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Original Articles
An Evaluation of a New Quantitative Point-of Care Diagnostic to Measure Glucose-6-phosphate Dehydrogenase Activity
Young Yil Bahk, Seong Kyu Ahn, Heung Jin Jeon, Byoung-Kuk Na, Sung-Keun Lee, Ho-Joon Shin
Korean J Parasitol 2022;60(4):281-288.
Published online August 24, 2022
DOI: https://doi.org/10.3347/kjp.2022.60.4.281
Malaria continues to be one of the most crucial infectious burdens in endemic areas worldwide, as well as for travelers visiting malaria transmission regions. It has been reported that 8-aminoquinolines are effective against the Plasmodium species, particularly primaquine, for anti-hypnozoite therapy in P. vivax malaria. However, primaquine causes acute hemolytic anemia in individuals with glucose-6-phosphate dehydrogenase (G6PD) deficiency. Therefore, G6PD deficiency testing should precede hypnozoite elimination with 8-aminoquinoline. Several point-of-care devices have been developed to detect G6PD deficiency. The aim of the present study was to evaluate the performance of a novel, quantitative G6PD diagnostics based on a metagenomic blue fluorescent protein (mBFP). We comparatively evaluated the sensitivity and specificity of the G6PD diagnostic modality with standard methods using 120 human whole blood samples. The G6PD deficiency was spectrophotometrically confirmed. The performance of the G6PD quantitative test kit was compared with that of a licensed control medical device, the G6PD strip. The G6PD quantitative test kit had a sensitivity of 95% (95% confidence interval (CI): 89.3-100%) and a specificity of 100% (95% CI: 94.3-100%). This study shows that the novel diagnostic G6PD quantitative test kit could be a cost-effective and time-efficient, and universally mandated screening tool for G6PD deficiency.

Citations

Citations to this article as recorded by  Crossref logo
  • Performance of quantitative point-of-care tests to measure G6PD activity: An individual participant data meta-analysis
    Arkasha Sadhewa, Ari Winasti Satyagraha, Mohammad Shafiul Alam, Wondimagegn Adissu, Anup Anvikar, Germana Bancone, Praveen K. Bharti, Vinod K. Bhutani, Santasabuj Das, Muzamil Mahdi Abdel Hamid, Mohammad Sharif Hossain, Nitika Nitika, Bernard A. Okech, Ly
    PLOS Neglected Tropical Diseases.2025; 19(3): e0012864.     CrossRef
  • Utilization of Glucose-6-Phosphate Dehydrogenase Test and the Prevalence of Enzyme Deficiency in Korea
    Rihwa Choi, Wonseo Park, Gayoung Chun, Sang Gon Lee, Eun Hee Lee
    Journal of Clinical Medicine.2023; 12(9): 3179.     CrossRef
  • 6,110 View
  • 166 Download
  • 2 Web of Science
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Development and Clinical Evaluation of a Rapid Diagnostic Test for Yellow Fever Non-Structural Protein 1
Yeong Hoon Kim, Tae-Yun Kim, Ji-Seon Park, Jin Suk Park, Jihoo Lee, Joungdae Moon, Chom-Kyu Chong, Ivan Neves Junior, Fernando Raphael Ferry, Hye-Jin Ahn, Lokraj Bhatt, Ho-Woo Nam
Korean J Parasitol 2019;57(3):283-290.
Published online June 30, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.3.283
A rapid diagnostic test (RDT) kit was developed to detect non-structural protein 1 (NS1) of yellow fever virus (YFV) using monoclonal antibody. NS1 protein was purified from the cultured YFV and used to immunize mice. Monoclonal antibody to NS1 was selected and conjugated with colloidal gold to produce the YFV NS1 RDT kit. The YFV RDTs were evaluated for sensitivity and specificity using positive and negative samples of monkeys from Brazil and negative human blood samples from Korea. Among monoclonal antibodies, clones 3A11 and 3B7 proved most sensitive, and used for YFV RDT kit. Diagnostic accuracy of YFV RDT was fairly high; Sensitivity was 0.0% and specificity was 100% against Dengue viruses type 2 and 3, Zika, Chikungunya and Mayaro viruses. This YFV RDT kit could be employed as a test of choice for point-of-care diagnosis and large scale surveys of YFV infection under clinical or field conditions in endemic areas and on the globe.

