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Development of a Scrub Typhus Diagnostic Platform Incorporating Cell-Surface Display Technology

Scrub typhus (ST), also known as tsutsugamushi disease and caused by rickettsia Orientia tsutsugamushi, is an underestimated fatal epidemic in the Asia-Pacific region, resulting in a million human infections each year. ST is easily misdiagnosed as clinical diagnosis is based on non-specific skin esc...

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Autores principales: Liao, Chih-Chi, Tsai, Chih-Hsuan, Lo, Huei-Ru, Lin, Pey-Ru, Lin, Chang-Chi, Chao, Yu-Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542878/
https://www.ncbi.nlm.nih.gov/pubmed/34707621
http://dx.doi.org/10.3389/fimmu.2021.761136
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author Liao, Chih-Chi
Tsai, Chih-Hsuan
Lo, Huei-Ru
Lin, Pey-Ru
Lin, Chang-Chi
Chao, Yu-Chan
author_facet Liao, Chih-Chi
Tsai, Chih-Hsuan
Lo, Huei-Ru
Lin, Pey-Ru
Lin, Chang-Chi
Chao, Yu-Chan
author_sort Liao, Chih-Chi
collection PubMed
description Scrub typhus (ST), also known as tsutsugamushi disease and caused by rickettsia Orientia tsutsugamushi, is an underestimated fatal epidemic in the Asia-Pacific region, resulting in a million human infections each year. ST is easily misdiagnosed as clinical diagnosis is based on non-specific skin eschar and flu-like symptoms. Thus, the lack of accurate, convenient, and low-cost detection methods for ST poses a global health threat. To address this problem, we adopted baculovirus surface-display technology to express three variants of TSA56, the major membrane antigen of O. tsutsugamushi, as well as the passenger domain of ScaC (ScaC-PD), on insect Sf21 cell surfaces rather than biosafety level 3 bacteria in an enzyme-linked immunosorbent assay (ELISA). Recombinant TSA56 and ScaC-PD were all properly expressed and displayed on Sf21 cells. Our cell-based ELISA comprising the four antigen-displaying cell types interacted with monoclonal antibodies as well as serum samples from ST-positive field-caught rats. This cell-based ELISA presented high accuracy (96.3%), sensitivity (98.6%), and specificity (84.6%) when tested against the ST-positive rat sera. Results of a pilot study using human sera were also highly consistent with the results of immunofluorescence analyses. By adopting this approach, we circumvented complex purification and refolding processes required to generate recombinant O. tsutsugamushi antigens and reduced the need for expensive equipment and extensively trained operators. Thus, our system has the potential to become a widely used serological platform for diagnosing ST.
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spelling pubmed-85428782021-10-26 Development of a Scrub Typhus Diagnostic Platform Incorporating Cell-Surface Display Technology Liao, Chih-Chi Tsai, Chih-Hsuan Lo, Huei-Ru Lin, Pey-Ru Lin, Chang-Chi Chao, Yu-Chan Front Immunol Immunology Scrub typhus (ST), also known as tsutsugamushi disease and caused by rickettsia Orientia tsutsugamushi, is an underestimated fatal epidemic in the Asia-Pacific region, resulting in a million human infections each year. ST is easily misdiagnosed as clinical diagnosis is based on non-specific skin eschar and flu-like symptoms. Thus, the lack of accurate, convenient, and low-cost detection methods for ST poses a global health threat. To address this problem, we adopted baculovirus surface-display technology to express three variants of TSA56, the major membrane antigen of O. tsutsugamushi, as well as the passenger domain of ScaC (ScaC-PD), on insect Sf21 cell surfaces rather than biosafety level 3 bacteria in an enzyme-linked immunosorbent assay (ELISA). Recombinant TSA56 and ScaC-PD were all properly expressed and displayed on Sf21 cells. Our cell-based ELISA comprising the four antigen-displaying cell types interacted with monoclonal antibodies as well as serum samples from ST-positive field-caught rats. This cell-based ELISA presented high accuracy (96.3%), sensitivity (98.6%), and specificity (84.6%) when tested against the ST-positive rat sera. Results of a pilot study using human sera were also highly consistent with the results of immunofluorescence analyses. By adopting this approach, we circumvented complex purification and refolding processes required to generate recombinant O. tsutsugamushi antigens and reduced the need for expensive equipment and extensively trained operators. Thus, our system has the potential to become a widely used serological platform for diagnosing ST. Frontiers Media S.A. 2021-10-11 /pmc/articles/PMC8542878/ /pubmed/34707621 http://dx.doi.org/10.3389/fimmu.2021.761136 Text en Copyright © 2021 Liao, Tsai, Lo, Lin, Lin and Chao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Liao, Chih-Chi
Tsai, Chih-Hsuan
Lo, Huei-Ru
Lin, Pey-Ru
Lin, Chang-Chi
Chao, Yu-Chan
Development of a Scrub Typhus Diagnostic Platform Incorporating Cell-Surface Display Technology
title Development of a Scrub Typhus Diagnostic Platform Incorporating Cell-Surface Display Technology
title_full Development of a Scrub Typhus Diagnostic Platform Incorporating Cell-Surface Display Technology
title_fullStr Development of a Scrub Typhus Diagnostic Platform Incorporating Cell-Surface Display Technology
title_full_unstemmed Development of a Scrub Typhus Diagnostic Platform Incorporating Cell-Surface Display Technology
title_short Development of a Scrub Typhus Diagnostic Platform Incorporating Cell-Surface Display Technology
title_sort development of a scrub typhus diagnostic platform incorporating cell-surface display technology
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8542878/
https://www.ncbi.nlm.nih.gov/pubmed/34707621
http://dx.doi.org/10.3389/fimmu.2021.761136
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