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Original Article

Molecular Method Confirms Canine Leishmania Infection Detected by Serological Methods in Non-Endemic Area of Brazil
Emeline Riboldi, Flavio Carvalho, Pedro Roosevelt Torres Roma?o, Regina Bones Barcellos, Graziele Lima Bello, Raquel Rocha Ramos, Rosemari Terezinha de Oliveira, Joa?o Pessoa Arau?jo Ju?nior, Maria Lucia Rossetti, Eliane Dallegrave
Korean J Parasitol 2018;56(1):11-19.
Published online February 28, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.1.11
In Brazil, visceral leishmaniasis (VL) is expanding and becoming urbanized, especially in non-endemic areas such as the State of Rio Grande do Sul. Considering that infected dogs are the main reservoir for zoonotic VL, this study evaluated the prevalence of canine visceral leishmaniasis (CVL) in the metropolitan area of Porto Alegre, a new area of ex- pansion of VL in Brazil. Serum and plasma from 405 asymptomatic dogs from the municipalities of Canoas (n = 107), Sa?o Leopoldo (n=216), and Novo Hamburgo (n=82) were tested for CVL using immunochromatographic (DPP®) and ELISA EIE® assays (2 assays officially adopted by the Brazilian government for the diagnosis of CVL) and real-time PCR to con- firm the results. There was no agreement among serological and real-time PCR results, indicating that the Leishmania infection in asymptomatic animals with low parasite load, confirmed by negative parasitological tests (smears and parasite culture), need to be evaluated by molecular methods. The prevalence of LVC in the metropolitan region of Porto Alegre, confirmed by real-time PCR was 4% (5.6% in Canoas and 4.6% in Sa?o Leopoldo). The use of molecular method is essential for accurate diagnosis of CVL, especially in asymptomatic dogs in non-endemic areas.

