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Anaplasma phagocytophilum induces Ixodes scapularis ticks to express an antifreeze glycoprotein gene that enhances their survival in the cold
Girish Neelakanta, … , John F. Anderson, Erol Fikrig
Girish Neelakanta, … , John F. Anderson, Erol Fikrig
Published August 25, 2010
Citation Information: J Clin Invest. 2010;120(9):3179-3190. https://doi.org/10.1172/JCI42868.
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Research Article

Anaplasma phagocytophilum induces Ixodes scapularis ticks to express an antifreeze glycoprotein gene that enhances their survival in the cold

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Abstract

In the United States, Ixodes scapularis ticks overwinter in the Northeast and Upper Midwest and transmit the agent of human granulocytic anaplasmosis, Anaplasma phagocytophilum, among other pathogens. We now show that the presence of A. phagocytophilum in I. scapularis ticks increases their ability to survive in the cold. We identified an I. scapularis antifreeze glycoprotein, designated IAFGP, and demonstrated via RNAi knockdown studies the importance of IAFGP for the survival of I. scapularis ticks in a cold environment. Transfection studies also show that IAFGP increased the viability of yeast cells subjected to cold temperature. Remarkably, A. phagocytophilum induced the expression of iafgp, thereby increasing the cold tolerance and survival of I. scapularis. These data define a molecular basis for symbiosis between a human pathogenic bacterium and its arthropod vector and delineate what we believe to be a new pathway that may be targeted to alter the life cycle of this microbe and its invertebrate host.

Authors

Girish Neelakanta, Hameeda Sultana, Durland Fish, John F. Anderson, Erol Fikrig

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Figure 3

Nucleotide and predicted amino acid sequence of IAFGP.

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Nucleotide and predicted amino acid sequence of IAFGP.
The nucleotide se...
The nucleotide sequence of the iafgp gene was obtained by sequencing PCR product cloned in the pGEMT-Easy Vector. The deduced amino acid sequence is shown as a single letter below the nucleotide sequence. The in-frame putative IAFGP translational start and stop codons are indicated in bold. The amino acid sequence corresponding to N-terminal signal peptide is boxed (solid line). Ala-Ala-Thr repeats are underlined, and several O-glycosylation sites are indicated by asterisks. Upstream nucleotide sequence obtained from sequencing additional cDNA clone is shown in lower case. The Kozak sequence at 5′ end and polyadenylation signal at 3′ end are indicated in bold letters and enclosed in dashed boxes.

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