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Enhancing the sensitivity of micro magnetic resonance relaxometry detection of low parasitemia Plasmodium falciparum in human blood.
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- معلومة اضافية
- المصدر:
Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE
- بيانات النشر:
Original Publication: London : Nature Publishing Group, copyright 2011-
- الموضوع:
- نبذة مختصرة :
Upon Plasmodium falciparum infection of the red blood cells (RBCs), the parasite replicates and consumes haemoglobin resulting in the release of free heme which is rapidly converted to hemozoin crystallites. The bulk magnetic susceptibility of infected RBCs (iRBCs) is changed due to ferric (Fe 3+ ) paramagnetic state in hemozoin crystallites which induce a measurable change in spin-spin relaxation (transverse relaxation) rate in proton nuclear magnetic resonance (NMR) of iRBCs. Earlier, our group reported that this transverse relaxation rate (R 2 ) can be measured by an inexpensive, portable 0.5 Tesla bench top magnetic resonance relaxometry (MRR) system with minimum sample preparation and is able to detect very low levels of parasitemia in both blood cultures as well as animal models. However, it was challenging to diagnose malaria in human blood using MRR, mainly due to the inherent variation of R 2 values of clinical blood samples, caused by many physiological and genotypic differences not related to the parasite infection. To resolve the problem of baseline R 2 rates, we have developed an improved lysis protocol for removing confounding molecular and cellular background for MRR detection. With this new protocol and by processing larger volume of blood (>1 ml), we are able to reliably detect very low level of parasitemia (representing early stage of infection, ~0.0001%) with a stable baseline and improved sensitivity using the current MRR system.
- References:
Korean J Parasitol. 2016 Aug;54(4):393-7. (PMID: 27658589)
Am J Trop Med Hyg. 2017 Nov;97(5):1540-1550. (PMID: 28820709)
Sci Rep. 2016 Nov 09;6:36808. (PMID: 27827432)
Science. 1996 Jan 12;271(5246):219-22. (PMID: 8539625)
Magn Reson Med. 1995 Aug;34(2):234-41. (PMID: 7476083)
Nature. 2017 Oct 26;550(7677):515-518. (PMID: 29019978)
Elife. 2015 Jul 14;4:. (PMID: 26173178)
Malar J. 2012 Mar 06;11:64. (PMID: 22394452)
J Exp Med. 1984 Nov 1;160(5):1585-90. (PMID: 6208311)
Clin Microbiol Rev. 2002 Jan;15(1):66-78. (PMID: 11781267)
Korean J Parasitol. 2009 Jun;47(2):93-102. (PMID: 19488414)
Can J Infect Dis Med Microbiol. 2017;2017:9286392. (PMID: 28479922)
Clin Infect Dis. 2011 Jun;52(11):1356-62. (PMID: 21596677)
Mediterr J Hematol Infect Dis. 2012;4(1):e2012073. (PMID: 23205261)
Proc Natl Acad Sci U S A. 2014 Aug 19;111(33):11955-60. (PMID: 25092330)
Biochim Biophys Acta. 2009 Feb;1792(2):93-9. (PMID: 19056489)
Bull World Health Organ. 1988;66(5):621-6. (PMID: 2463112)
J Clin Pathol. 1996 Jul;49(7):533-8. (PMID: 8813948)
Bull World Health Organ. 1982;60(5):755-9. (PMID: 6758971)
Lancet. 2004 Nov 20-26;364(9448):1896-8. (PMID: 15555670)
J Egypt Soc Parasitol. 2016 Apr;46(1):1-8. (PMID: 27363035)
Nat Med. 2014 Sep;20(9):1069-73. (PMID: 25173428)
J Cell Physiol. 1985 Dec;125(3):521-7. (PMID: 2999164)
Sci Rep. 2015 Jun 17;5:11425. (PMID: 26081638)
Malar J. 2016 Jul 12;15(1):358. (PMID: 27405995)
- الموضوع:
Date Created: 20190224 Date Completed: 20200918 Latest Revision: 20240714
- الموضوع:
20240714
- الرقم المعرف:
PMC6385492
- الرقم المعرف:
10.1038/s41598-019-38805-2
- الرقم المعرف:
30796262
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