Citations

Citations to this article as recorded by  Crossref logo
  • qPCR as a Tool for the Diagnosis of Visceral and Cutaneous Leishmaniasis: A Systematic Review and Meta-Analysis
    José Bryan Rihs, Mariana Teixeira Vilela, Janete Soares Coelho dos Santos, Job Alves de Souza Filho, Sérgio Caldas, Rodrigo Souza Leite, Marcos Paulo Gomes Mol
    Acta Parasitologica.2025;[Epub]     CrossRef
  • Global Distribution of Canine Visceral Leishmaniasis and the Role of the Dog in the Epidemiology of the Disease
    Diego Fernandes Vilas-Boas, Eiji Kevin Nakasone Nakasone, Ana Alice Maia Gonçalves, Daniel Ferreira Lair, Diana Souza de Oliveira, Diogo Fonseca Soares Pereira, Geralda Gabriele Silva, Ingrid dos Santos Soares Conrado, Lucilene Aparecida Resende, Maykelin
    Pathogens.2024; 13(6): 455.     CrossRef
  • High-resolution mapping of linear epitopes from LiNTPDase2: Advancing leishmaniasis detection using optimized protein and peptide antigens
    Raissa Barbosa de Castro, João Victor Badaró de Moraes, Anna Cláudia Alves de Souza, Evandro Silva Favarato, Fabiana Azevedo Voorwald, Fabiane Matos dos Santos, Gustavo Costa Bressan, Raphael de Souza Vasconcellos, Juliana Lopes Rangel Fietto
    Diagnostic Microbiology and Infectious Disease.2024; 110(2): 116448.     CrossRef
  • Development and preliminary study of the rLiNTPDase2 rapid test: A lateral flow immunochromatographic assay for Canine Visceral Leishmaniasis
    Raissa Barbosa de Castro, Luma Salgado Leopoldino, João Victor Badaró de Moraes, Gustavo Costa Bressan, Raphael de Souza Vasconcellos, Evandro Silva Favarato, Fabiana Azevedo Voorwald, Juliana Lopes Rangel Fietto
    Veterinary Parasitology.2024; 331: 110299.     CrossRef
  • Identification of infection by Leishmania spp. in wild and domestic animals in Brazil: a systematic review with meta-analysis (2001–2021)
    Fabiana Raquel Ratzlaff, Vanessa Osmari, Daniele da Silva, Jaíne Soares de Paula Vasconcellos, Luciana Pötter, Fagner D’ambroso Fernandes, José Américo de Mello Filho, Sônia de Avila Botton, Fernanda Silveira Flores Vogel, Luís Antônio Sangioni
    Parasitology Research.2023; 122(7): 1605.     CrossRef
  • Dynamics of Leishmania spp. infection in dogs from an unaffected region in transition to a visceral leishmaniasis transmission area, Rio Grande do Sul, Brazil
    Michelli Lopes de Souza, Isac Junior Roman, Ana Paula Gnocato Mortari, Fabiana Raquel Ratzlaff, Renata Dalcol Mazaro, Juliana Felipetto Cargnelutti, Irina Lübeck, Rafael Almeida Fighera, Cinthia Melazzo de Andrade, Sônia de Ávila Botton, Fernanda Silveira
    Parasitology Research.2022; 121(11): 3269.     CrossRef
  • Canine Visceral Leishmaniasis in an Area of Sporadic Transmission in Brazil
    Leandro Machado Borges, Alessandra Gutierrez de Oliveira, Nathália Lopes Fontoura Mateus, Everton Falcão de Oliveira, Aline Etelvina Casaril Arrua, Jucelei de Oliveira Moura Infran, Lucas Bezerra Taketa, Paulo Eduardo de Oliveira Monteiro, Carlos Eurico d
    Vector-Borne and Zoonotic Diseases.2021; 21(7): 539.     CrossRef
  • Investigation of canine visceral leishmaniasis in a non-endemic area in Brazil and the comparison of serological and molecular diagnostic tests
    Anaiá da Paixão Sevá, Ana Pérola Drulla Brandão, Silvia Neri Godoy, Rodrigo Martins Soares, Helio Langoni, Bruna Cristine Rodrigues, Mariana Zanchetta e Gava, Paula Ferraz de Camargo Zanotto, Tatiana Jimenez-Villegas, Roberto Hiramoto, Fernando Ferreira
    Revista da Sociedade Brasileira de Medicina Tropical.2021;[Epub]     CrossRef
  • Improving the serodiagnosis of canine Leishmania infantum infection in geographical areas of Brazil with different disease prevalence
