z-logo
open-access-imgOpen Access
Malaria Pathogenesis
Author(s) -
Danny A. Milner
Publication year - 2017
Publication title -
cold spring harbor perspectives in medicine
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 3.853
H-Index - 105
eISSN - 2472-5412
pISSN - 2157-1422
DOI - 10.1101/cshperspect.a025569
Subject(s) - plasmodium knowlesi , malaria , plasmodium falciparum , biology , plasmodium (life cycle) , plasmodium malariae , plasmodium vivax , plasmodium ovale , virology , population , immunology , parasite hosting , disease , medicine , pathology , environmental health , world wide web , computer science
In the mosquito-human life cycle, the six species of malaria parasites infecting humans ( Plasmodium falciparum , Plasmodium vivax , Plasmodium ovale wallickeri , Plasmodium ovale curtisi , Plasmodium malariae , and Plasmodium knowlesi ) undergo 10 or more morphological states, replicate from single to 10,000+ cells, and vary in total population from one to many more than 10 6 organisms. In the human host, only a small number of these morphological stages lead to clinical disease and the vast majority of all malaria-infected patients in the world produce few (if any) symptoms in the human. Human clinical disease (e.g., fever, anemia, coma) is the result of the parasite preprogrammed biology in concert with the human pathophysiological response. Caveats and corollaries that add variation to this host-parasite interaction include parasite genetic diversity of key proteins, coinfections, comorbidities, delays in treatment, human polymorphisms, and environmental determinants.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom