Board Member in the journals
Toxins
,
Frontiers in Microbiology
and
Frontiers in Pharmacology
and he is a manuscript Reviewer for several journals.
jack1993@yahoo.comJack Ho Wong et al., J Infect Dis Ther 2016, 4:8 (Suppl)
http://dx.doi.org/10.4172/2332-0877.C1.020