Whereas selective amplification of B. burgdorferi RNA [69, 70] potentially may be able to circumvent potential sensitivity limitations in these approaches,

https://www.selleckchem.com/products/cbl0137-cbl-0137.html such amplification techniques may also incorporate inadvertent bias. Despite the caveats noted above, some key conclusions regarding activation of the RpoN-RpoS pathway can be drawn from our data. By comparing gene transcription data in ticks during acquisition (fed larvae, intermolt larvae), and in ticks during see more transmission (nymphal ticks during feeding), the RpoN-RpoS pathway is relatively quiescent in ticks during acquisition, but is initially activated and sustained in nymphs upon feeding. Similar to previous studies [17, 37], we assessed gene transcription by isolating RNA from whole ticks, which prevented temporal and spatial analyses of gene expression in specific tick

organs. In the future, by using dissected tick organs, gene expression in nymphal midguts and salivary glands at various times during tick feeding Selleckchem SB-715992 may be instructive for discerning how B. burgdorferi exploits the RpoN-RpoS pathway during its migration from midguts to salivary glands and subsequent entry into mammalian tissue. Some unknown factors from mammalian blood also may play critical roles in the induction of this regulatory pathway. Finally, our data demonstrate that the RpoN-RpoS pathway remains relatively active throughout the entire mammalian phase of infection. These combined findings provide further evidence for the central role of the RpoN-RpoS pathway, and its regulated genes, at the interface of B. burgdorferi transmission Tobramycin from tick to mammals and in the establishment of infection in animal hosts. Methods Bacterial strains and growth conditions Infectious, low passage (less than 3 passages) B. burgdorferi strain B31 was used throughout this study. B. burgdorferi was routinely cultured in either BSK-II medium or BSK-H medium (Sigma, St. Louis, MO) supplemented with 6% rabbit serum (Pel-Freeze, Rogers,

AR) [71]. Spirochetes were enumerated by dark-field microscopy. Infection of mice and ticks by B. burgdorferi All animal experiments were performed according to the protocols approved by the Institutional Animal Care and Use Committee (IACUC) at UT Southwestern Medical Center, Yale University, or the University of Maryland, College Park. To assess activation of the RpoN-RpoS pathway during mammalian infection, adult (4-6 weeks old) female C3H/HeN mice were purchased from Charles River laboratories (USA) and were infected with mid-logarithmic phase B. burgdorferi via intradermal needle injection (105 spirochetes per mouse) at the chest. Spirochetal infection was confirmed by PCR and culture [70].