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Detection of Ascaris lumbricoides infection by ABA-1 coproantigen ELISA

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Abstract
Intestinal worms, or soil-transmitted helminths (STHs), affect hundreds of millions of people in all tropical and subtropical regions of the world. The most prevalent STH isAscaris lumbricoides. Through large-scale deworming programs, World Health Organization aims to reduce morbidity, caused by moderate-to-heavy intensity infections, below 2%. In order to monitor these control programs, stool samples are examined microscopically for the presence of worm eggs. This procedure requires well-trained personnel and is known to show variability between different operators interpreting the slides. We have investigated whether ABA-1, one of the excretory-secretory products ofA.lumbricoidescan be used as a coproantigen marker for infection with this parasite. Polyclonal antibodies were generated and a coproantigen ELISA was developed. Using this ELISA, it was found that ABA-1 in stool detectedAscarisinfection with a sensitivity of 91.5% and a specificity of 95.3%. Our results also demonstrate that there is a correlation between ABA-1 levels in stool andA.lumbricoidesDNA detected in stool. Using a threshold of 18.2 ng/g stool the ABA-1 ELISA correctly assigned 68.4% of infected individuals to the moderate-to-heavy intensity infection group, with a specificity of 97.1%. Furthermore, the levels of ABA-1 in stool were shown to rapidly and strongly decrease upon administration of a standard anthelminthic treatment (single oral dose of 400 mg albendazole). In anAscaris suuminfection model in pigs, it was found that ABA-1 remained undetectable until day 28 and was detected at day 42 or 56, concurrent with the appearance of worm eggs in the stool. This report demonstrates that ABA-1 can be considered anAscaris-specific coproantigen marker that can be used to monitor infection intensity. It also opens the path for development of point-of-care immunoassay-based tests to determineA.lumbricoidesinfection in stool at the sample collection site. Author summary Intestinal worms are one of the most common infections in tropical and subtropical parts of the world. The roundwormAscaris lumbricoidesis the most prevalent and efforts are ongoing to use preventive chemotherapy to reduce both prevalence and intensity of this infection. To monitor these programs, stool-based microscopy is currently used. We have investigated the possibility of using ABA-1, an abundantly secreted protein from the worm, as a biomarker in stool of infected individuals. We have developed an ELISA and using this assay determined that ABA-1 as stool biomarker had a sensitivity of 91.5% and a specificity of 95.3% to detect infection withA.lumbricoides. We also showed that ABA-1 in stool rapidly and strongly decreased upon administration of a standard anthelminthic treatment. The main asset of this novel stool biomarker is its potential to be used in of point-of-care immunoassay-based tests to determineA.lumbricoidesinfection in stool at the sample collection site.
Keywords
TRANSMITTED HELMINTH INFECTIONS, SUUM, ALLERGEN, ALBENDAZOLE, PIGS, DIAGNOSIS, EFFICACY, ASSAY

