Literature DB >> 26851675

Soluble recombinant merozoite surface antigen-142kDa of Plasmodium vivax: An improved diagnostic antigen for vivax malaria.

Hadi Mirahmadi1, Shirzad Fallahi2, Seyyed Javad Seyyed Tabaei3.   

Abstract

Enzyme Linked Immunosorbent Assay (ELISA), as a serological test, can be a beneficial tool for epidemiological studies by screening blood donors and diagnosis of specific antibodies from Plasmodium vivax (P. vivax) infected cases. Since P. vivax cannot easily be acquired in vitro, ELISA assays using total or semi-purified antigens are seldom used. On the basis of this restriction, we examined whether recombinant protein 42 kDa related to C-terminal region of the merozoite surface antigen-1 of P. vivax (MSA-1(42)) could be suitable for serological detection of vivax malaria infection. Purified recombinant protein produced in Escherichia coli (E. coli) (GST-MSA-1(42)) was examined for its ability to bind to IgG antibodies of individuals with patent P. vivax infection. The method was tested with 262 serum samples collected from individuals living in the south and southeastern regions of Iran where malaria is endemic. Samples exposed to Plasmodium falciparum (P. falciparum) infection and patients with other infectious disease (toxoplasmosis, Leishmania infantum infection, echinococcosis and FUO (fever with unknown origin)) except for P. falciparum were residing in non- malaria endemic areas in Iran. Generally, the sensitivity of ELISA evaluated with sera from naturally infected individuals was 86.9%. The specificity value of the ELISA determined with sera from healthy individuals and from individuals with other infectious diseases was 94.05%. The positive predictive value (PPV), negative predictive value (NPV) provided, and the diagnostic efficiency of anti-rPvMSA-1(42) antibody using indirect ELISA were determined 93.58, 87.77 and 91.06% respectively. Our study demonstrated that, because MSA-1(42) kDa contains both the 33 and 19 kDa fragments in its structure, it can serve as the basis for the development of a sensitive serological test which can be used for epidemiological studies, screening blood donors and diagnosis of P. vivax malaria.
Copyright © 2016. Published by Elsevier B.V.

Entities:  

Keywords:  ELISA; P. vivax; Recombinant merozoite surface antigen-1; Vivax malaria

Mesh:

Substances:

Year:  2016        PMID: 26851675     DOI: 10.1016/j.mimet.2016.02.003

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  4 in total

1.  Distribution of Antibodies Specific to the 19-kDa and 33-kDa Fragments of Plasmodium vivax Merozoite Surface Protein 1 in Two Pathogenic Strains Infecting Korean Vivax Malaria Patients.

Authors:  Sylvatrie-Danne Dinzouna-Boutamba; Sanghyun Lee; Ui-Han Son; Su-Min Song; Hye Soo Yun; So-Young Joo; Dongmi Kwak; Man Hee Rhee; Dong-Il Chung; Yeonchul Hong; Youn-Kyoung Goo
Journal:  Osong Public Health Res Perspect       Date:  2016-06-25

2.  Sequence Analysis of Pvama-1 among Plasmodium Vivax Isolates in Sistan-Baluchistan.

Authors:  Hadi Mirahmadi; Tahere Safari; Malihe Metanat; Seyed Mehdi Tabatabaei; Ahmad Mehravaran; Saber Raeghi
Journal:  Ethiop J Health Sci       Date:  2020-07-01

3.  Serological responses to a soluble recombinant circumsporozoite protein-VK210 of Plasmodium vivax (rPvCSP-VK210) among Iranian malaria patients.

Authors:  Mehdi Nateghpour; Soudabeh Etemadi; Afsaneh Motevalli Haghi; Hamid Eslami; Mehdi Mohebali; Leila Farivar
Journal:  Eur J Med Res       Date:  2021-11-25       Impact factor: 2.175

4.  Investigation of LAMP Technique in Diagnosis Type of Plasmodium Species in Anopheles Mosquitoes :A Fast and Practical Technique to Detect Malaria Pathogens in the Field.

Authors:  Hadi Mirahmadi; Nadia Kazemipour; Anis Yazdiani; Ahmad Mehravaran; Hamid Reza Basseri; Leili Mohammadi; Ebrahim Alijani
Journal:  Ethiop J Health Sci       Date:  2021-07
  4 in total

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