Citations

Citations to this article as recorded by  Crossref logo
  • Synthesis of Truncated DNA Aptamer and Its Application to an Electrochemical Biosensor Consisting of an Aptamer and a MXene Heterolayer for Yellow Fever Virus
    Nayeon Kwon, Siyun Lee, Moonbong Jang, Jin-Ho Lee, Chulhwan Park, Taek Lee
    BioChip Journal.2024; 18(1): 93.     CrossRef
  • Challenges in Direct Detection of Flaviviruses: A Review
    Bruna de Paula Dias, Camila Cavadas Barbosa, Cyntia Silva Ferreira, Samara Mayra Soares Alves dos Santos, Orlando Alfredo Pineda Arrieta, Wellington Carvalho Malta, Maria Laura Maximiano Dias Gomes, Mariela Alves e Silva, Júlia de Matos Fonseca, Lysandro
    Pathogens.2023; 12(5): 643.     CrossRef
  • A Chikungunya Virus Multiepitope Recombinant Protein Expressed from the Binary System Insect Cell/Recombinant Baculovirus Is Useful for Laboratorial Diagnosis of Chikungunya
    Leonardo Assis da Silva, Monique da Rocha Queiroz Lima, Brenda Rabello de Camargo, Dyeferson Kened da Silva Coelho Guimarães, Anabele Azevedo Lima Barbastefano, Raquel Curtinhas de Lima, Paulo Vieira Damasco, Rivaldo Venâncio da Cunha, Luiz José de Souza,
    Microorganisms.2022; 10(7): 1451.     CrossRef
  • 8,444 View
  • 156 Download
  • 4 Web of Science
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Development of a Rapid Diagnostic Test Kit to Detect IgG/IgM Antibody against Zika Virus Using Monoclonal Antibodies to the Envelope and Non-structural Protein 1 of the Virus
Yeong Hoon Kim, Jihoo Lee, Young-Eun Kim, Chom-Kyu Chong, Yanaihara Pinchemel, Francis Reisdo?rfer, Joyce Brito Coelho, Ronaldo Ferreira Dias, Pan Kee Bae, Zuinara Pereira Maia Gusma?o, Hye-Jin Ahn, Ho-Woo Nam
Korean J Parasitol 2018;56(1):61-70.
Published online February 28, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.1.61
We developed a Rapid Diagnostic Test (RDT) kit for detecting IgG/IgM antibodies against Zika virus (ZIKV) using monoclonal antibodies to the envelope (E) and non-structural protein 1 (NS1) of ZIKV. These proteins were produced using baculovirus expression vector with Sf9 cells. Monoclonal antibodies J2G7 to NS1 and J5E1 to E protein were selected and conjugated with colloidal gold to produce the Zika IgG/IgM RDT kit (Zika RDT). Comparisons with ELISA, plaque reduction neutralization test (PRNT), and PCR were done to investigate the analytical sensitivity of Zika RDT, which resulted in 100% identical results. Sensitivity and specificity of Zika RDT in a field test was determined using positive and negative samples from Brazil and Korea. The diagnostic accuracy of Zika RDT was fairly high; sensitivity and specificity for IgG was 99.0 and 99.3%, respectively, while for IgM it was 96.7 and 98.7%, respectively. Cross reaction with dengue virus was evaluated using anti-Dengue Mixed Titer Performance Panel (PVD201), in which the Zika RDT showed cross-reactions with DENV in 16.7% and 5.6% in IgG and IgM, respectively. Cross reactions were not observed with West Nile, yellow fever, and hepatitis C virus infected sera. Zika RDT kit is very simple to use, rapid to assay, and very sensitive, and highly specific. Therefore, it would serve as a choice of method for point-of-care diagnosis and large scale surveys of ZIKV infection under clinical or field conditions worldwide in endemic areas.

