NAIP proteins are required for cytosolic detection of specific bacterial ligands in vivo
NLRs (nucleotide-binding domain [NBD] leucine-rich repeat [LRR]-containing proteins) exhibit diverse functions in innate and adaptive immunity. NAIPs (NLR family, apoptosis inhibitory proteins) are NLRs that appear to function as cytosolic immunoreceptors for specific bacterial proteins, including f...
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| Published in: | The Journal of experimental medicine Vol. 213; no. 5; p. 657 |
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| Main Authors: | , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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02.05.2016
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| ISSN: | 1540-9538, 1540-9538 |
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| Abstract | NLRs (nucleotide-binding domain [NBD] leucine-rich repeat [LRR]-containing proteins) exhibit diverse functions in innate and adaptive immunity. NAIPs (NLR family, apoptosis inhibitory proteins) are NLRs that appear to function as cytosolic immunoreceptors for specific bacterial proteins, including flagellin and the inner rod and needle proteins of bacterial type III secretion systems (T3SSs). Despite strong biochemical evidence implicating NAIPs in specific detection of bacterial ligands, genetic evidence has been lacking. Here we report the use of CRISPR/Cas9 to generate Naip1(-/-) and Naip2(-/-) mice, as well as Naip1-6(Δ/Δ) mice lacking all functional Naip genes. By challenging Naip1(-/-) or Naip2(-/-) mice with specific bacterial ligands in vivo, we demonstrate that Naip1 is uniquely required to detect T3SS needle protein and Naip2 is uniquely required to detect T3SS inner rod protein, but neither Naip1 nor Naip2 is required for detection of flagellin. Previously generated Naip5(-/-) mice retain some residual responsiveness to flagellin in vivo, whereas Naip1-6(Δ/Δ) mice fail to respond to cytosolic flagellin, consistent with previous biochemical data implicating NAIP6 in flagellin detection. Our results provide genetic evidence that specific NAIP proteins function to detect specific bacterial proteins in vivo. |
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| AbstractList | NLRs (nucleotide-binding domain [NBD] leucine-rich repeat [LRR]-containing proteins) exhibit diverse functions in innate and adaptive immunity. NAIPs (NLR family, apoptosis inhibitory proteins) are NLRs that appear to function as cytosolic immunoreceptors for specific bacterial proteins, including flagellin and the inner rod and needle proteins of bacterial type III secretion systems (T3SSs). Despite strong biochemical evidence implicating NAIPs in specific detection of bacterial ligands, genetic evidence has been lacking. Here we report the use of CRISPR/Cas9 to generate Naip1(-/-) and Naip2(-/-) mice, as well as Naip1-6(Δ/Δ) mice lacking all functional Naip genes. By challenging Naip1(-/-) or Naip2(-/-) mice with specific bacterial ligands in vivo, we demonstrate that Naip1 is uniquely required to detect T3SS needle protein and Naip2 is uniquely required to detect T3SS inner rod protein, but neither Naip1 nor Naip2 is required for detection of flagellin. Previously generated Naip5(-/-) mice retain some residual responsiveness to flagellin in vivo, whereas Naip1-6(Δ/Δ) mice fail to respond to cytosolic flagellin, consistent with previous biochemical data implicating NAIP6 in flagellin detection. Our results provide genetic evidence that specific NAIP proteins function to detect specific bacterial proteins in vivo. NLRs (nucleotide-binding domain [NBD] leucine-rich repeat [LRR]-containing proteins) exhibit diverse functions in innate and adaptive immunity. NAIPs (NLR family, apoptosis inhibitory proteins) are NLRs that appear to function as cytosolic immunoreceptors for specific bacterial proteins, including flagellin and the inner rod and needle proteins of bacterial type III secretion systems (T3SSs). Despite strong biochemical evidence implicating NAIPs in specific detection of bacterial ligands, genetic evidence has been lacking. Here we report the use of CRISPR/Cas9 to generate Naip1(-/-) and Naip2(-/-) mice, as well as Naip1-6(Δ/Δ) mice lacking all functional Naip genes. By challenging Naip1(-/-) or Naip2(-/-) mice with specific bacterial ligands in