Distinct Contributions of Neutrophils and CCR2 + Monocytes to Pulmonary Clearance of Different Klebsiella pneumoniae Strains
Klebsiella pneumoniae is a common respiratory pathogen, with some strains having developed broad resistance to clinically available antibiotics. Humans can become infected with many different K. pneumoniae strains that vary in genetic background, antibiotic susceptibility, capsule composition, and m...
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Published in | Infection and immunity Vol. 83; no. 9; pp. 3418 - 3427 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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United States
American Society for Microbiology
01.09.2015
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Abstract | Klebsiella pneumoniae
is a common respiratory pathogen, with some strains having developed broad resistance to clinically available antibiotics. Humans can become infected with many different
K. pneumoniae
strains that vary in genetic background, antibiotic susceptibility, capsule composition, and mucoid phenotype. Genome comparisons have revealed differences between
K. pneumoniae
strains, but the impact of genomic variability on immune-mediated clearance of pneumonia remains unclear. Experimental studies of pneumonia in mice have used the rodent-adapted 43816 strain of
K. pneumoniae
and demonstrated that neutrophils are essential for optimal host defense. It remains unclear, however, whether CCR2
+
monocytes contribute to
K. pneumoniae
clearance from the lung. We selectively depleted neutrophils, CCR2
+
monocytes, or both from immunocompetent mice and determined susceptibility to infection by the 43816 strain and 4 newly isolated clinical
K. pneumoniae
strains. The clinical
K. pneumoniae
strains, including one carbapenem-resistant ST258 strain, are less virulent than 43816. Optimal clearance of each of the 5 strains required either neutrophils or CCR2
+
monocytes. Selective neutrophil depletion markedly worsened infection with
K. pneumoniae
strain 43816 and three clinical isolates but did not increase susceptibility of mice to infection with the carbapenem-resistant
K. pneumoniae
ST258 strain. Depletion of CCR2
+
monocytes delayed recovery from infection with each of the 5
K. pneumoniae
strains, revealing a contribution of these cells to bacterial clearance from the lung. Our findings demonstrate strain-dependent variation in the contributions of neutrophils and CCR2
+
monocytes to clearance of
K. pneumoniae
pulmonary infection. |
---|---|
AbstractList | Klebsiella pneumoniae is a common respiratory pathogen, with some strains having developed broad resistance to clinically available antibiotics. Humans can become infected with many different K. pneumoniae strains that vary in genetic background, antibiotic susceptibility, capsule composition, and mucoid phenotype. Genome comparisons have revealed differences between K. pneumoniae strains, but the impact of genomic variability on immune-mediated clearance of pneumonia remains unclear. Experimental studies of pneumonia in mice have used the rodent-adapted 43816 strain of K. pneumoniae and demonstrated that neutrophils are essential for optimal host defense. It remains unclear, however, whether CCR2(+) monocytes contribute to K. pneumoniae clearance from the lung. We selectively depleted neutrophils, CCR2(+) monocytes, or both from immunocompetent mice and determined susceptibility to infection by the 43816 strain and 4 newly isolated clinical K. pneumoniae strains. The clinical K. pneumoniae strains, including one carbapenem-resistant ST258 strain, are less virulent than 43816. Optimal clearance of each of the 5 strains required either neutrophils or CCR2(+) monocytes. Selective neutrophil depletion markedly worsened infection with K. pneumoniae strain 43816 and three clinical isolates but did not increase susceptibility of mice to infection with the carbapenem-resistant K. pneumoniae ST258 strain. Depletion of CCR2(+) monocytes delayed recovery from infection with each of the 5 K. pneumoniae strains, revealing a contribution of these cells to bacterial clearance from the lung. Our findings demonstrate strain-dependent variation in the contributions of neutrophils and CCR2(+) monocytes to clearance of K. pneumoniae pulmonary infection.Klebsiella pneumoniae is a common respiratory pathogen, with some strains having developed broad resistance to clinically available antibiotics. Humans can become infected with many different