Differential activation of human TLR4 by Escherichia coli and Shigella flexneri 2a lipopolysaccharide

Combined effects of lipid a acylation state and TLR4 polymorphisms on signaling

Prasad Rallabhandi, Agnes Awomoyi, Karen E. Thomas, Armelle Phalipon, Yukari Fujimoto, Koichi Fukase, Shoichi Kusumoto, Nilofer Qureshi, Marcelo B. Sztein, Stefanie N. Vogel

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

The lipid A of LPS activates TLR4 through an interaction with myeloid differentiation protein-2 (MD-2) and the degree of lipid A acylation affects TLR4 responsiveness. Two TLR4 single nucleotide polymorphisms (Asp 299Gly and Thr399Ile) have been associated with LPS hyporesponsiveness. We hypothesized that the combination of hypoacylation and these single nucleotide polymorphisms would exhibit a compounded effect on TLR4 signaling. HEK293T transfectants expressing wild-type or polymorphic TLR4 were stimulated with Escherichia coli (predominantly hexaacylated lipid A) or Shigella flexneri 2a (a mixture of hexaacylated, pentaacylated, and predominantly tetraacylated lipid A) LPS, or hexaacylated vs pentaacylated synthetic lipid As. NF-κB-reporter activity was significantly lower in response to S. flexneri 2a than E. coli LPS and further decreased in polymorphic transfectants. Neither hexaacylated nor pentaacylated synthetic lipid A induced NF-κB activity in wild-type transfectants under the identical transfection conditions used for LPS; however, increasing human MD-2 expression rescued responsiveness to hexaacylated lipid A only, while murine MD-2 was required to elicit a response to pentaacylated lipid A. Adherent PBMC of healthy volunteers were also compared for LPS-induced TNF-α, IL-6, IL-1β, and IL-10 production. Cytokine levels were significantly lower (∼20-90%) in response to S. flexneri than to E. coli LPS/lipid A and PBMC from polymorphic individuals secreted decreased cytokine levels in response to both LPS types and failed to respond to pentaacylated lipid A. Thus, the combination of acylation state and host genetics may significantly impact vaccine immunogenicity and/or efficacy, whether LPS is an integral component of a whole organism vaccine or included as an adjuvant.

Original languageEnglish
Pages (from-to)1139-1147
Number of pages9
JournalJournal of Immunology
Volume180
Issue number2
Publication statusPublished - 2008 Jan 15
Externally publishedYes

Fingerprint

Shigella flexneri
Lipid A
Acylation
Lipopolysaccharides
Escherichia coli
Lipids
Single Nucleotide Polymorphism
Cytokines
Viperidae
Interleukin-1
Interleukin-10
Transfection
Interleukin-6
Healthy Volunteers
Proteins
Vaccines

ASJC Scopus subject areas

  • Immunology

Cite this

Differential activation of human TLR4 by Escherichia coli and Shigella flexneri 2a lipopolysaccharide : Combined effects of lipid a acylation state and TLR4 polymorphisms on signaling. / Rallabhandi, Prasad; Awomoyi, Agnes; Thomas, Karen E.; Phalipon, Armelle; Fujimoto, Yukari; Fukase, Koichi; Kusumoto, Shoichi; Qureshi, Nilofer; Sztein, Marcelo B.; Vogel, Stefanie N.

In: Journal of Immunology, Vol. 180, No. 2, 15.01.2008, p. 1139-1147.

Research output: Contribution to journalArticle

Rallabhandi, P, Awomoyi, A, Thomas, KE, Phalipon, A, Fujimoto, Y, Fukase, K, Kusumoto, S, Qureshi, N, Sztein, MB & Vogel, SN 2008, 'Differential activation of human TLR4 by Escherichia coli and Shigella flexneri 2a lipopolysaccharide: Combined effects of lipid a acylation state and TLR4 polymorphisms on signaling', Journal of Immunology, vol. 180, no. 2, pp. 1139-1147.
Rallabhandi, Prasad ; Awomoyi, Agnes ; Thomas, Karen E. ; Phalipon, Armelle ; Fujimoto, Yukari ; Fukase, Koichi ; Kusumoto, Shoichi ; Qureshi, Nilofer ; Sztein, Marcelo B. ; Vogel, Stefanie N. / Differential activation of human TLR4 by Escherichia coli and Shigella flexneri 2a lipopolysaccharide : Combined effects of lipid a acylation state and TLR4 polymorphisms on signaling. In: Journal of Immunology. 2008 ; Vol. 180, No. 2. pp. 1139-1147.
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abstract = "The lipid A of LPS activates TLR4 through an interaction with myeloid differentiation protein-2 (MD-2) and the degree of lipid A acylation affects TLR4 responsiveness. Two TLR4 single nucleotide polymorphisms (Asp 299Gly and Thr399Ile) have been associated with LPS hyporesponsiveness. We hypothesized that the combination of hypoacylation and these single nucleotide polymorphisms would exhibit a compounded effect on TLR4 signaling. HEK293T transfectants expressing wild-type or polymorphic TLR4 were stimulated with Escherichia coli (predominantly hexaacylated lipid A) or Shigella flexneri 2a (a mixture of hexaacylated, pentaacylated, and predominantly tetraacylated lipid A) LPS, or hexaacylated vs pentaacylated synthetic lipid As. NF-κB-reporter activity was significantly lower in response to S. flexneri 2a than E. coli LPS and further decreased in polymorphic transfectants. Neither hexaacylated nor pentaacylated synthetic lipid A induced NF-κB activity in wild-type transfectants under the identical transfection conditions used for LPS; however, increasing human MD-2 expression rescued responsiveness to hexaacylated lipid A only, while murine MD-2 was required to elicit a response to pentaacylated lipid A. Adherent PBMC of healthy volunteers were also compared for LPS-induced TNF-α, IL-6, IL-1β, and IL-10 production. Cytokine levels were significantly lower (∼20-90{\%}) in response to S. flexneri than to E. coli LPS/lipid A and PBMC from polymorphic individuals secreted decreased cytokine levels in response to both LPS types and failed to respond to pentaacylated lipid A. Thus, the combination of acylation state and host genetics may significantly impact vaccine immunogenicity and/or efficacy, whether LPS is an integral component of a whole organism vaccine or included as an adjuvant.",
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