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Journal of Microbiology: Current Research | Volume 2

November 01-02, 2018 | London, UK

7

th

European

Clinical Microbiology Congress

4

th

International Conference on

Ophthalmology and Eye Disorder

Joint Event

&

Management of

Helicobacter pylori

gastric infection via surface-grafted antimicrobial peptides

Paula Parreira

1,2

, Claudia Monteiro

1,2

, Vanessa Graça

2

, Joana Gomes

1,3

, Sílvia Maia

4

, Paula Gomes

4

, Inês C Gonçalves

1,2

and

M Cristina L

Martins

1,2,5*

1

Instituto de Investigação e Inovação em Saúde (i3S), Portugal

2

Instituto de Engenharia Biomédica, Portugal

3

Instituto de Patologia e Imunologia Molecular, Portugal

4

Universidade do Porto, Portugal

5

Instituto de Ciências Biomédicas Abel Salazar, Portugal

H

elicobacter pylori

chronic infection is associated, among

other severe gastric disorders, with intestinal-type gastric

carcinogenesis, being the fifth most common cancer and the

third leading cause of cancer-related death worldwide. Classical

H. pylori

eradication treatment, combining two antibiotics and

a proton pump inhibitor, reduces the risk for gastric carcinoma

development, but treatment of

H. pylori

infection is challenged

by a dramatic fall in eradication rates all over the world.

Currently, this bacterium is listed among the 16 antibiotic-

resistant bacteria that pose greatest threat to human health

according to the World Health Organization. Antimicrobial

peptides (AMPs) present an alternative to conventional

antibiotic therapies, being their most striking feature the low

tendency to induce bacterial resistance, since AMPs selectively

damage the bacterial membranes through mechanisms that

bacteria find difficult to evade. In an

in vivo

scenario, “unbound

AMPs” can undergo proteolysis and peptide aggregation,

leading to efficiency decrease. AMP grafting onto nanoparticles

has been reported as a good strategy to protect peptides from

aggregation and enzymatic degradation

in vivo

, therefore

increasing long-term stability and avoiding cytotoxicity

associated with application of high AMP concentrations. In

this study we demonstrated that the AMP MSI-78A could be

surface-grafted without compromising its activity. Moreover,

MSI-78A-decorated surfaces were highly effective against

H.

pylori

, killing bacteria by contact in a short time span, since

after 2h only 2% of

H. pylori

remained viable in suspension.

These results encourage the utilization of grafted MSI-78A on

biocompatible nanoparticles as an alternative to the currently

available therapy against

H. pylori

, opening new routes for

gastric infection management.

Speaker Biography

Paula Parreira graduated in Microbiology from the Universidade Católica Portuguesa

(Portugal) in 2007. In the same year, joined the team of Prof. M Cristina Martins at the

Institute of Biomedical Engineering of University of Porto (INEB) and from 2007 to 2013,

conducted her PhD studies under the guidance of Prof. M Cristina Martins and Prof.

Deborah Leckband (University of Illinois, at Urbana-Champaign, USA). After finishing

her PhD, Paula Parreira’s post doctoral research has continued to focus on development

of non-antibiotic strategies against microbiological human pathogens, namely against

the gastric pathogen

Helicobacter pylori

, with emphasis on natural molecules coupled

with bioengineered approaches. Currently, Paula Parreira is a research assistant in the

Bioengineered Surfaces Group at Instituto de Investigação e Inovação em Saúde (i3S;

Portugal) and has published several papers in first quartile journals, book chapters and

participated in several international conferences.

e:

parreira@i3s.up.pt

Paula Parreira et al., Clinical Microbiology and Eye 2018, Volume 2

DOI: 10.4066/2591-8036-C1-002