Mechanisms of Obligatory Intracellular Infection with Anaplasma phagocytophilum

<jats:title>SUMMARY</jats:title><jats:p><jats:named-content content-type="genus-species">Anaplasma phagocytophilum</jats:named-content>persists in nature by cycling between mammals and ticks. Human infection by the bite of an infected tick leads to a potentially fatal emerging disease called human granulocytic anaplasmosis.<jats:named-content content-type="genus-species">A. phagocytophilum</jats:named-content>is an obligatory intracellular bacterium that replicates inside mammalian granulocytes and the salivary gland and midgut cells of ticks.<jats:named-content content-type="genus-species">A. phagocytophilum</jats:named-content>evolved the remarkable ability to hijack the regulatory system of host cells.<jats:named-content content-type="genus-species">A. phagocytophilum</jats:named-content>alters vesicular traffic to create an intracellular membrane-bound compartment that allows replication in seclusion from lysosomes. The bacterium downregulates or actively inhibits a number of innate immune responses of mammalian host cells, and it upregulates cellular cholesterol uptake to acquire cholesterol for survival. It also upregulates several genes critical for the infection of ticks, and it prolongs tick survival at freezing temperatures. Several host factors that exacerbate infection have been identified, including interleukin-8 (IL-8) and cholesterol. Host factors that overcome infection include IL-12 and gamma interferon (IFN-γ). Two bacterial type IV secretion effectors and several bacterial proteins that associate with inclusion membranes have been identified. An understanding of the molecular mechanisms underlying<jats:named-content content-type="genus-species">A. phagocytophilum</jats:named-content>infection will foster the development of creative ideas to prevent or treat this emerging tick-borne disease.</jats:p>