vivo, we demonstrate that Naip1 is uniquely required to detect T3SS needle protein and Naip2 is uniquely required to detect T3SS inner rod protein, but neither Naip1 nor Naip2 is required for detection of flagellin. Previously generated Naip5(-/-) mice retain some residual responsiveness to flagellin in vivo, whereas Naip1-6(Δ/Δ) mice fail to respond to cytosolic flagellin, consistent with previous biochemical data implicating NAIP6 in flagellin detection. Our results provide genetic evidence that specific NAIP proteins function to detect specific bacterial proteins in vivo.NLRs (nucleotide-binding domain [NBD] leucine-rich repeat [LRR]-containing proteins) exhibit diverse functions in innate and adaptive immunity. NAIPs (NLR family, apoptosis inhibitory proteins) are NLRs that appear to function as cytosolic immunoreceptors for specific bacterial proteins, including flagellin and the inner rod and needle proteins of bacterial type III secretion systems (T3SSs). Despite strong biochemical evidence implicating NAIPs in specific detection of bacterial ligands, genetic evidence has been lacking. Here we report the use of CRISPR/Cas9 to generate Naip1(-/-) and Naip2(-/-) mice, as well as Naip1-6(Δ/Δ) mice lacking all functional Naip genes. By challenging Naip1(-/-) or Naip2(-/-) mice with specific bacterial ligands in vivo, we demonstrate that Naip1 is uniquely required to detect T3SS needle protein and Naip2 is uniquely required to detect T3SS inner rod protein, but neither Naip1 nor Naip2 is required for detection of flagellin. Previously generated Naip5(-/-) mice retain some residual responsiveness to flagellin in vivo, whereas Naip1-6(Δ/Δ) mice fail to respond to cytosolic flagellin, consistent with previous biochemical data implicating NAIP6 in flagellin detection. Our results provide genetic evidence that specific NAIP proteins function to detect specific bacterial proteins in vivo. |
| Author | Kang, James J Nichols, Randilea D Kazmierczak, Barbara I Kang, Chulho Tenthorey, Jeannette L Vance, Russell E Rauch, Isabella Al Moussawi, Khatoun |
| Author_xml | – sequence: 1 givenname: Isabella surname: Rauch fullname: Rauch, Isabella organization: Division of Immunology and Pathogenesis, University of California, Berkeley, Berkeley, CA 94720 – sequence: 2 givenname: Jeannette L surname: Tenthorey fullname: Tenthorey, Jeannette L organization: Division of Immunology and Pathogenesis, University of California, Berkeley, Berkeley, CA 94720 – sequence: 3 givenname: Randilea D surname: Nichols fullname: Nichols, Randilea D organization: Division of Immunology and Pathogenesis, University of California, Berkeley, Berkeley, CA 94720 – sequence: 4 givenname: Khatoun surname: Al Moussawi fullname: Al Moussawi, Khatoun organization: Department of Medicine, Yale University School of Medicine, New Haven, CT 06510 – sequence: 5 givenname: James J surname: Kang fullname: Kang, James J organization: Division of Immunology and Pathogenesis, University of California, Berkeley, Berkeley, CA 94720 – sequence: 6 givenname: Chulho surname: Kang fullname: Kang, Chulho organization: Cancer Research Laboratory, University of California, Berkeley, Berkeley, CA 94720 – sequence: 7 givenname: Barbara I surname: Kazmierczak fullname: Kazmierczak, Barbara I organization: Department of Medicine, Yale University School of Medicine, New Haven, CT 06510 Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT 06510 – sequence: 8 givenname: Russell E surname: Vance fullname: Vance, Russell E email: rvance@berkeley.edu organization: Division of Immunology and Pathogenesis, University of California, Berkeley, Berkeley, CA 94720 Howard Hughes Medical Institute, University of California, Berkeley, Berkeley, CA 94720 Cancer Research Laboratory, University of California, Berkeley, Berkeley, CA 94720 rvance@berkeley.edu |
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| SubjectTerms | Animals Bacteria - genetics Bacteria - immunology Flagellin - genetics Flagellin - immunology Mice Mice, Knockout Neuronal Apoptosis-Inhibitory Protein - genetics Neuronal Apoptosis-Inhibitory Protein - immunology Type III Secretion Systems - genetics Type III Secretion Systems - immunology |
| Title | NAIP proteins are required for cytosolic detection of specific bacterial ligands in vivo |
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