K. pneumoniae strains that vary in genetic background, antibiotic susceptibility, capsule composition, and mucoid phenotype. Genome comparisons have revealed differences between K. pneumoniae strains, but the impact of genomic variability on immune-mediated clearance of pneumonia remains unclear. Experimental studies of pneumonia in mice have used the rodent-adapted 43816 strain of K. pneumoniae and demonstrated that neutrophils are essential for optimal host defense. It remains unclear, however, whether CCR2(+) monocytes contribute to K. pneumoniae clearance from the lung. We selectively depleted neutrophils, CCR2(+) monocytes, or both from immunocompetent mice and determined susceptibility to infection by the 43816 strain and 4 newly isolated clinical K. pneumoniae strains. The clinical K. pneumoniae strains, including one carbapenem-resistant ST258 strain, are less virulent than 43816. Optimal clearance of each of the 5 strains required either neutrophils or CCR2(+) monocytes. Selective neutrophil depletion markedly worsened infection with K. pneumoniae strain 43816 and three clinical isolates but did not increase susceptibility of mice to infection with the carbapenem-resistant K. pneumoniae ST258 strain. Depletion of CCR2(+) monocytes delayed recovery from infection with each of the 5 K. pneumoniae strains, revealing a contribution of these cells to bacterial clearance from the lung. Our findings demonstrate strain-dependent variation in the contributions of neutrophils and CCR2(+) monocytes to clearance of K. pneumoniae pulmonary infection. Klebsiella pneumoniae is a common respiratory pathogen, with some strains having developed broad resistance to clinically available antibiotics. Humans can become infected with many different K. pneumoniae strains that vary in genetic background, antibiotic susceptibility, capsule composition, and mucoid phenotype. Genome comparisons have revealed differences between K. pneumoniae strains, but the impact of genomic variability on immune-mediated clearance of pneumonia remains unclear. Experimental studies of pneumonia in mice have used the rodent-adapted 43816 strain of K. pneumoniae and demonstrated that neutrophils are essential for optimal host defense. It remains unclear, however, whether CCR2 + monocytes contribute to K. pneumoniae clearance from the lung. We selectively depleted neutrophils, CCR2 + monocytes, or both from immunocompetent mice and determined susceptibility to infection by the 43816 strain and 4 newly isolated clinical K. pneumoniae strains. The clinical K. pneumoniae strains, including one carbapenem-resistant ST258 strain, are less virulent than 43816. Optimal clearance of each of the 5 strains required either neutrophils or CCR2 + monocytes. Selective neutrophil depletion markedly worsened infection with K. pneumoniae strain 43816 and three clinical isolates but did not increase susceptibility of mice to infection with the carbapenem-resistant K. pneumoniae ST258 strain. Depletion of CCR2 + monocytes delayed recovery from infection with each of the 5 K. pneumoniae strains, revealing a contribution of these cells to bacterial clearance from the lung. Our findings demonstrate strain-dependent variation in the contributions of neutrophils and CCR2 + monocytes to clearance of K. pneumoniae pulmonary infection. Klebsiella pneumoniae is a common respiratory pathogen, with some strains having developed broad resistance to clinically available antibiotics. Humans can become infected with many different K. pneumoniae strains that vary in genetic background, antibiotic susceptibility, capsule composition, and mucoid phenotype. Genome comparisons have revealed differences between K. pneumoniae strains, but the impact of genomic variability on immune-mediated clearance of pneumonia remains unclear. Experimental studies of pneumonia in mice have used the rodent-adapted 43816 strain of K. pneumoniae and demonstrated that neutrophils are essential for optimal host defense. It remains unclear, however, whether CCR2(+) monocytes contribute to K. pneumoniae clearance from the lung. We selectively depleted neutrophils, CCR2(+) monocytes, or both from immunocompetent mice and determined susceptibility to infection by the 43816 strain and 4 newly isolated clinical K. pneumoniae strains. The clinical K. pneumoniae strains, including one carbapenem-resistant ST258 strain, are less virulent than 43816. Optimal clearance of each of the 5 strains required either neutrophils or CCR2(+) monocytes. Selective neutrophil depletion markedly worsened infection with K. pneumoniae strain 43816 and three clinical isolates but did not increase susceptibility of mice to infection with the carbapenem-resistant K. pneumoniae ST258 strain. Depletion of CCR2(+) monocytes delayed recovery from infection with each of the 5 K. pneumoniae strains, revealing a contribution of these cells to bacterial clearance from the lung. Our findings demonstrate strain-dependent variation in the contributions of neutrophils and CCR2(+) monocytes to clearance of K. pneumoniae pulmonary infection. |
