Improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice

Abstract Background Despite intensive research, malaria remains a major health concern for non-immune residents and travelers in malaria-endemic regions. Efficient adjunctive therapies against life-threatening complications such as severe malarial anaemia, encephalopathy, placental malaria or respir...

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Published in:Malaria Journal
Main Authors: Deroost Katrien, Lays Natacha, Noppen Sam, Martens Erik, Opdenakker Ghislain, Van den Steen Philippe E
Format: Article in Journal/Newspaper
Language:English
Published: BMC 2012
Subjects:
Online Access:https://doi.org/10.1186/1475-2875-11-166
https://doaj.org/article/fb3a1d7b9ecc43ccacaeb925cb6e725d
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spelling ftdoajarticles:oai:doaj.org/article:fb3a1d7b9ecc43ccacaeb925cb6e725d 2023-05-15T15:16:03+02:00 Improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice Deroost Katrien Lays Natacha Noppen Sam Martens Erik Opdenakker Ghislain Van den Steen Philippe E 2012-05-01T00:00:00Z https://doi.org/10.1186/1475-2875-11-166 https://doaj.org/article/fb3a1d7b9ecc43ccacaeb925cb6e725d EN eng BMC http://www.malariajournal.com/content/11/1/166 https://doaj.org/toc/1475-2875 doi:10.1186/1475-2875-11-166 1475-2875 https://doaj.org/article/fb3a1d7b9ecc43ccacaeb925cb6e725d Malaria Journal, Vol 11, Iss 1, p 166 (2012) Chemo-luminescence Densitometry Haemozoin quantification Malaria pigment Plasmodium Arctic medicine. Tropical medicine RC955-962 Infectious and parasitic diseases RC109-216 article 2012 ftdoajarticles https://doi.org/10.1186/1475-2875-11-166 2022-12-31T08:10:20Z Abstract Background Despite intensive research, malaria remains a major health concern for non-immune residents and travelers in malaria-endemic regions. Efficient adjunctive therapies against life-threatening complications such as severe malarial anaemia, encephalopathy, placental malaria or respiratory problems are still lacking. Therefore, new insights into the pathogenesis of severe malaria are imperative. Haemozoin (Hz) or malaria pigment is produced during intra-erythrocytic parasite replication, released in the circulation after schizont rupture and accumulates inside multiple organs. Many in vitro and ex vivo immunomodulating effects are described for Hz but in vivo data are limited. This study aimed to improve methods for Hz quantification in tissues and to investigate the accumulation of Hz in different organs from mice infected with Plasmodium parasites with a varying degree of virulence. Methods An improved method for extraction of Hz from tissues was elaborated and coupled to an optimized, quantitative, microtiter plate-based luminescence assay with a high sensitivity. In addition, a technique for measuring Hz by semi-quantitative densitometry, applicable on transmitted light images, was developed. The methods were applied to measure Hz in various organs of C57BL/6 J mice infected with Plasmodium berghei ANKA, P. berghei NK65 or Plasmodium chabaudi AS. The used statistical methods were the Mann–Whitney U test and Pearsons correlation analysis. Results Most Hz was detected in livers and spleens, lower levels in lungs and kidneys, whereas sub-nanomolar amounts were observed in brains and hearts from infected mice, irrespectively of the parasite strain used. Furthermore, total Hz contents correlated with peripheral parasitaemia and were significantly higher in mice with a lethal P. berghei ANKA or P. berghei NK65-infection than in mice with a self-resolving P. chabaudi AS-infection, despite similar peripheral parasitaemia levels. Conclusions The developed techniques were useful to quantify Hz in ... Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Malaria Journal 11 1 166
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Chemo-luminescence
Densitometry
Haemozoin quantification
Malaria pigment
Plasmodium
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
spellingShingle Chemo-luminescence
Densitometry
Haemozoin quantification
Malaria pigment
Plasmodium
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
Deroost Katrien
Lays Natacha
Noppen Sam
Martens Erik
Opdenakker Ghislain
Van den Steen Philippe E
Improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice
topic_facet Chemo-luminescence
Densitometry
Haemozoin quantification
Malaria pigment
Plasmodium
Arctic medicine. Tropical medicine
RC955-962
Infectious and parasitic diseases
RC109-216
description Abstract Background Despite intensive research, malaria remains a major health concern for non-immune residents and travelers in malaria-endemic regions. Efficient adjunctive therapies against life-threatening complications such as severe malarial anaemia, encephalopathy, placental malaria or respiratory problems are still lacking. Therefore, new insights into the pathogenesis of severe malaria are imperative. Haemozoin (Hz) or malaria pigment is produced during intra-erythrocytic parasite replication, released in the circulation after schizont rupture and accumulates inside multiple organs. Many in vitro and ex vivo immunomodulating effects are described for Hz but in vivo data are limited. This study aimed to improve methods for Hz quantification in tissues and to investigate the accumulation of Hz in different organs from mice infected with Plasmodium parasites with a varying degree of virulence. Methods An improved method for extraction of Hz from tissues was elaborated and coupled to an optimized, quantitative, microtiter plate-based luminescence assay with a high sensitivity. In addition, a technique for measuring Hz by semi-quantitative densitometry, applicable on transmitted light images, was developed. The methods were applied to measure Hz in various organs of C57BL/6 J mice infected with Plasmodium berghei ANKA, P. berghei NK65 or Plasmodium chabaudi AS. The used statistical methods were the Mann–Whitney U test and Pearsons correlation analysis. Results Most Hz was detected in livers and spleens, lower levels in lungs and kidneys, whereas sub-nanomolar amounts were observed in brains and hearts from infected mice, irrespectively of the parasite strain used. Furthermore, total Hz contents correlated with peripheral parasitaemia and were significantly higher in mice with a lethal P. berghei ANKA or P. berghei NK65-infection than in mice with a self-resolving P. chabaudi AS-infection, despite similar peripheral parasitaemia levels. Conclusions The developed techniques were useful to quantify Hz in ...
format Article in Journal/Newspaper
author Deroost Katrien
Lays Natacha
Noppen Sam
Martens Erik
Opdenakker Ghislain
Van den Steen Philippe E
author_facet Deroost Katrien
Lays Natacha
Noppen Sam
Martens Erik
Opdenakker Ghislain
Van den Steen Philippe E
author_sort Deroost Katrien
title Improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice
title_short Improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice
title_full Improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice
title_fullStr Improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice
title_full_unstemmed Improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice
title_sort improved methods for haemozoin quantification in tissues yield organ-and parasite-specific information in malaria-infected mice
publisher BMC
publishDate 2012
url https://doi.org/10.1186/1475-2875-11-166
https://doaj.org/article/fb3a1d7b9ecc43ccacaeb925cb6e725d
geographic Arctic
geographic_facet Arctic
genre Arctic
genre_facet Arctic
op_source Malaria Journal, Vol 11, Iss 1, p 166 (2012)
op_relation http://www.malariajournal.com/content/11/1/166
https://doaj.org/toc/1475-2875
doi:10.1186/1475-2875-11-166
1475-2875
https://doaj.org/article/fb3a1d7b9ecc43ccacaeb925cb6e725d
op_doi https://doi.org/10.1186/1475-2875-11-166
container_title Malaria Journal
container_volume 11
container_issue 1
container_start_page 166
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