Citations

Citations to this article as recorded by  Crossref logo
  • Development of a colloidal gold immunochromatographic strip to detect equine infectious anemia virus
    Jianzhong Wang, Jicheng Qiu, Mengmeng Wang, Xiaojie Wu, Xiaoguang Li, Heng Zhang
    Virology Journal.2025;[Epub]     CrossRef
  • The Expanding Toolkit of Insect Cell Culture: A New Era in Biotechnology
    Surjeet Kumar Arya, Cynthia L. Goodman, Subba Reddy Palli
    Current Opinion in Insect Science.2025; : 101465.     CrossRef
  • Advances in Metallic-Based Localized Surface Plasmon Sensors for Enhanced Tropical Disease Detection: A Comprehensive Review
    Sajid Farooq, Denise Maria Zezell
    Plasmonics.2024; 19(4): 1721.     CrossRef
  • Diagnostic accuracy of DPP Fever Panel II Asia tests for tropical fever diagnosis
    Sandhya Dhawan, Sabine Dittrich, Sonia Arafah, Stefano Ongarello, Aurelian Mace, Siribun Panapruksachat, Latsaniphone Boutthasavong, Aphaphone Adsamouth, Soulignasak Thongpaseuth, Viengmon Davong, Manivanh Vongsouvath, Elizabeth A. Ashley, Matthew T. Robi
    PLOS Neglected Tropical Diseases.2024; 18(4): e0012077.     CrossRef
  • Hyperendemic Dengue and Possible Zika Circulation in the Westernmost Region of the Indonesian Archipelago
    Harapan Harapan, Kritu Panta, Alice Michie, Timo Ernst, Suzi McCarthy, Muhsin Muhsin, Safarianti Safarianti, Tjut Mariam Zanaria, Mudatsir Mudatsir, R. Tedjo Sasmono, Allison Imrie
    Viruses.2022; 14(2): 219.     CrossRef
  • Engineered NS1 for Sensitive, Specific Zika Virus Diagnosis from Patient Serology
    Thai Leong Yap, Shin Yee Hong, Jun Hui Soh, Lekha Ravichandraprabhu, Vanessa W.X. Lim, Hsi-Min Chan, Tommy Z.X. Ong, Ying Ping Chua, Shi En Koh, Huajing Wang, Yee Sin Leo, Jackie Y. Ying, William Sun
    Emerging Infectious Diseases.2021; 27(5): 1427.     CrossRef
  • Development and characterization of mouse monoclonal antibodies targeting to distinct epitopes of Zika virus envelope protein for specific detection of Zika virus
    Chia-Jung Li, Ping-Han Huang, Hui-Wen Chen, Shih-Chung Chang
    Applied Microbiology and Biotechnology.2021; 105(11): 4663.     CrossRef
  • Recent advances in point-of-care biosensors for the diagnosis of neglected tropical diseases
    Patricia Batista Deroco, Dagwin Wachholz Junior, Lauro Tatsuo Kubota
    Sensors and Actuators B: Chemical.2021; 349: 130821.     CrossRef
  • Solutions against emerging infectious and noninfectious human diseases through the application of baculovirus technologies
    Alexandra Marisa Targovnik, Jorge Alejandro Simonin, Gregorio Juan Mc Callum, Ignacio Smith, Franco Uriel Cuccovia Warlet, María Victoria Nugnes, María Victoria Miranda, Mariano Nicolás Belaich
    Applied Microbiology and Biotechnology.2021; 105(21-22): 8195.     CrossRef
  • Strategies for developing sensitive and specific nanoparticle-based lateral flow assays as point-of-care diagnostic device
    Jun Hui Soh, Hsi-Min Chan, Jackie Y. Ying
    Nano Today.2020; 30: 100831.     CrossRef
  • Evolutions and upcoming on Zika virus diagnosis through an outbreak: A systematic review
