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Hemozoin Pigment: An Important Tool for Low Parasitemic Malarial Diagnosis
Low parasitemic condition in malaria remains a diagnostic challenge; as the available diagnostic methods failed to detect. Currently, hemozoin (Hz) pigment is gaining attention in the diagnosis of malaria. The major drawback is ease of detection of Hz in routine practice. A pilot study was conducted...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Parasitology and Tropical Medicine
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040090/ https://www.ncbi.nlm.nih.gov/pubmed/27658589 http://dx.doi.org/10.3347/kjp.2016.54.4.393 |
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author | Mohapatra, Sarita Ghosh, Arnab Singh, Ruchi Singh, Dhirendra Pratap Sharma, Bhawna Samantaray, Jyotish Chandra Deb, Manorama Gaind, Rajni |
author_facet | Mohapatra, Sarita Ghosh, Arnab Singh, Ruchi Singh, Dhirendra Pratap Sharma, Bhawna Samantaray, Jyotish Chandra Deb, Manorama Gaind, Rajni |
author_sort | Mohapatra, Sarita |
collection | PubMed |
description | Low parasitemic condition in malaria remains a diagnostic challenge; as the available diagnostic methods failed to detect. Currently, hemozoin (Hz) pigment is gaining attention in the diagnosis of malaria. The major drawback is ease of detection of Hz in routine practice. A pilot study was conducted to evaluate the role of Hz pigment and to compare the performance of quantitative buffy coat assay (QBC) and PCR in such conditions. Clinically suspected cases of malaria were examined by both Giemsa stain and immunochromatographic test (ICT). Samples positive by ICT and negative by Giemsa stain were further examined by nested PCR targeting 18S rRNA and QBC for the presence of malaria parasites and pigments. Thirty blood samples fulfilled the inclusion criteria out of which 23 were Plasmodium vivax (Pv), 4 Plasmodium falciparum (Pf), and 3 mixed (Pv and Pf) by immunochromatographic test. Twenty-one out of 30 (70%) were positive by nested PCR in comparison to 25/30 (83%) by QBC. Samples containing both malaria parasites and Hz pigment by QBC completely showed concordance with the PCR result. However, 61% of total samples containing only Hz pigment were observed positive by PCR. Hz pigment remains an important tool for malaria diagnosis. Identification of leukocytes containing pigments by QBC not only indicates recent malarial infections but also puts light on severity of the disease. QBC assay is a rapid, highly sensitive, and cost-effective method to detect malaria parasites and Hz pigment especially in low parasitemic conditions. |
format | Online Article Text |
id | pubmed-5040090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Society for Parasitology and Tropical Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-50400902016-09-29 Hemozoin Pigment: An Important Tool for Low Parasitemic Malarial Diagnosis Mohapatra, Sarita Ghosh, Arnab Singh, Ruchi Singh, Dhirendra Pratap Sharma, Bhawna Samantaray, Jyotish Chandra Deb, Manorama Gaind, Rajni Korean J Parasitol Original Article Low parasitemic condition in malaria remains a diagnostic challenge; as the available diagnostic methods failed to detect. Currently, hemozoin (Hz) pigment is gaining attention in the diagnosis of malaria. The major drawback is ease of detection of Hz in routine practice. A pilot study was conducted to evaluate the role of Hz pigment and to compare the performance of quantitative buffy coat assay (QBC) and PCR in such conditions. Clinically suspected cases of malaria were examined by both Giemsa stain and immunochromatographic test (ICT). Samples positive by ICT and negative by Giemsa stain were further examined by nested PCR targeting 18S rRNA and QBC for the presence of malaria parasites and pigments. Thirty blood samples fulfilled the inclusion criteria out of which 23 were Plasmodium vivax (Pv), 4 Plasmodium falciparum (Pf), and 3 mixed (Pv and Pf) by immunochromatographic test. Twenty-one out of 30 (70%) were positive by nested PCR in comparison to 25/30 (83%) by QBC. Samples containing both malaria parasites and Hz pigment by QBC completely showed concordance with the PCR result. However, 61% of total samples containing only Hz pigment were observed positive by PCR. Hz pigment remains an important tool for malaria diagnosis. Identification of leukocytes containing pigments by QBC not only indicates recent malarial infections but also puts light on severity of the disease. QBC assay is a rapid, highly sensitive, and cost-effective method to detect malaria parasites and Hz pigment especially in low parasitemic conditions. The Korean Society for Parasitology and Tropical Medicine 2016-08 2016-08-31 /pmc/articles/PMC5040090/ /pubmed/27658589 http://dx.doi.org/10.3347/kjp.2016.54.4.393 Text en © 2016, Korean Society for Parasitology and Tropical Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Mohapatra, Sarita Ghosh, Arnab Singh, Ruchi Singh, Dhirendra Pratap Sharma, Bhawna Samantaray, Jyotish Chandra Deb, Manorama Gaind, Rajni Hemozoin Pigment: An Important Tool for Low Parasitemic Malarial Diagnosis |
title | Hemozoin Pigment: An Important Tool for Low Parasitemic Malarial Diagnosis |
title_full | Hemozoin Pigment: An Important Tool for Low Parasitemic Malarial Diagnosis |
title_fullStr | Hemozoin Pigment: An Important Tool for Low Parasitemic Malarial Diagnosis |
title_full_unstemmed | Hemozoin Pigment: An Important Tool for Low Parasitemic Malarial Diagnosis |
title_short | Hemozoin Pigment: An Important Tool for Low Parasitemic Malarial Diagnosis |
title_sort | hemozoin pigment: an important tool for low parasitemic malarial diagnosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040090/ https://www.ncbi.nlm.nih.gov/pubmed/27658589 http://dx.doi.org/10.3347/kjp.2016.54.4.393 |
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