Please use this identifier to cite or link to this item:http://hdl.handle.net/20.500.12105/5392
Title
Identification and Characterization of Anaplasma phagocytophilum
Proteins Involved in Infection of the Tick Vector, Ixodes scapularis
Author(s)
Villar, Margarita | Ayllon, Nieves | Kocan, Katherine M. | Bonzon-Kulichenko, Elena CNIC | Alberdi, Pilar | Blouin, Edmour F. | Weisheit, Sabine | Mateos-Hernandez, Lourdes | Cabezas-Cruz, Alejandro | Bell-Sakyi, Lesley | Vancova, Marie | Bily, Tomas | Meyer, Damien F. | Sterba, Jan | Contreras, Marinela | Rudenko, Nataliia | Grubhoffer, Libor | Vazquez, Jesus CNIC | de la Fuente, Jose
Date issued
2015
Citation
PLoS One. 2015; 10(9):e0137237
Language
Inglés
Abstract
Anaplasma phagocytophilum is an emerging zoonotic pathogen transmitted
by Ixodes scapularis that causes human granulocytic anaplasmosis. Here,
a high throughput quantitative proteomics approach was used to
characterize A. phagocytophilum proteome during rickettsial
multiplication and identify proteins involved in infection of the tick
vector, I. scapularis. The first step in this research was focused on
tick cells infected with A. phagocytophilum and sampled at two time
points containing 10-15\% and 65-71\% infected cells, respectively to
identify key bacterial proteins over-represented in high percentage
infected cells. The second step was focused on adult female tick guts
and salivary glands infected with A. phagocytophilum to compare in vitro
results with those occurring during bacterial infection in vivo. The
results showed differences in the proteome of A. phagocytophilum in
infected ticks with higher impact on protein synthesis and processing
than on bacterial replication in tick salivary glands. These results
correlated well with the developmental cycle of A. phagocytophilum, in
which cells convert from an intracellular reticulated, replicative form
to the nondividing infectious dense-core form. The analysis of A.
phagocytophilum differentially represented proteins identified stress
response (GroEL, HSP70) and surface (MSP4) proteins that were
over-represented in high percentage infected tick cells and salivary
glands when compared to low percentage infected cells and guts,
respectively. The results demonstrated that MSP4, GroEL and HSP70
interact and bind to tick cells, thus playing a role in rickettsia-tick
interactions. The most important finding of these studies is the
increase in the level of certain bacterial stress response and surface
proteins in A. phagocytophilum-infected tick cells and salivary glands
with functional implication in tick-pathogen interactions. These results
gave a new dimension to the role of these stress response and surface
proteins during A. phagocytophilum infection in ticks. Characterization
of Anaplasma proteome contributes information on host-pathogen
interactions and provides targets for development of novel control
strategies for pathogen infection and transmission.
Subject
IV SECRETION SYSTEM | OUTER-MEMBRANE VESICLES | GENE-EXPRESSION | SURFACE-PROTEINS | DIFFERENTIAL EXPRESSION | CATTLE PATHOGEN | MARGINALE | CELLS | ADHESION | STRESS
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