scholarly journals Plasmodium sporozoite phospholipid scramblase interacts with mammalian carbamoyl-phosphate synthetase 1 to infect hepatocytes

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Sung-Jae Cha ◽  
Min-Sik Kim ◽  
Chan Hyun Na ◽  
Marcelo Jacobs-Lorena

AbstractAfter inoculation by the bite of an infected mosquito, Plasmodium sporozoites enter the blood stream and infect the liver, where each infected cell produces thousands of merozoites. These in turn, infect red blood cells and cause malaria symptoms. To initiate a productive infection, sporozoites must exit the circulation by traversing the blood lining of the liver vessels after which they infect hepatocytes with unique specificity. We screened a phage display library for peptides that structurally mimic (mimotope) a sporozoite ligand for hepatocyte recognition. We identified HP1 (hepatocyte-binding peptide 1) that mimics a ~50 kDa sporozoite ligand (identified as phospholipid scramblase). Further, we show that HP1 interacts with a ~160 kDa hepatocyte membrane putative receptor (identified as carbamoyl-phosphate synthetase 1). Importantly, immunization of mice with the HP1 peptide partially protects them from infection by the rodent parasite P. berghei. Moreover, an antibody to the HP1 mimotope inhibits human parasite P. falciparum infection of human hepatocytes in culture. The sporozoite ligand for hepatocyte invasion is a potential novel pre-erythrocytic vaccine candidate.

2016 ◽  
Vol 25 (1) ◽  
pp. 3-9
Author(s):  
Uly A. Nikmah ◽  
Ani R. Prijanti ◽  
Sri W.A. Jusman ◽  
Mohamad Sadikin

Background: Urea biosynthesis is a very important process in the liver which needs ATP, CO2 and functional mitochondria or aerobic condition. Liver can adapt to hypoxic condition, generally and locally. This study aimed to analyze the effect of chronic hypoxia on liver urea biosynthesis as indicated by the level and specific activity of mRNA of carbamoyl phosphate synthetase 1 (CPS1), a key enzyme in urea biosynthesis in hypoxic rats.Methods: 20 male Sprague-Dawley rats were placed in hypoxic chamber supplied by a mixture of 10% O2 and 90% N2. Five rats were sacrificed at 1, 3, 5, and 7 days after exposure. Liver homogenates were analyzed for HIF-1 (hypoxia inducible factor-1) by ELISA, CPS1 mRNA by real time RT-PCR and CPS1 enzymatic specific activities by Pierson method. Data were analyzed by ANOVA test and Pearson correlation.Results: The HIF-1 in liver increased significantly, as well as CPS1 mRNA and CPS1 enzymatic activities (p<0.05). There was a strong correlation (r=0.618; p<0.01) between the level of CPS1 mRNA and CPS1 enzymatic activities, moderate correlation between HIF-1 and CPS1 mRNA (r=0.419; p<0.05) but no correlation between HIF-1 and CPS1 enzymatic activities. The study indicated that urea biosynthesis in liver was affected by hypoxia and partially under HIF-1 regulation. The study also found increase of urea and NH3 biosynthesis related to proteolysis as indicated by the decrease of total body weight and liver weight.Conclusion: There was an increase in the expression and specific activities of CPS1 in urea biosynthesis as a result of increasing proteolysis  in chronic hypoxic condition.


2010 ◽  
Vol 393 (1) ◽  
pp. 73-78 ◽  
Author(s):  
Masahito Ogura ◽  
Yasuhiko Nakamura ◽  
Daisuke Tanaka ◽  
Xiaotong Zhuang ◽  
Yoshihito Fujita ◽  
...  

2011 ◽  
Vol 17 (12) ◽  
pp. 1481-1484 ◽  
Author(s):  
Timothy R. Bates ◽  
Barry D. Lewis ◽  
John R. Burnett ◽  
Kenji So ◽  
Andrew Mitchell ◽  
...  

2016 ◽  
Vol 66 (6) ◽  
pp. 333-336
Author(s):  
Maki Yamaguchi ◽  
Tatsuki R. Kataoka ◽  
Takahiro Shibayama ◽  
Akinari Fukuda ◽  
Atsuko Nakazawa ◽  
...  

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