Global host metabolic response to <it>Plasmodium vivax </it>infection: a <sup>1</sup>H NMR based urinary metabonomic study

<p>Abstract</p> <p>Background</p> <p><it>Plasmodium vivax </it>is responsible for the majority of malarial infection in the Indian subcontinent. This species of the parasite is generally believed to cause a relatively benign form of the disease. However, rec...

Full description

Bibliographic Details
Main Authors: Sengupta Arjun, Ghosh Soumita, Basant Angika, Malusare Suhas, Johri Parul, Pathak Sulabha, Sharma Shobhona, Sonawat Haripalsingh M
Format: Article
Language:English
Published: BMC 2011-12-01
Series:Malaria Journal
Subjects:
Online Access:http://www.malariajournal.com/content/10/1/384
_version_ 1828555025835622400
author Sengupta Arjun
Ghosh Soumita
Basant Angika
Malusare Suhas
Johri Parul
Pathak Sulabha
Sharma Shobhona
Sonawat Haripalsingh M
author_facet Sengupta Arjun
Ghosh Soumita
Basant Angika
Malusare Suhas
Johri Parul
Pathak Sulabha
Sharma Shobhona
Sonawat Haripalsingh M
author_sort Sengupta Arjun
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p><it>Plasmodium vivax </it>is responsible for the majority of malarial infection in the Indian subcontinent. This species of the parasite is generally believed to cause a relatively benign form of the disease. However, recent reports from different parts of the world indicate that vivax malaria can also have severe manifestation. Host response to the parasite invasion is thought to be an important factor in determining the severity of manifestation. In this paper, attempt was made to determine the host metabolic response associated with <it>P. vivax </it>infection by means of NMR spectroscopy-based metabonomic techniques in an attempt to better understand the disease pathology.</p> <p>Methods</p> <p>NMR spectroscopy of urine samples from <it>P. vivax-</it>infected patients, healthy individuals and non-malarial fever patients were carried out followed by multivariate statistical analysis. Two data analysis techniques were employed, namely, Principal Component Analysis [PCA] and Orthogonal Projection to Latent Structure Discriminant Analysis [OPLS-DA]. Several NMR signals from the urinary metabolites were further selected for univariate comparison among the classes.</p> <p>Results</p> <p>The urine metabolic profiles of <it>P. vivax-</it>infected patients were distinct from those of healthy individuals as well as of non-malarial fever patients. A highly predictive model was constructed from urine profile of malarial and non-malarial fever patients. Several metabolites were found to be varying significantly across these cohorts. Urinary ornithine seems to have the potential to be used as biomarkers of vivax malaria. An increasing trend in pipecolic acid was also observed. The results suggest impairment in the functioning of liver as well as impairment in urea cycle.</p> <p>Conclusions</p> <p>The results open up a possibility of non-invasive analysis and diagnosis of <it>P. vivax </it>using urine metabolic profile. Distinct variations in certain metabolites were recorded, and amongst these, ornithine may have the potential of being used as biomarker of malaria. Pipecolic acid also showed increasing trend in the malaria patient compared to the other groups.</p>
first_indexed 2024-12-12T05:46:09Z
format Article
id doaj.art-970cdc82ad2448b58e27c5482006e92e
institution Directory Open Access Journal
issn 1475-2875
language English
last_indexed 2024-12-12T05:46:09Z
publishDate 2011-12-01
publisher BMC
record_format Article
series Malaria Journal
spelling doaj.art-970cdc82ad2448b58e27c5482006e92e2022-12-22T00:35:47ZengBMCMalaria Journal1475-28752011-12-0110138410.1186/1475-2875-10-384Global host metabolic response to <it>Plasmodium vivax </it>infection: a <sup>1</sup>H NMR based urinary metabonomic studySengupta ArjunGhosh SoumitaBasant AngikaMalusare SuhasJohri ParulPathak SulabhaSharma ShobhonaSonawat Haripalsingh M<p>Abstract</p> <p>Background</p> <p><it>Plasmodium vivax </it>is responsible for the majority of malarial infection in the Indian subcontinent. This species of the parasite is generally believed to cause a relatively benign form of the disease. However, recent reports from different parts of the world indicate that vivax malaria can also have severe manifestation. Host response to the parasite invasion is thought to be an important factor in determining the severity of manifestation. In this paper, attempt was made to determine the host metabolic response associated with <it>P. vivax </it>infection by means of NMR spectroscopy-based metabonomic techniques in an attempt to better understand the disease pathology.