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

被引:162
作者
Neelakanta, Girish [1 ]
Sultana, Hameeda [1 ,2 ]
Fish, Durland [3 ]
Anderson, John F. [4 ]
Fikrig, Erol [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Infect Dis Sect, Dept Internal Med, New Haven, CT 06520 USA
[2] Howard Hughes Med Inst, Chevy Chase, MD USA
[3] Yale Univ, Dept Epidemiol & Publ Hlth, Sch Med, New Haven, CT 06520 USA
[4] Connecticut Agr Expt Stn, Dept Entomol, New Haven, CT 06504 USA
关键词
BORRELIA-BURGDORFERI; POLAR FISH; ANTARCTIC FISHES; BABESIA-MICROTI; WINTER ACTIVITY; PROTEINS; ACARI; ICE; IXODIDAE; BIOLOGY;
D O I
10.1172/JCI42868
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:3179 / 3190
页数:12
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