The obligate intracellular pathogen, Anaplasma phagocytophilum, is the causative agent of life-threatening diseases in humans and animals. A. phagocytophilum is an emerging tick-borne pathogen in the United States, Europe, Africa and Asia, with increasing numbers of infected people and animals every year. It is increasingly recognized that intracellular pathogens modify host cell metabolic pathways to increase infection and transmission in both vertebrate and invertebrate hosts. Recent reports have shown that amino acids are central to the host-pathogen metabolic interaction. In this study, a genome-wide search for components of amino acid metabolic pathways was performed in Ixodes scapularis, the main tick vector of A. phagocytophilum in the United States, for which the genome was recently published. The enzymes involved in the synthesis and degradation pathways of the twenty amino acids were identified. Then, the available transcriptomics and proteomics data was used to characterize the mRNA and protein levels of I. scapularis amino acid metabolic pathway components in response to A. phagocytophilum infection of tick tissues and ISE6 tick cells. Our analysis was focused on the interplay between carbohydrate and amino acid metabolism during A. phagocytophilum infection in ISE6 cells. The results showed that tick cells increase the synthesis of phosphoenolpyruvate (PEP) from tyrosine to control A. phagocytophilum infection. Metabolic pathway analysis suggested that this is achieved by (i) increasing the transcript and protein levels of mitochondrial phosphoenolpyruvate carboxykinase (PEPCK-M), (ii) shunting tyrosine into the tricarboxylic acid (TCA) cycle to increase fumarate and oxaloacetate which will be converted into PEP by PEPCK-M, and (iii) blocking all the pathways that use PEP downstream gluconeogenesis (i.e., de novo serine synthesis pathway (SSP), glyceroneogenesis and gluconeogenesis). While sequestering host PEP may be critical for this bacterium because it cannot actively carry out glycolysis to produce PEP, excess of this metabolite may be toxic for A. phagocytophilum. The present work provides a more comprehensive view of the major amino acid metabolic pathways involved in the response to pathogen infection in ticks, and provides the basis for further studies to develop novel strategies for the control of granulocytic anaplasmosis.

• Klíčová slova
• Anaplasma phagocytophilum, Ixodes scapularis, glycerol- 3-phosphate, phosphoenolpyruvate, proteomics, transcriptomics,
• MeSH
• aminokyseliny metabolismus   MeSH
• Anaplasma phagocytophilum účinky léků   genetika   metabolismus   patogenita   MeSH
• anaplasmóza MeSH
• apoptóza MeSH
• bakteriální proteiny genetika   metabolismus   MeSH
• buněčné linie MeSH
• citrátový cyklus MeSH
• fosfoenolpyruvát metabolismus   farmakologie   MeSH
• fosfoenolpyruvátkarboxykinasa (závislá na ATP) metabolismus   MeSH
• genom bakteriální MeSH
• glukoneogeneze MeSH
• glykolýza MeSH
• interakce hostitele a patogenu fyziologie   MeSH
• klíště mikrobiologie   MeSH
• kyselina oxaloctová metabolismus   MeSH
• messenger RNA genetika   MeSH
• metabolické sítě a dráhy genetika   MeSH
• metabolismus sacharidů MeSH
• mitochondrie metabolismus   MeSH
• proteomika metody   MeSH
• serin metabolismus   MeSH
• transkriptom MeSH
• tyrosin metabolismus   MeSH
• zvířata MeSH
• Check Tag
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Názvy látek
• aminokyseliny MeSH
• bakteriální proteiny MeSH
• fosfoenolpyruvát MeSH
• fosfoenolpyruvátkarboxykinasa (závislá na ATP) MeSH
• kyselina oxaloctová MeSH
• messenger RNA MeSH
• serin MeSH
• tyrosin MeSH