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Volume 5, Issue 2 (Suppl)

J Infect Dis Ther 2017

ISSN: 2332-0877, JIDT an open access journal

Infection Congress 2017

May 11-12, 2017

May 11-12, 2017 Barcelona, Spain

4

th

International Congress on

Infectious Diseases

Cell-cell communication between

Plasmodium

and host immune via exosomes

Yifat Ofir-Birin

1

, Xavier Sisquella

2

, Matthew A Pimentel

2

, Jocelyn Sietsma Penington

2

, Anthony T Papenfuss

2

, Ziv Porat

1

, Tal Meningher

3

, Dror Avni

3

, Eli

Schwartz

3

, Andrew Bowie

4

and

Neta Regev-Rudzki

1, 2

1

Weizmann Institute of Science, Israel

2

Walter and Eliza Hall Institute of Medical Research, Australia

3

Sheba Cancer Research Center, Israel

4

Trinity Collage Dublin, Ireland

M

alaria, kills up to a million people each year, is caused by the protozoa of the genus

Plasmodium falciparum

(Pf). These vector-

born parasites cycle between mosquitoes and humans and, in both contexts, are faced with an unstable and hostile environment.

To ensure survival and transmission, the malaria parasite must infect and survive in the human host and differentiate into sexual

forms that are competent for transmission to mosquitoes. We found for the first time that Pf-infected red blood cells (iRBCs) directly

exchange cargo between them using nano-vesicles (exosomes). These tiny vesicles are capable of delivering protected genes to target

cells. Cell-cell communication is a critically important mechanism for information exchange that promotes cell survival. How Pf

parasites sense their host environment and coordinate their actions remain one of the greatest mysteries in malaria. Moreover, our

understanding in the mechanism regulate human immune response to malaria infection is poor. Here, we found that malaria-derived

exosomes carry remarkable cargo providing a secure and efficient mode for signal delivery. We developed an exosomes tracking

assay and could measure Pf exosomes uptake by different cell types. Moreover, although early life-stages of Pf-iRBC are considered

immunologically inert, our initial observations show that ring-stage derived exosomes are immunogenic. We show that exosomes

can specifically activate and induce pro-inflammatory responses, resulting in interferon type I response. This is a new area of malaria

research which may shed a light on the ability of malaria parasite to manipulate their host response.

Biography

Yifat Ofir-Birin is pursuing her Post-doctorate Degree at Dr. Neta Regev - Rudzki’s lab. She is leading an area of research which focuses on “Intercellular

communication between malaria parasites and its human host via extracellular vesicles, exosomes”. During 2013-2015, She was a Senior Scientist at Evogene

R&D while leading an innovative research team in order to find new genes which improve crops traits. She completed her PhD thesis under the supervision of

Professor Ehud Razin. Her thesis demonstrates “The structure and function of the Ap4A-LysRS-MITF pathway in mast cells.

yifat.ofir-birin@wizmann.ac.il

Yifat Ofir-Birin et al., J Infect Dis Ther 2017, 5:2 (Suppl)

http://dx.doi.org/10.4172/2332-0877-C1-023