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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

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    Jianzhong Wang, Jicheng Qiu, Mengmeng Wang, Xiaojie Wu, Xiaoguang Li, Heng Zhang
    Virology Journal.2025;[Epub]     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
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Antibody reaction of human anti-Toxoplasma gondii positive and negative sera with Neospora caninum antigens
Ho-Woo Nam, Seung-Won Kang, Won-Young Choi
Korean J Parasitol 1998;36(4):269-275.
Published online December 20, 1998
DOI: https://doi.org/10.3347/kjp.1998.36.4.269

Anti-Neospora caninum antibody was detected in anti-Toxoplasma gondii positive and negative human sera by ELISA, western blot and immunofluorescence assay (IFA). Twelve cases out of 172 (6.7%) Toxoplasma-positive sera cross-reacted with both T. gondii and N. caninum antigens, and one out of 110 Toxoplasma-negative sera reacted with N. caninum antigen by ELISA. By western blot, all 12 sera reacted with T. gondii antigens with various banding patterns but specifically at 30 kDa (SAG1) and 22 kDa (SAG2) bands. With N. caninum antigen, the number of reactive bands was reduced, however a 43 kDa band reacted in three cases in Toxoplasma-positive sera in addition to one in Toxoplasma-negative control sera. All sera of the Toxoplasma-positive group labeled surface membrane of T. gondii, but reacted differently with N. caninum. Fluorescence was detected in surface membrane, subcellular organelles, or both in N. caninum. And one case in the Toxoplasma-negative group also reacted with N. caninum strongly in subcellular organelles. This suggested that the antibody against N. caninum may be present in human sera although the positive rate was very low in this study. The possibility of human infection with N. caninum remains to be evaluated further.

Citations

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  • Neospora caninum in pigs and pig farmers in India: Examining the prevalence, immunodominant antigens and associated risk factors
    Veena Mishra, Pallabi Mitra, Shilpshri Shinde, Sandeep Chaudhari, Abhijit S. Deshmukh
    Microbial Pathogenesis.2025; 200: 107352.     CrossRef
  • Molecular Detection of Toxoplasma gondii and Neospora caninum in Naturally Infected sheep, cow, and buffalo Milk
    Tuğçe Tuygun, Serbülent Yiğit, Elif Burcu Gençay Topçu, Şinasi Umur
    Acta Parasitologica.2025;[Epub]     CrossRef
  • Seroprevalences of Toxoplasma gondii and Neospora caninum infections in Jordanian women who had a recent spontaneous abortion
    Mahmoud N. Abo-Shehada, Raida Khalil, Marwan Abu-Halaweh, Kanar Sweis, Zuhair Amr, Lena Billeh
    Revista Brasileira de Parasitologia Veterinária.2021;[Epub]     CrossRef
  • Neosporosis: An Overview of Its Molecular Epidemiology and Pathogenesis
    Asis Khan, Jahangheer S. Shaik, Patricia Sikorski, Jitender P. Dubey, Michael E. Grigg
    Engineering.2020; 6(1): 10.     CrossRef
  • Neospora caninum: a new class of biopharmaceuticals in the therapeutic arsenal against cancer
    Louis Lantier, Agathe Poupée-Beaugé, Anne di Tommaso, Céline Ducournau, Mathieu Epardaud, Zineb Lakhrif, Stéphanie Germon, Françoise Debierre-Grockiego, Marie-Noëlle Mévélec, Arthur Battistoni, Loïs Coënon, Nora Deluce-Kakwata-Nkor, Florence Velge-Roussel
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  • Serological evaluation of Neospora caninum in pregnant women treated at referral center for prenatal screening in Mato Grosso do Sul, Brazil
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  • Toxoplasma gondii-positive human sera recognise intracellular tachyzoites and bradyzoites with diverse patterns of immunoreactivity
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  • Antibodies to Neospora caninum in sheep from slaughterhouses in the state of São Paulo, Brazil
    Laís Moraes Paiz, Rodrigo Costa da Silva, Benedito Donizete Menozzi, Helio Langoni
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  • Neospora caninum and Toxoplasma gondii serodiagnosis in human immunodeficiency virus carriers
    Leandra Marla Oshiro, Ana Rita Coimbra Motta-Castro, Solange Zacalusni Freitas, Rodrigo Casquero Cunha, Rosangela Locatelli Dittrich, Andréa Christine Ferreira Meirelles, Renato Andreotti
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  • Differential susceptibility of human trophoblastic (BeWo) and uterine cervical (HeLa) cells to Neospora caninum infection
    Julianne V. Carvalho, Celene M.O.S. Alves, Mariana R.D. Cardoso, Caroline M. Mota, Bellisa F. Barbosa, Eloísa A.V. Ferro, Neide M. Silva, Tiago W.P. Mineo, José R. Mineo, Deise A.O. Silva
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    Tiago W.P. Mineo, Luciana Benevides, Neide M. Silva, João S. Silva
    Veterinary Research.2009; 40(4): 32.     CrossRef
  • Lack of Serologic Evidence ofNeospora caninumin Humans, England
    Catherine M. McCann, Andrew J. Vyse, Roland L Salmon, Daniel Thomas, Diana J.L. Williams, John W. McGarry, Richard Pebody, Alexander J. Trees
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    B. Moskwa, W. Cabaj
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