burgdorferi could utilize chitin given that it is a major compone

burgdorferi could utilize chitin given that it is a major component of the tick peritrophic membrane [11–13]. Chitin utilization could prove beneficial to spirochetes

in the nutrient-limited environment of the unfed-infected tick midgut and aid in the colonization of the midgut epithelium. Prior to conducting growth studies in the presence of chitin, we determined if there was an inherent buy ABT-263 chitinase activity present in the medium. Previous reports characterized chitinase activity in goat serum [25], guinea pig blood [26], human JPH203 concentration macrophages [27] and a variety of mouse tissues [28]. While chitinase activity has not been previously described in rabbit serum, the evolutionary conservation of this enzymatic activity in rodents and primates [33] suggested that it may also be present in rabbit serum. We demonstrated heat-sensitive chitinase activity in rabbit serum (Table 1). In addition, rabbit serum showed no activity against 4-MUF GlcNAc, suggesting that it possesses chitinase activity but not a β-N-acetylglucosaminidase activity in which free GlcNAc is released from the non-reducing end of chitin. BIRB 796 price These results support our observation that the source of sequestered GlcNAc in the second exponential phase is not due to chito-oligomers present in the yeastolate component of BSK-II [17]. Any chito-oligomers present in yeastolate would be degraded to chitobiose by the chitinase activity present

in rabbit serum, and imported into the cells by the chbC transporter. To determine whether B. burgdorferi could utilize chitin and GlcNAc oligomers longer than chitobiose, we either inactivated the chitinase activity in rabbit serum by boiling before adding it to BSK-II or we replaced the rabbit

serum with a lipid extract. In both cases, B. burgdorferi cells provided with chitin or various chitin oligomers as the sole source of GlcNAc grew in one exponential phase to optimal cell densities (Figs. 1 and 3). In the absence of these added sources of GlcNAc, the cells failed to grow to high cell densities. These data strongly suggest that B. burgdorferi has the genes necessary to degrade and utilize chitin unless or GlcNAc oligomers in the absence of free GlcNAc. Additionally, GlcNAc starvation in the absence of rabbit serum resulted in biphasic growth, but with a lower maximum cell density in the second exponential phase (Fig. 3). This suggests that rabbit serum and one or more other components in BSK-II contribute the sequestered GlcNAc necessary for growth in the second exponential phase, possibly in the form of glycoproteins or glycosaminoglycans. It is interesting to note that boiling the serum or the entire medium had an impact on the ability of cells to grow in a second exponential phase in some experiments (Fig. 2B and Fig. 4). For example, in boiled medium without BSA, cells did not exhibit a second exponential phase in the absence of free GlcNAc (Fig. 2B).

Leave a Reply

Your email address will not be published. Required fields are marked *


You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>