</p> <p>Methods</p> <p>NMR spectroscopy of urine samples from <it>P. vivax-</it>infected patients, healthy individuals and non-malarial fever patients were carried out followed by multivariate statistical analysis. Two data analysis techniques were employed, namely, Principal Component Analysis [PCA] and Orthogonal Projection to Latent Structure Discriminant Analysis [OPLS-DA]. Several NMR signals from the urinary metabolites were further selected for univariate comparison among the classes.</p> <p>Results</p> <p>The urine metabolic profiles of <it>P. vivax-</it>infected patients were distinct from those of healthy individuals as well as of non-malarial fever patients. A highly predictive model was constructed from urine profile of malarial and non-malarial fever patients. Several metabolites were found to be varying significantly across these cohorts. Urinary ornithine seems to have the potential to be used as biomarkers of vivax malaria. An increasing trend in pipecolic acid was also observed. The results suggest impairment in the functioning of liver as well as impairment in urea cycle.</p> <p>Conclusions</p> <p>The results open up a possibility of non-invasive analysis and diagnosis of <it>P. vivax </it>using urine metabolic profile. Distinct variations in certain metabolites were recorded, and amongst these, ornithine may have the potential of being used as biomarker of malaria. Pipecolic acid also showed increasing trend in the malaria patient compared to the other groups.</p>http://www.malariajournal.com/content/10/1/384<it>Plasmodium vivax</it>NMRmetabonomicsmetabolitesbiomarker
spellingShingle Sengupta Arjun
Ghosh Soumita
Basant Angika
Malusare Suhas
Johri Parul
Pathak Sulabha
Sharma Shobhona
Sonawat Haripalsingh M
Global host metabolic response to <it>Plasmodium vivax </it>infection: a <sup>1</sup>H NMR based urinary metabonomic study
Malaria Journal
<it>Plasmodium vivax</it>
NMR
metabonomics
metabolites
biomarker
title Global host metabolic response to <it>Plasmodium vivax </it>infection: a <sup>1</sup>H NMR based urinary metabonomic study
title_full Global host metabolic response to <it>Plasmodium vivax </it>infection: a <sup>1</sup>H NMR based urinary metabonomic study
title_fullStr Global host metabolic response to <it>Plasmodium vivax </it>infection: a <sup>1</sup>H NMR based urinary metabonomic study
title_full_unstemmed Global host metabolic response to <it>Plasmodium vivax </it>infection: a <sup>1</sup>H NMR based urinary metabonomic study
title_short Global host metabolic response to <it>Plasmodium vivax </it>infection: a <sup>1</sup>H NMR based urinary metabonomic study
title_sort global host metabolic response to it plasmodium vivax it infection a sup 1 sup h nmr based urinary metabonomic study
topic <it>Plasmodium vivax</it>
NMR
metabonomics
metabolites
biomarker
url http://www.malariajournal.com/content/10/1/384
work_keys_str_mv AT senguptaarjun globalhostmetabolicresponsetoitplasmodiumvivaxitinfectionasup1suphnmrbasedurinarymetabonomicstudy
AT ghoshsoumita globalhostmetabolicresponsetoitplasmodiumvivaxitinfectionasup1suphnmrbasedurinarymetabonomicstudy
AT basantangika globalhostmetabolicresponsetoitplasmodiumvivaxitinfectionasup1suphnmrbasedurinarymetabonomicstudy
AT malusaresuhas globalhostmetabolicresponsetoitplasmodiumvivaxitinfectionasup1suphnmrbasedurinarymetabonomicstudy
AT johriparul globalhostmetabolicresponsetoitplasmodiumvivaxitinfectionasup1suphnmrbasedurinarymetabonomicstudy
AT pathaksulabha globalhostmetabolicresponsetoitplasmodiumvivaxitinfectionasup1suphnmrbasedurinarymetabonomicstudy
AT sharmashobhona globalhostmetabolicresponsetoitplasmodiumvivaxitinfectionasup1suphnmrbasedurinarymetabonomicstudy
AT sonawatharipalsinghm globalhostmetabolicresponsetoitplasmodiumvivaxitinfectionasup1suphnmrbasedurinarymetabonomicstudy