    Laura Ramírez, Luana Dias de Moura, Natalia Lopes Fontoura Mateus, Milene Hoehr de Moraes, Leopoldo Fabrício Marçal do Nascimento, Nailson de Jesus Melo, Lucas Bezerra Taketa, Tatiana Catecati, Samuel G. Huete, Karla Penichet, Eliane Mattos Piranda, Aless
    Parasite Epidemiology and Control.2020; 8: e00126.     CrossRef
  • Canine visceral leishmaniasis in area with recent Leishmania transmission: prevalence, diagnosis, and molecular identification of the infecting species
    Josiane Valadão Lopes, Érika Monteiro Michalsky, Nathália Cristina Lima Pereira, Adão Junior Viana de Paula, Andreza Geisiane Maia Souza, Letícia Cavalari Pinheiro, Ana Cristina Vianna Mariano da Rocha Lima, Daniel Moreira de Avelar, João Carlos França-Si
    Revista da Sociedade Brasileira de Medicina Tropical.2020;[Epub]     CrossRef
  • Canine visceral leishmaniasis: Detection of Leishmania spp. genome in peripheral blood of seropositive dogs by real-time polymerase chain reaction (rt-PCR)
    Fabrício Moreira Monteiro, Amanda Sanchez Machado, Fabiana Rocha-Silva, Cláudia Barbosa Assunção, Cidiane Graciele-Melo, Lourena Emanuele Costa, Aquila Serbate Portela, Eduardo Antonio Ferraz Coelho, Sônia Maria de Figueiredo, Rachel Basques Caligiorne
    Microbial Pathogenesis.2019; 126: 263.     CrossRef
  • PREVALÊNCIA DA LEISHMANIOSE VISCERAL CANINA E COINFECÇÕES EM REGIÃO PERIURBANA NO DISTRITO FEDERAL – BRASIL
    Cassio Ricardo Ribeiro, Carolynne Arruda Gonçalves, Lauricio Monteiro Cruz, Paula Diniz Galera
    Ciência Animal Brasileira.2019;[Epub]     CrossRef
  • Multiplex flow cytometry serology to diagnosis of canine visceral leishmaniasis
    Henrique Gama Ker, Wendel Coura-Vital, Diogo Garcia Valadares, Rodrigo Dian Oliveira Aguiar-Soares, Rory Cristiane Fortes de Brito, Patrícia Sampaio Tavares Veras, Deborah Bittencourt Mothé Fraga, Olindo Assis Martins-Filho, Andréa Teixeira-Carvalho, Alex
    Applied Microbiology and Biotechnology.2019; 103(19): 8179.     CrossRef
  • Natural infection by Leishmania infantum in the Lutzomyia longipalpis population of an endemic coastal area to visceral leishmaniasis in Brazil is not associated with bioclimatic factors
    Tiago Feitosa Mota, Orlando Marcos Farias de Sousa, Yuri de Jesus Silva, Lairton Souza Borja, Bruna Martins Macedo Leite, Manuela da Silva Solcà, Djalma Alves de Melo, Claudia Ida Brodskyn, Edelberto Santos Dias, Patrícia Sampaio Tavares Veras, Deborah Bi
    PLOS Neglected Tropical Diseases.2019; 13(8): e0007626.     CrossRef
  • 10,924 View
  • 234 Download
  • 15 Web of Science
  • Crossref
Brief Communications
Development of Lateral Flow Immunoassay for Antigen Detection in Human Angiostrongylus cantonensis Infection
Mu-Xin Chen, Jia-Xu Chen, Shao-Hong Chen, Da-Na Huang, Lin Ai, Ren-Li Zhang
Korean J Parasitol 2016;54(3):375-380.
Published online June 30, 2016
DOI: https://doi.org/10.3347/kjp.2016.54.3.375
Angiostrongyliasis is difficult to be diagnosed for the reason that no ideal method can be used. Serologic tests require specific equipment and are not always available in poverty-stricken zone and are time-consuming. A lateral flow immunoassay (LFIA) may be useful for angiostrongyliasis control. We established a LFIA for the diagnosis of angiostrongyliasis based on 2 monoclonal antibodies (mAbs) against antigens of Angiostrongylus cantonensis adults. The sensitivity and specificity were 91.1% and 100% in LFIA, while those of commercial ELISA kit was 97.8% and 86.3%, respectively. Youden index was 0.91 in LFIA and 0.84 in commercial ELISA kit. LFIA showed detection limit of 1 ng/ml of A. cantonensis ES antigens. This LFIA was simple, rapid, highly sensitive and specific, which opened an alternative approach for the diagnosis of human angiostrongyliasis.

