Since the sequence covered by HB 219 is considerably longer than the MFK motif that defines cysPoLV group 1 var CP673451 price genes, it is likely that HB 219 covers additional sequence variation that is either directly or indirectly linked to

the rosetting phenotype. Furthermore, HB 219 expression correlates with both high parasitemia and hypoglycemia (Figure  3B). Both of these associations further support the hypothesis that HB 219 is linked to a form of severe disease that manifests through overall high parasite burden rather than through tissue-specific sequestration. Within the Kenyan population that is the focus of this study, HB expression rates (and to an even greater extent, PCs of HB expression rate profiles) improve our ability to differentiate mild versus severe spectrum var genes beyond what is possible with classic typing methods. Furthermore, HBs appear to be informative markers of disease phenotype in more than just this particular population. In a dataset from Mali we again find that HB 219 expression is significantly associated with high levels of rosetting, and that the HB composition of the expressed var sequence tags—particularly with

respect to HB 36—predicts disease severity with higher precision, accuracy and recall than classic methods. These results SGC-CBP30 datasheet suggest that the DBLα HB-phenotype associations, which we characterized using the large Kenyan dataset, are consistent across distinct populations. Thus, a single set of DBLα HBs can potentially serve as parasite genetic markers for severe disease phenotypes in geographically diverse populations.

Moreover, the fact that many of the same HB-phenotype relationships are found in two geographically distant populations supports the idea that there is a functional link between particular DBLα HBs and the molecular mechanisms underlying severe disease, since otherwise we would expect recombination to alter HB-phenotype linkages. In summary, HB typing check details methods allow for the construction of more specific genotype-phenotype models that in turn suggest that two distinct molecular mechanisms underlie severe malaria. Specifically, we find that var DBLα HB 204 expression predicts a form of severe disease that is associated with impaired consciousness and the absence Tolmetin of rosetting, and that var DBLα HB 219 expression predicts a form of severe disease that is associated with high rosetting. Insights into genotype-phenotype associations within this system can potentially aid in the development of new diagnostic and monitoring tools for malaria, and perhaps even future vaccines, since var genes have been implicated as possible future vaccine targets [33]. Furthermore, if additional studies are undertaken that assess both var expression and clinical symptoms, it should be possible to further refine our descriptions of these genotype-phenotype relationships.