Javascript must be enabled to continue!
Expression and Refolding of Truncated Recombinant Major Outer Membrane Protein Antigen (r56) of Orientia tsutsugamushi and Its Use in Enzyme-Linked Immunosorbent Assays
View through CrossRef
ABSTRACT
The variable 56-kDa major outer membrane protein of
Orientia tsutsugamushi
is the immunodominant antigen in human scrub typhus infections. The gene encoding this protein from Karp strain was cloned into the expression vector pET11a. The recombinant protein (r56) was expressed as a truncated nonfusion protein (amino acids 80 to 456 of the open reading frame) which formed an inclusion body when expressed in
Escherichia coli
BL21. Refolded r56 was purified and compared to purified whole-cell lysate of the Karp strain of
O. tsutsugamushi
by immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) for reactivity with rabbit sera prepared against eight antigenic prototypes of
O. tsutsugamushi
as well as several other species of
Rickettsiales
and nonrickettsial antigens. Refolded r56 exhibited broad reactivity with the rabbit antisera against the
Orientia
prototypes, and the ELISA reactions with the r56 and Karp whole-cell lysate antigens correlated well (
r
= 0.81,
n
= 22, sensitivity compared to that of standard ELISA of 91%). Refolded r56 did not react with most antisera against other rickettsial species or control antigens (specificity = 92%,
n
= 13) using a positive cutoff value determined with eight uninfected rabbit sera. Refolded r56 was evaluated further by ELISA, using 128 sera obtained from patients with suspected scrub typhus from Korat, Thailand, and 74 serum specimens from healthy Thai soldiers. By using the indirect immunoperoxidase assay as the reference assay, the recombinant antigen exhibited a sensitivity and specificity of 93% or greater for detection of both IgG and IgM in the ELISA at 1:400 serum dilution. These results strongly suggest that purified r56 is a suitable candidate for replacing the density gradient-purified, rickettsia-derived, whole-cell antigen currently used in the commercial dipstick assay available in the United States.
American Society for Microbiology
Title: Expression and Refolding of Truncated Recombinant Major Outer Membrane Protein Antigen (r56) of
Orientia tsutsugamushi
and Its Use in Enzyme-Linked Immunosorbent Assays
Description:
ABSTRACT
The variable 56-kDa major outer membrane protein of
Orientia tsutsugamushi
is the immunodominant antigen in human scrub typhus infections.
The gene encoding this protein from Karp strain was cloned into the expression vector pET11a.
The recombinant protein (r56) was expressed as a truncated nonfusion protein (amino acids 80 to 456 of the open reading frame) which formed an inclusion body when expressed in
Escherichia coli
BL21.
Refolded r56 was purified and compared to purified whole-cell lysate of the Karp strain of
O.
tsutsugamushi
by immunoglobulin G (IgG) enzyme-linked immunosorbent assay (ELISA) for reactivity with rabbit sera prepared against eight antigenic prototypes of
O.
tsutsugamushi
as well as several other species of
Rickettsiales
and nonrickettsial antigens.
Refolded r56 exhibited broad reactivity with the rabbit antisera against the
Orientia
prototypes, and the ELISA reactions with the r56 and Karp whole-cell lysate antigens correlated well (
r
= 0.
81,
n
= 22, sensitivity compared to that of standard ELISA of 91%).
Refolded r56 did not react with most antisera against other rickettsial species or control antigens (specificity = 92%,
n
= 13) using a positive cutoff value determined with eight uninfected rabbit sera.
Refolded r56 was evaluated further by ELISA, using 128 sera obtained from patients with suspected scrub typhus from Korat, Thailand, and 74 serum specimens from healthy Thai soldiers.
By using the indirect immunoperoxidase assay as the reference assay, the recombinant antigen exhibited a sensitivity and specificity of 93% or greater for detection of both IgG and IgM in the ELISA at 1:400 serum dilution.
These results strongly suggest that purified r56 is a suitable candidate for replacing the density gradient-purified, rickettsia-derived, whole-cell antigen currently used in the commercial dipstick assay available in the United States.
Related Results
Comparative evaluation of selected diagnostic assays for the detection of IgG and IgM antibody to Orientia tsutsugamushi in Thailand.
Comparative evaluation of selected diagnostic assays for the detection of IgG and IgM antibody to Orientia tsutsugamushi in Thailand.
We compared the performance of 2 commercially available dipstick assays, 2 enzyme-linked immunosorbent assays (ELISAs), and an indirect immunofluorescent antibody (IFA) assay for t...
Online monitoring of protein refolding in inclusion body processing using intrinsic fluorescence
Online monitoring of protein refolding in inclusion body processing using intrinsic fluorescence
Abstract
Inclusion bodies (IBs) are protein aggregates formed as a result of overexpression of recombinant protein in E. coli. The formation of IBs is a valuable st...
Procedure for Western blot v1
Procedure for Western blot v1
Goal: This document has the objective of standardizing the protocol for Western blot. This technique allows the detection of specific proteins separated on polyacrylamide gel and t...
Acute Ischemic Stroke in Tsutsugamushi: Understanding the Underlying Mechanisms and Risk Factors
Acute Ischemic Stroke in Tsutsugamushi: Understanding the Underlying Mechanisms and Risk Factors
Abstract
Background: Tsutsugamushi (scrub typhus) is an acute infectious febrile disease common in the Asia-Pacific region. Common symptoms of tsutsugamushi include lymphad...
Acute ischemic stroke in Tsutsugamushi: understanding the underlying mechanisms and risk factors
Acute ischemic stroke in Tsutsugamushi: understanding the underlying mechanisms and risk factors
Abstract
Background
Tsutsugamushi (scrub typhus) is an acute infectious febrile disease common in the Asia-Pacific region...
Protein refolding using chemical refolding additives
Protein refolding using chemical refolding additives
AbstractIn laboratories and manufacturing settings, a rapid and inexpensive method for the preparation of a target protein is crucial for promoting resesrach in protein science and...
An Investigation into Hydrophobic Membrane Fouling in Desalination Using Membrane Distillation Technology
An Investigation into Hydrophobic Membrane Fouling in Desalination Using Membrane Distillation Technology
Demand for freshwater supplies is continuously increasing globally to the extent where some parts of the world became highly water stressed. In particular, the Arabian Gulf states ...
Genotype Diversity and Distribution of Orientia tsutsugamushi Causing Scrub Typhus in Thailand
Genotype Diversity and Distribution of Orientia tsutsugamushi Causing Scrub Typhus in Thailand
ABSTRACT
Scrub typhus, caused by antigenically disparate isolates of
Orientia tsutsugamushi
, is a widely distributed mite-borne huma...

