Literature DB >> 845741

Lipids of Plasmodium lophurae, and of erythrocytes and plasma of normal and P. lophurae-infected Pekin ducklings.

D H Beach, I W Sherman, G G Holz.   

Abstract

A lipid analysis was performed on the avian malaria parasite Plasmodium lophurae, freed from duckling erythrocytes by immune hemolysis, and on the erythrocytes and plasmas of normal and P. lophurae-infected ducklings. Major lipids of normal erythrocytes were: phosphatidylcholine (40% of total lipids), phosphatidylethanolamine (20%), cholesterol (20%), sphingomyelin (11%), and glycosphingolipids (5%). Major fatty acids of erythrocyte total phospholipids (74% of total lipids) were 16:0 (22%), 18:2 (n-6) (21%), 18.1 (n-7, n-9) (18%), 18:0 (9%), 20:4 (n-6) (9%), 22:6 (n-3) (5%). Erythrocyte phosphatidylcholine was greater than 90% the diacyl form, while phosphatidylethanolamine was approximately 44% alkoxy forms and phosphatidylinositol approximately 11% alkoxy forms. Major fatty aldehydes of phosphatidylethanolamine were 16:0 (47%), 18:1 (23%), 18:0 (14%), and 14:0 (12%). The lipid composition of P. lophurae (plus the parasitophorous vacuole membrane) was qualitatively and quantitatively different from that of the duckling erythrocyte in a number of respects. Major lipids were phosphatidylcholine (40%), phosphatidylethanolamine (36%), cholesterol (8%), phosphatidylinostol (4%), 1,2-diacylglycerols (3%), sphingomyelin (2%), and glycosphingolipids (2%). Diphosphatidylglycerol (approximately 1%) was also detected. The major fatty acids of parasite total phospholipids (86% of total lipids) were more saturated than those of the erythrocyte, and octadecenoic acids were notably elevated: 18:1 (33%), 16:0 (26%), 18:0 (16%), 18:2 (12%), 20:4 (3%), and 22:6 (3%). Parasite phosphatidylcholine and phosphatidylethanolamine were greater than 93% the diacyl form and phosphatidylinositol was approximately 25% alkoxy forms. Major fatty aldehydes of the phosphatidylethanolamine were 14:0 (62%), unidentified long chain forms (24%), 16:0 (7%), 18:0 (4%), 18:1 (3%). The lipid composition of the infected erythrocyte reflected the separate contributions of the erythrocyte and parasite. The major lipids of normal duckling plasma were phosphatidylcholine (33%), triacylglycerols (22%), cholesterol esters (20%), cholesterol (12%), phosphatidylethanolamine (5%), and sphingomyelin (2%). The fatty acids of plasma total lipids were 18:1 (26%), 16:0 (26%), 18:2 (12%), 20:4 (12%), 18:0 (9%), 22:6 (3%). Plasma phosphoglycerides were remarkably lower in C18 unsaturated fatty acids and higher in 20:4 than the erythrocyte phosphoglycerides. Infection of ducklings with P. lophurae caused increases in plasma unesterified fatty acids, triacylglycerols and cholesterol esters, and a notable rise in the 18:1 content of all fatty acid-containing plasma neutral lipids. These findings are compared with those reported for other species of Plasmodium infecting other avian and mammalian hosts.

Entities:  

Mesh:

Substances:

Year:  1977        PMID: 845741

Source DB:  PubMed          Journal:  J Parasitol        ISSN: 0022-3395            Impact factor:   1.276


  10 in total

1.  Fluorescence studies on erythrocyte membrane isolated from Plasmodium berghei infected mice.

Authors:  V Koppaka; R Sharma; A K Lala
Journal:  Mol Cell Biochem       Date:  1989 Nov 23-Dec 19       Impact factor: 3.396

Review 2.  Biochemistry of Plasmodium (malarial parasites).

Authors:  I W Sherman
Journal:  Microbiol Rev       Date:  1979-12

3.  Phagosomal membrane lipids of LM fibroblasts.

Authors:  F Schroeder
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

4.  Uninfected red cells from malaria-infected blood: alteration of fatty acid composition involving a serum protein: an in vivo and in vitro study.

Authors:  B D Beaumelle; H J Vial
Journal:  In Vitro Cell Dev Biol       Date:  1988-07

Review 5.  Lipids and the malarial parasite.

Authors:  G G Holz
Journal:  Bull World Health Organ       Date:  1977       Impact factor: 9.408

6.  In vitro production and partial purification of Plasmodium falciparum antigen.

Authors:  W A Siddiqui; S C Kan; K Kramer; S M Richmond-Crum
Journal:  Bull World Health Organ       Date:  1979       Impact factor: 9.408

7.  Lipids from Plasmodium vinckei-infected erythrocytes and their susceptibility to oxidative damage.

Authors:  R Stocker; W B Cowden; R L Tellam; M J Weidemann; N H Hunt
Journal:  Lipids       Date:  1987-01       Impact factor: 1.880

8.  Modulation of Lipoprotein Cholesterol Levels in Plasmodium berghei Malarial Infection by Crude Aqueous Extract of Ganoderma lucidum.

Authors:  Olarewaju M Oluba; Augustine O Olusola; George O Eidangbe; Leye J Babatola; E Chukwu Onyeneke
Journal:  Cholesterol       Date:  2012-07-25

9.  Structural and functional analysis of the pore-forming toxin NetB from Clostridium perfringens.

Authors:  Xu-Xia Yan; Corrine J Porter; Simon P Hardy; David Steer; A Ian Smith; Noelene S Quinsey; Victoria Hughes; Jackie K Cheung; Anthony L Keyburn; Magne Kaldhusdal; Robert J Moore; Trudi L Bannam; James C Whisstock; Julian I Rood
Journal:  mBio       Date:  2013-02-05       Impact factor: 7.867

10.  Lipid traffic between high density lipoproteins and Plasmodium falciparum-infected red blood cells.

Authors:  P Grellier; D Rigomier; V Clavey; J C Fruchart; J Schrevel
Journal:  J Cell Biol       Date:  1991-01       Impact factor: 10.539

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.