    Fernando A. Jorge, Mateus V. Thomazella, Deborah de Castro Moreira, Luciana D. G. Lopes, Jorge J. V. Teixeira, Dennis A. Bertolini
    Reviews in Medical Virology.2020;[Epub]     CrossRef
  • Zika virus serological diagnosis: commercial tests and monoclonal antibodies as tools
    Isaura Beatriz Borges Silva, Aldacilene Souza da Silva, Mariana Sequetin Cunha, Aline Diniz Cabral, Kelly Cristina Alves de Oliveira, Elizabeth De Gaspari, Carlos Roberto Prudencio
    Journal of Venomous Animals and Toxins including Tropical Diseases.2020;[Epub]     CrossRef
  • ZIKV-Specific NS1 Epitopes as Serological Markers of Acute Zika Virus Infection
    Yiu-Wing Kam, Juliana Almeida Leite, Siti Naqiah Amrun, Fok-Moon Lum, Wearn-Xin Yee, Farhana Abu Bakar, Kai Er Eng, David C Lye, Yee-Sin Leo, Chia-Yin Chong, Andre Ricardo Ribas Freitas, Guilherme Paier Milanez, Jose Luiz Proença-Modena, Laurent Rénia, Fa
    The Journal of Infectious Diseases.2019; 220(2): 203.     CrossRef
  • Seasonal dengue surge: Providers⬨tm) perceptions about the impact of dengue on patient volume, staffing and use of point of care testing in Indian emergency departments
    Janice Blanchard, Katherine Douglass, Shweta Gidwani, Usha Khatri, Daniel Gaballa, Amelia Pousson, Neeraj Mangla, Jeffrey Smith
    Journal of Infection and Public Health.2019; 12(6): 794.     CrossRef
  • Development and Clinical Evaluation of a Rapid Diagnostic Test for Yellow Fever Non-Structural Protein 1
    Yeong Hoon Kim, Tae-Yun Kim, Ji-Seon Park, Jin Suk Park, Jihoo Lee, Joungdae Moon, Chom-Kyu Chong, Ivan Neves Junior, Fernando Raphael Ferry, Hye-Jin Ahn, Lokraj Bhatt, Ho-Woo Nam
    The Korean Journal of Parasitology.2019; 57(3): 283.     CrossRef
  • Zika Fever: Development of Diagnostics, Prevention and Treatment
    E. I. Kazachinskaya, D. V. Shan’shin, A. V. Ivanova
    Problems of Particularly Dangerous Infections.2019; (2): 6.     CrossRef
  • High correlation between Zika virus NS1 antibodies and neutralizing antibodies in selected serum samples from normal healthy Thais
    Wannapa Sornjai, Suwipa Ramphan, Nitwara Wikan, Prasert Auewarakul, Duncan R. Smith
    Scientific Reports.2019;[Epub]     CrossRef
  • Generation and Characterization of a Polyclonal Antibody Against NS1 Protein for Detection of Zika Virus
    Liding Zhang, Congjie Chen, Zhixin Chen, Shuzhen He, Yuzhu Song, Xueshan Xia, Qinqin Han, Jinyang Zhang
    Jundishapur Journal of Microbiology.2019;[Epub]     CrossRef
  • Chaperones, Membrane Trafficking and Signal Transduction Proteins Regulate Zaire Ebola Virus trVLPs and Interact With trVLP Elements
    Dong-Shan Yu, Tian-Hao Weng, Chen-Yu Hu, Zhi-Gang Wu, Yan-Hua Li, Lin-Fang Cheng, Nan-Ping Wu, Lan-Juan Li, Hang-Ping Yao
    Frontiers in Microbiology.2018;[Epub]     CrossRef
  • Analysis of Zika virus neutralizing antibodies in normal healthy Thais
    Wannapa Sornjai, Janejira Jaratsittisin, Prasert Auewarakul, Nitwara Wikan, Duncan R. Smith
    Scientific Reports.2018;[Epub]     CrossRef
  • 15,165 View
  • 415 Download
  • 20 Web of Science
  • Crossref