Host–parasite interactions that guide red blood cell invasion by malaria parasites. Issue 3 (May 2015)
- Record Type:
- Journal Article
- Title:
- Host–parasite interactions that guide red blood cell invasion by malaria parasites. Issue 3 (May 2015)
- Main Title:
- Host–parasite interactions that guide red blood cell invasion by malaria parasites
- Authors:
- Paul, Aditya S.
Egan, Elizabeth S.
Duraisingh, Manoj T. - Abstract:
- <abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Purpose of review</title> <p>Malaria is caused by the infection and proliferation of parasites from the genus <italic>Plasmodium</italic> in red blood cells (RBCs). A free <italic>Plasmodium</italic> parasite, or merozoite, released from an infected RBC must invade another RBC host cell to sustain a blood-stage infection. Here, we review recent advances on RBC invasion by <italic>Plasmodium</italic> merozoites, focusing on specific molecular interactions between host and parasite.</p> </sec> <sec> <title>Recent findings</title> <p>Recent work highlights the central role of host–parasite interactions at virtually every stage of RBC invasion by merozoites. Biophysical experiments have for the first time measured the strength of merozoite–RBC attachment during invasion. For <italic>P. falciparum</italic>, there have been many key insights regarding the invasion ligand PfRh5 in particular, including its influence on host species tropism, a co-crystal structure with its RBC receptor basigin, and its suitability as a vaccine target. For <italic>P. vivax</italic>, researchers identified the origin and emergence of the parasite from Africa, demonstrating a natural link to the Duffy-negative RBC variant in African populations. For the simian parasite <italic>P. knowlesi</italic>, zoonotic invasion into human cells is linked to RBC age, which has implications for parasitemia during an infection and thus<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Purpose of review</title> <p>Malaria is caused by the infection and proliferation of parasites from the genus <italic>Plasmodium</italic> in red blood cells (RBCs). A free <italic>Plasmodium</italic> parasite, or merozoite, released from an infected RBC must invade another RBC host cell to sustain a blood-stage infection. Here, we review recent advances on RBC invasion by <italic>Plasmodium</italic> merozoites, focusing on specific molecular interactions between host and parasite.</p> </sec> <sec> <title>Recent findings</title> <p>Recent work highlights the central role of host–parasite interactions at virtually every stage of RBC invasion by merozoites. Biophysical experiments have for the first time measured the strength of merozoite–RBC attachment during invasion. For <italic>P. falciparum</italic>, there have been many key insights regarding the invasion ligand PfRh5 in particular, including its influence on host species tropism, a co-crystal structure with its RBC receptor basigin, and its suitability as a vaccine target. For <italic>P. vivax</italic>, researchers identified the origin and emergence of the parasite from Africa, demonstrating a natural link to the Duffy-negative RBC variant in African populations. For the simian parasite <italic>P. knowlesi</italic>, zoonotic invasion into human cells is linked to RBC age, which has implications for parasitemia during an infection and thus malaria.</p> </sec> <sec> <title>Summary</title> <p>New studies of the molecular and cellular mechanisms governing RBC invasion by <italic>Plasmodium</italic> parasites have shed light on various aspects of parasite biology and host cell tropism, and indicate opportunities for malaria control.</p> </sec> </abstract> … (more)
- Is Part Of:
- Current opinion in hematology. Volume 22:Issue 3(2015:May)
- Journal:
- Current opinion in hematology
- Issue:
- Volume 22:Issue 3(2015:May)
- Issue Display:
- Volume 22, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 22
- Issue:
- 3
- Issue Sort Value:
- 2015-0022-0003-0000
- Page Start:
- Page End:
- Publication Date:
- 2015-05
- Subjects:
- Hematology -- Periodicals
Blood -- Diseases -- Periodicals
616.15 - Journal URLs:
- http://journals.lww.com/co-hematology/pages/default.aspx ↗
http://journals.lww.com/pages/default.aspx ↗ - DOI:
- 10.1097/MOH.0000000000000135 ↗
- Languages:
- English
- ISSNs:
- 1065-6251
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3500.775200
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3313.xml