Abstract

BackgroundThe transport and catabolism of sialic acid, a critical virulence factor for nontypeable Haemophilus influenzae, is regulated by two transcription factors, SiaR and CRP.ResultsUsing a mutagenesis approach, glucosamine-6-phosphate (GlcN-6P) was identified as a co-activator for SiaR. Evidence for the cooperative regulation of both the sialic acid catabolic and transport operons suggested that cooperativity between SiaR and CRP is required for regulation. cAMP was unable to influence the expression of the catabolic operon in the absence of SiaR but was able to induce catabolic operon expression when both SiaR and GlcN-6P were present. Alteration of helical phasing supported this observation by uncoupling SiaR and CRP regulation. The insertion of one half-turn of DNA between the SiaR and CRP operators resulted in the loss of SiaR-mediated repression of the transport operon while eliminating cAMP-dependent induction of the catabolic operon when GlcN-6P was present. SiaR and CRP were found to bind to their respective operators simultaneously and GlcN-6P altered the interaction of SiaR with its operator.ConclusionsThese results suggest multiple novel features for the regulation of these two adjacent operons. SiaR functions as both a repressor and an activator and SiaR and CRP interact to regulate both operons from a single set of operators.

Highlights

  • The transport and catabolism of sialic acid, a critical virulence factor for nontypeable Haemophilus influenzae, is regulated by two transcription factors, SiaR and cAMP receptor protein (CRP)

  • The presence of sialic acid on the cell surface protects the cell from complement-mediated killing, the precise mechanism of this protection is unknown and may even vary among strains of nontypeable Haemophilus influenzae (NTHi) [3,4,5]

  • The putative CRP binding site is located at -59 to -80 relative to TS-1siaPT and at -59 to -80 relative to TS-1nan (Figure 2C)

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Summary

Introduction

The transport and catabolism of sialic acid, a critical virulence factor for nontypeable Haemophilus influenzae, is regulated by two transcription factors, SiaR and CRP. Sialic acid (5-N-acetylneuraminic acid, Neu5Ac) is used by nontypeable Haemophilus influenzae (NTHi) to assist in the evasion of the host innate immune response. The presence of sialic acid on the cell surface protects the cell from complement-mediated killing, the precise mechanism of this protection is unknown and may even vary among strains of NTHi [3,4,5]. NTHi possess a high-affinity transporter for sialic acid, encoded by siaPT

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