Lyme disease is caused by the spirochete and is transmitted via the bite of an infected tick. enters the skin， disseminates via the bloodstream， and infects various distal tissues， leading to inflammatory sequelae， such as Lyme arthritis and Lyme carditis. linear plasmid 36 (lp36) is critical for mammalian infectivity; however， the full complement of genes on lp36 that contribute to this process remains unknown. Through a targeted mutagenesis screen of the genes on lp36， we identified a novel infectivity gene of unknown function， ， which encodes an immunogenic， non-surface-exposed membrane protein that is important for efficient mammalian infection. Loss of resulted in reduced spirochete loads in distal tissues in a mouse model of infection. Through a detailed analysis of infection kinetics， we discovered that is important for promoting spirochete proliferation in the skin inoculation site. The attenuated ability of Δ spirochetes to proliferate in the inoculation site was followed by reduced numbers of spirochetes in the bloodstream and， ultimately， consistently reduced spirochete loads in distal tissues. Together， our data indicate that contributes to disseminated infection by promoting spirochete proliferation in the early phase of infection in the skin. This work not only increases the understanding of the contribution of the genes on lp36 to infection but also begins to define the genetic basis for expansion in the skin during localized infection and highlights the influence of the early expansion of spirochetes in the skin on the outcome of infection.