Arthropod-borne diseases are becoming increasingly prevalent across the globe, and an understanding of the pathogen-arthropod interface can be an important tool in control of these diseases.Ixodes ticks carry many pathogens of human importance, including Anaplasma, Babesia, Borrelia, tick-borne encephalitis virus and Powassan virus. The most researched of these pathogens is the spirochete Borrelia burgdorferi, the causative agent of Lyme disease and the most common vector-borne disease in the United States. [1][2][3] There are three important components to maintenance of the B. burgdorferi life cycle: the spirochete, the invertebrate tick vector and the vertebrate host (Figure 1).Ixodes ticks are haematophagous and take one blood meal during the larval, nymph and adult stage of their lifecycle. B. burgdorferi is not transmitted from adult ticks to eggs, so larval ticks must acquire the spirochetes from infected animals, such as birds and mice, with the first blood meal. The spirochetes will remain within the tick after feeding and moulting into the nymphal stage. A B. burgdorferi infected nymph will feed on another reservoir host and transmit the spirochetes, continuing the enzootic cycle. After another moult into the adult stage, the adult tick will typically feed on larger animals (such as deer) that may not be competent reservoir hosts for B. burgdorferi but are critical to tick mating. Ticks in the nymphal stage are primarily responsible for transmission of B. burgdorferi to humans, but humans are not important in the enzootic cycle and are considered dead-end hosts. 1The tick salivary glands and midgut play important roles in the colonization and transmission of B. burgdorferi. During acquisition from an infected host that occurs with the tick blood meal, B. burgdorferi enters the tick with blood and interacts with tick