scholarly journals A Simple and Rapid Method of Preparation of Rabbit Antiserum Against Alkyl Hydroperoxide Reductase (Ahpc) of Helicobacter pylori

2008 ◽  
Vol 12 ◽  
pp. e167-e168
Author(s):  
T. Mohammadian ◽  
M. Doosti ◽  
M. Paknejad ◽  
F. Siavoshi ◽  
S. Massarrat ◽  
...  
2005 ◽  
Vol 1753 (2) ◽  
pp. 240-246 ◽  
Author(s):  
Elena Papinutto ◽  
Henry J. Windle ◽  
Laura Cendron ◽  
Roberto Battistutta ◽  
Dermot Kelleher ◽  
...  

Helicobacter ◽  
2001 ◽  
Vol 6 (4) ◽  
pp. 274-282 ◽  
Author(s):  
Jing Yan ◽  
Toshiko Kumagai ◽  
Makoto Ohnishi ◽  
Ichiro Ueno ◽  
Hiroyoshi Ota

Vaccine ◽  
2012 ◽  
Vol 30 (26) ◽  
pp. 3876-3884 ◽  
Author(s):  
Avril A. O’Riordan ◽  
Veronica Athie Morales ◽  
Linda Mulligan ◽  
Nazia Faheem ◽  
Henry J. Windle ◽  
...  

2013 ◽  
Vol 195 (23) ◽  
pp. 5396-5401 ◽  
Author(s):  
S. L. Benoit ◽  
K. Bayyareddy ◽  
M. Mahawar ◽  
J. S. Sharp ◽  
R. J. Maier

2000 ◽  
Vol 68 (2) ◽  
pp. 801-808 ◽  
Author(s):  
Ingrid Olsen ◽  
Liv J. Reitan ◽  
Gudmund Holstad ◽  
Harald G. Wiker

ABSTRACT Antigens characteristic for Mycobacterium aviumsubspecies paratuberculosis were identified by crossed immunoelectrophoresis (CIE) and by absorbing out cross-reactive antigens by using a polyclonal and polyvalent Mycobacterium avium subspecies avium antiserum. Two antigens were present in M. avium subsp. paratuberculosis and not detected in Mycobacterium avium subsp.avium. They were identified as antigens 17 and 20 in a CIE reference system for M. avium subsp.paratuberculosis antigens. Purified antigen 20 was identified as alkyl hydroperoxide reductase C (AhpC) while the N-terminal part of purified antigen 17 showed 80% homology with alkyl hydroperoxide reductase D (AhpD) of Mycobacterium tuberculosis. AhpC had a nonreduced mobility in sodium dodecyl sulfate-polyacrylamide gel electrophoresis corresponding to a molecular mass of 45 kDa and is probably a homodimer linked with disulfide bridges in its native form. AhpD had a mobility corresponding to 19 kDa. Monospecific rabbit antiserum against AhpC and AhpD reacted with 9 strains of M. avium subsp. paratuberculosis but not with 20 other mycobacterial strains except for aMycobacterium gordonae strain, against which a weak cross-reactive band was produced. Goats experimentally infected withM. avium subsp. paratuberculosis had strong gamma interferon (IFN-γ) responses toward both AhpC and AhpD, and they also had antibodies against AhpC. The ability of AhpC and AhpD to induce IFN-γ production shows that these proteins potentially could be used in future vaccines or in diagnostic assays. These results further show that AhpC and AhpD are immunologically important proteins which are constitutively and highly expressed in M. aviumsubsp. paratuberculosis without the bacteria being submitted to oxidative stress and that the specificities of antigens can be a matter of different levels of protein expression in various species as well as distinct structural differences.


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