Citations

Citations to this article as recorded by  Crossref logo
  • Rapid Single-Step Immunochromatographic Assay for Angiostrongylus cantonensis Specific Antigen Detection
    Praphathip Eamsobhana, Anchalee Tungtrongchitr, Darawan Wanachiwanawin, Sudarat Boonyong, Hoi-Sen Yong
    Pathogens.2023; 12(6): 762.     CrossRef
  • Semi-Automated Microfluidic Device Combined with a MiniPCR-Duplex Lateral Flow Dipstick for Screening and Visual Species Identification of Lymphatic Filariae
    Achinya Phuakrod, Navapon Kusuwan, Witsaroot Sripumkhai, Pattaraluck Pattamang, Sirichit Wongkamchai
    Micromachines.2022; 13(2): 336.     CrossRef
  • Further studies of neuroangiostrongyliasis (rat lungworm disease) in Australian dogs: 92 new cases (2010–2020) and results for a novel, highly sensitive qPCR assay
    Rogan Lee, Tsung-Yu Pai, Richard Churcher, Sarah Davies, Jody Braddock, Michael Linton, Jane Yu, Erin Bell, Justin Wimpole, Anna Dengate, David Collins, Narelle Brown, George Reppas, Susan Jaensch, Matthew K. Wun, Patricia Martin, William Sears, Jan Šlape
    Parasitology.2021; 148(2): 178.     CrossRef
  • Sandwich dot-immunogold filtration assay (DIGFA) for specific immunodiagnosis of active neuroangiostrongyliasis
    Praphathip Eamsobhana, Anchalee Tungtrongchitr, Hoi-Sen Yong, Anchana Prasartvit, Darawan Wanachiwanawin, Xiao-Xian Gan
    Parasitology.2021; 148(2): 234.     CrossRef
  • Development of a recombinase polymerase amplification (RPA-EXO) and lateral flow assay (RPA-LFA) based on the ITS1 gene for the detection of Angiostrongylus cantonensis in gastropod intermediate hosts
    Susan I. Jarvi, Elizabeth S. Atkinson, Lisa M. Kaluna, Kirsten A. Snook, Argon Steel
    Parasitology.2021; 148(2): 251.     CrossRef
  • Genetic Characterization and Detection of Angiostrongylus cantonensis by Molecular Approaches
    Muxin Chen, Dana Huang, Jiaxu Chen, Yalan Huang, Huiwen Zheng, Yijun Tang, Qian Zhang, Shaohong Chen, Lin Ai, Xiaonong Zhou, Renli Zhang
    Vector-Borne and Zoonotic Diseases.2021; 21(9): 643.     CrossRef
  • Meningitis patients with Angiostrongylus cantonensis may present without eosinophilia in the cerebrospinal fluid in northern Vietnam
    Tomoko Hiraoka, Ngo Chi Cuong, Sugihiro Hamaguchi, Mihoko Kikuchi, Shungo Katoh, Le Kim Anh, Nguyen Thi Hien Anh, Dang Duc Anh, Chris Smith, Haruhiko Maruyama, Lay-Myint Yoshida, Do Duy Cuong, Pham Thanh Thuy, Koya Ariyoshi, Alessandra Morassutti
    PLOS Neglected Tropical Diseases.2020; 14(12): e0008937.     CrossRef
  • Rapid diagnosis of parasitic diseases: current scenario and future needs
    S. Momčilović, C. Cantacessi, V. Arsić-Arsenijević, D. Otranto, S. Tasić-Otašević
    Clinical Microbiology and Infection.2019; 25(3): 290.     CrossRef
  • Diagnostic approach to encephalitis and meningoencephalitis in adult returning travellers
    A. Kenfak, G. Eperon, M. Schibler, F. Lamoth, M.I. Vargas, J.P. Stahl
    Clinical Microbiology and Infection.2019; 25(4): 415.     CrossRef
  • Survey of Angiostrongylus cantonensis Infection Status in Host Animals and Populations in Shenzhen, 2016–2017
    Dana Huang, Yalan Huang, Yijun Tang, Qian Zhang, Xiaoheng Li, Shitong Gao, Wuwei Hua, Renli Zhang
    Vector-Borne and Zoonotic Diseases.2019; 19(10): 717.     CrossRef
  • Immunochromatographic test for rapid serological diagnosis of human angiostrongyliasis
    Praphathip Eamsobhana, Anchalee Tungtrongchitr, Darawan Wanachiwanawin, Hoi-Sen Yong
    International Journal of Infectious Diseases.2018; 73: 69.     CrossRef
  • Small-scale spatial analysis of intermediate and definitive hosts of Angiostrongylus cantonensis
    Qiu-An Hu, Yi Zhang, Yun-Hai Guo, Shan Lv, Shang Xia, He-Xiang Liu, Yuan Fang, Qin Liu, Dan Zhu, Qi-Ming Zhang, Chun-Li Yang, Guang-Yi Lin
    Infectious Diseases of Poverty.2018;[Epub]     CrossRef
  • Current Trends in Ligand Binding Real-Time Measurement Technologies
    Stephanie Fraser, Judy Y. Shih, Mark Ware, Edward O’Connor, Mark J. Cameron, Martin Schwickart, Xuemei Zhao, Karin Regnstrom
    The AAPS Journal.2017; 19(3): 682.     CrossRef
  • 10,711 View
  • 158 Download
  • 14 Web of Science
  • Crossref
Development of a Disperse Dye Immunoassay Technique for Detection of Antibodies against Neospora caninum in Cattle
Fatemeh Selahi, Mehdi Namavari, Mohammad Hossein Hosseini, Maryam Mansourian, Yahya Tahamtan
Korean J Parasitol 2013;51(1):129-132.
Published online February 18, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.1.129

In this study a disperse dye immunoassay method was standardized and evaluated for detection of antibodies against Neospora caninum in cattle. Sera from 150 cattle with a recent history of abortion were collected and tested by commercial ELISA kit and a standardized in-house dye immunoassay system. The positivity rate for the sera used in this study was 34.6% for the disperse dye immunoassay (DDIA) compared to 32% obtained by ELISA kit. This study showed no significant difference between DDIA and ELISA. The results indicated that the DDIA provide an economic, simple, rapid and robust test for detection of N. caninum infection in cattle.

Citations

Citations to this article as recorded by  Crossref logo
  • A novel immunochromatographic assay using ultramarine blue particles as visible label for quantitative detection of hepatitis B virus surface antigen
    Jing Liu, Qiongqiong Yu, Guangying Zhao, Wenchao Dou
    Analytica Chimica Acta.2020; 1098: 140.     CrossRef
  • Review on the immunological and molecular diagnosis of neosporosis (years 2011–2016)
    Francine Alves Sinnott, Leonardo Garcia Monte, Thaís Farias Collares, Roberta Maraninchi Silveira, Sibele Borsuk
    Veterinary Parasitology.2017; 239: 19.     CrossRef
  • Markers related to the diagnosis and to the risk of abortion in bovine neosporosis
    Sonia Almería, Fernando López-Gatius
    Research in Veterinary Science.2015; 100: 169.     CrossRef
  • 8,314 View
  • 71 Download
  • Crossref