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MLA
Lagatie, Ole, et al. “Detection of Ascaris Lumbricoides Infection by ABA-1 Coproantigen ELISA.” PLOS NEGLECTED TROPICAL DISEASES, vol. 14, no. 10, 2020, doi:10.1371/journal.pntd.0008807.
APA
Lagatie, O., Verheyen, A., Van Hoof, K., Lauwers, D., Odiere, M. R., Vlaminck, J., … Stuyver, L. J. (2020). Detection of Ascaris lumbricoides infection by ABA-1 coproantigen ELISA. PLOS NEGLECTED TROPICAL DISEASES, 14(10). https://doi.org/10.1371/journal.pntd.0008807
Chicago author-date
Lagatie, Ole, Ann Verheyen, Kim Van Hoof, Dax Lauwers, Maurice R. Odiere, Johnny Vlaminck, Bruno Levecke, and Lieven J. Stuyver. 2020. “Detection of Ascaris Lumbricoides Infection by ABA-1 Coproantigen ELISA.” PLOS NEGLECTED TROPICAL DISEASES 14 (10). https://doi.org/10.1371/journal.pntd.0008807.
Chicago author-date (all authors)
Lagatie, Ole, Ann Verheyen, Kim Van Hoof, Dax Lauwers, Maurice R. Odiere, Johnny Vlaminck, Bruno Levecke, and Lieven J. Stuyver. 2020. “Detection of Ascaris Lumbricoides Infection by ABA-1 Coproantigen ELISA.” PLOS NEGLECTED TROPICAL DISEASES 14 (10). doi:10.1371/journal.pntd.0008807.
Vancouver
1.
Lagatie O, Verheyen A, Van Hoof K, Lauwers D, Odiere MR, Vlaminck J, et al. Detection of Ascaris lumbricoides infection by ABA-1 coproantigen ELISA. PLOS NEGLECTED TROPICAL DISEASES. 2020;14(10).
IEEE
[1]
O. Lagatie et al., “Detection of Ascaris lumbricoides infection by ABA-1 coproantigen ELISA,” PLOS NEGLECTED TROPICAL DISEASES, vol. 14, no. 10, 2020.
@article{8697675,
  abstract     = {{Intestinal worms, or soil-transmitted helminths (STHs), affect hundreds of millions of people in all tropical and subtropical regions of the world. The most prevalent STH isAscaris lumbricoides. Through large-scale deworming programs, World Health Organization aims to reduce morbidity, caused by moderate-to-heavy intensity infections, below 2%. In order to monitor these control programs, stool samples are examined microscopically for the presence of worm eggs. This procedure requires well-trained personnel and is known to show variability between different operators interpreting the slides. We have investigated whether ABA-1, one of the excretory-secretory products ofA.lumbricoidescan be used as a coproantigen marker for infection with this parasite. Polyclonal antibodies were generated and a coproantigen ELISA was developed. Using this ELISA, it was found that ABA-1 in stool detectedAscarisinfection with a sensitivity of 91.5% and a specificity of 95.3%. Our results also demonstrate that there is a correlation between ABA-1 levels in stool andA.lumbricoidesDNA detected in stool. Using a threshold of 18.2 ng/g stool the ABA-1 ELISA correctly assigned 68.4% of infected individuals to the moderate-to-heavy intensity infection group, with a specificity of 97.1%. Furthermore, the levels of ABA-1 in stool were shown to rapidly and strongly decrease upon administration of a standard anthelminthic treatment (single oral dose of 400 mg albendazole). In anAscaris suuminfection model in pigs, it was found that ABA-1 remained undetectable until day 28 and was detected at day 42 or 56, concurrent with the appearance of worm eggs in the stool. This report demonstrates that ABA-1 can be considered anAscaris-specific coproantigen marker that can be used to monitor infection intensity. It also opens the path for development of point-of-care immunoassay-based tests to determineA.lumbricoidesinfection in stool at the sample collection site. Author summary Intestinal worms are one of the most common infections in tropical and subtropical parts of the world. The roundwormAscaris lumbricoidesis the most prevalent and efforts are ongoing to use preventive chemotherapy to reduce both prevalence and intensity of this infection. To monitor these programs, stool-based microscopy is currently used. We have investigated the possibility of using ABA-1, an abundantly secreted protein from the worm, as a biomarker in stool of infected individuals. We have developed an ELISA and using this assay determined that ABA-1 as stool biomarker had a sensitivity of 91.5% and a specificity of 95.3% to detect infection withA.lumbricoides. We also showed that ABA-1 in stool rapidly and strongly decreased upon administration of a standard anthelminthic treatment. The main asset of this novel stool biomarker is its potential to be used in of point-of-care immunoassay-based tests to determineA.lumbricoidesinfection in stool at the sample collection site.}},
  articleno    = {{e0008807}},
  author       = {{Lagatie, Ole and Verheyen, Ann and Van Hoof, Kim and Lauwers, Dax and Odiere, Maurice R. and Vlaminck, Johnny and Levecke, Bruno and Stuyver, Lieven J.}},
  issn         = {{1935-2735}},
  journal      = {{PLOS NEGLECTED TROPICAL DISEASES}},
  keywords     = {{TRANSMITTED HELMINTH INFECTIONS,SUUM,ALLERGEN,ALBENDAZOLE,PIGS,DIAGNOSIS,EFFICACY,ASSAY}},
  language     = {{eng}},
  number       = {{10}},
  pages        = {{14}},
  title        = {{Detection of Ascaris lumbricoides infection by ABA-1 coproantigen ELISA}},
  url          = {{http://doi.org/10.1371/journal.pntd.0008807}},
  volume       = {{14}},
  year         = {{2020}},
}

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