4 / 30
Page 60
Notes:
conferenceseries
.com
Volume 3
Diagnostic Pathology: Open Access
ISSN: 2476-2024
Laboratory Medicine 2018
June 25-26, 2018
June 25-26, 2018 | Berlin, Germany
13
th
International Conference on
Laboratory Medicine & Pathology
The Periplasmic Chaperone Network Of Campylobacter Jejuni: Evidence That SalC (Cj1289) and
PpiD (Cj0694) Are Involved In Maintaining Outer Membrane Integrity
Shadi A Zakai
1
, Aidan J Taylor
2
and
David J Kelly
2
1
King Abdulaziz University, Saudi Arabia
2
University of Sheffield, UK
T
he outer membrane (OM) of Gram-negative pathogenic bacteria is a key structure in host-pathogen interactions that
contains a plethora of proteins, performing a range of functions including adhesion, nutrient uptake, and antimicrobial
resistance. The OM of the food-borne pathogen
Campylobacter jejuni
contains crucial proteins that do this function, and must
be specifically localized to this membrane, but the sorting mechanisms involved are only partially understood. In particular,
chaperones are required to ferry OM proteins across the periplasm after they emerge from the Sec translocation system. In this
work, we have constructed a set of isogenic deletion mutants in genes encoding both known and predicted chaperones (cj0596,
cj0694, cj1069, cj1228c, and cj1289) using NCTC 11168H as the parental strain. These mutants were characterized using a
range of assays to determine effects on growth, agglutination, biofilm formation, membrane permeability and hydrophobicity.
We focused on Cj1289 and Cj0694, which our previous work suggested possessed both chaperone and peptidyl-proyl cis/trans
isomerase (PPIase) domains. Mutants in either cj1289 or cj0694 showed growth defects, increased motility, agglutination and
biofilm formation and severe OM permeability defects. 2D-gel comparisons showed a general decrease in OM proteins in these
mutants. We heterologously overproduced and purified Cj0694 and obtained evidence that this protein was an active PPIase,
as it accelerates the refolding rate of reduced and alkylated ribonuclease T1 and that it also possessed holdase-type chaperone
activity. Cj0694 is most similar to the PpiD class of chaperones but is unusual in possessing PPIase activity. Our data show that
Cj1289 (SalC; SurA-like chaperone) and Cj0694 (PpiD) are key proteins involved in OM biogenesis and integrity in
C. jejuni
.
Biography
Shadi A Zakai has completed his PhD from the University of Sheffield, UK. He currently works in the Department of Medical Microbiology and Parasitology,
Faculty of Medicine, King Abdulaziz University, Kingdom of Saudi Arabia. He has published 4 papers in reputed journals and has been serving as an Editorial
Board Member of repute journals. His research interest include: clinical microbiology, molecular biology, bacterial resistance to antimicrobial agents, and infection
prevention and control.
szakai@kau.edu.saShadi A Zakai et al., Diagn Pathol Open 2018, Volume 3
DOI: 10.4172/2476-2024-C1-003