Author | Carter, Rebecca A. Leiner, Ingrid M. Xiong, Huizhong Chen, Liang Kreiswirth, Barry N. Pamer, Eric G. Tang, Yi-Wei |
Author_xml | – sequence: 1 givenname: Huizhong surname: Xiong fullname: Xiong, Huizhong organization: Immunology Program, Sloan Kettering Institute, New York, New York, USA, Infectious Diseases Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA – sequence: 2 givenname: Rebecca A. surname: Carter fullname: Carter, Rebecca A. organization: Immunology Program, Sloan Kettering Institute, New York, New York, USA, Infectious Diseases Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA – sequence: 3 givenname: Ingrid M. surname: Leiner fullname: Leiner, Ingrid M. organization: Immunology Program, Sloan Kettering Institute, New York, New York, USA, Infectious Diseases Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA – sequence: 4 givenname: Yi-Wei surname: Tang fullname: Tang, Yi-Wei organization: Infectious Diseases Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA, Clinical Microbiology Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA – sequence: 5 givenname: Liang surname: Chen fullname: Chen, Liang organization: Public Health Research Institute Center, New Jersey Medical School—Rutgers, The State University of New Jersey, Newark, New Jersey, USA – sequence: 6 givenname: Barry N. surname: Kreiswirth fullname: Kreiswirth, Barry N. organization: Public Health Research Institute Center, New Jersey Medical School—Rutgers, The State University of New Jersey, Newark, New Jersey, USA – sequence: 7 givenname: Eric G. surname: Pamer fullname: Pamer, Eric G. organization: Immunology Program, Sloan Kettering Institute, New York, New York, USA, Infectious Diseases Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA, Clinical Microbiology Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA |
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Cites_doi | 10.1093/infdis/jit820 10.1016/j.imbio.2014.08.007 10.1172/JCI41649 10.1128/IAI.69.4.2017-2024.2001 10.1056/NEJMp1011715 10.1128/IAI.73.1.532-545.2005 10.7554/eLife.01086 10.1111/j.1365-2958.2005.04918.x 10.1371/journal.pone.0020333 10.1038/nm1710 10.4049/jimmunol.0903843 10.4049/jimmunol.155.2.722 10.1189/jlb.1212622 10.1016/j.immuni.2011.02.016 10.1084/jem.194.4.519 10.1152/ajplung.00194.2013 10.4049/jimmunol.177.1.538 10.4049/jimmunol.1101985 10.1128/JCM.01924-13 10.12703/P6-80 10.1016/j.chom.2009.10.007 10.1086/430126 10.1371/journal.ppat.1003940 10.1016/S1074-7613(03)00263-2 10.1128/JCM.43.8.4178-4182.2005 10.4049/jimmunol.1101721 10.1016/j.ijantimicag.2007.06.019 10.4049/jimmunol.0901033 10.1038/nri3070 10.1097/QCO.0b013e3283630dd3 10.1172/JCI27009 10.1016/S1473-3099(12)70205-0 10.1016/j.tim.2014.09.003 10.4049/jimmunol.161.5.2435 10.1097/MCP.0b013e328351f974 10.1128/iai.64.12.5211-5218.1996 10.1056/NEJMra0904124 10.1093/infdis/jiu157 10.1016/S1074-7613(03)00171-7 10.1093/infdis/jis673 10.4049/jimmunol.1200195 10.1152/ajplung.00415.2010 10.1038/ni1261 |
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Copyright | Copyright © 2015, American Society for Microbiology. All Rights Reserved. Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Citation Xiong H, Carter RA, Leiner IM, Tang Y-W, Chen L, Kreiswirth BN, Pamer EG. 2015. Distinct contributions of neutrophils and CCR2+ monocytes to pulmonary clearance of different Klebsiella pneumoniae strains. Infect Immun 83:3418–3427. doi:10.1128/IAI.00678-15. |
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References | Greenberger MJ (e_1_3_3_31_2) 1995; 155 e_1_3_3_17_2 e_1_3_3_16_2 e_1_3_3_19_2 e_1_3_3_38_2 e_1_3_3_18_2 e_1_3_3_39_2 e_1_3_3_13_2 e_1_3_3_36_2 e_1_3_3_12_2 e_1_3_3_37_2 e_1_3_3_15_2 e_1_3_3_34_2 e_1_3_3_14_2 e_1_3_3_35_2 e_1_3_3_32_2 e_1_3_3_33_2 e_1_3_3_11_2 Patel JB (e_1_3_3_25_2) 2014 e_1_3_3_30_2 e_1_3_3_10_2 e_1_3_3_40_2 e_1_3_3_6_2 e_1_3_3_5_2 e_1_3_3_8_2 e_1_3_3_7_2 e_1_3_3_28_2 e_1_3_3_27_2 e_1_3_3_29_2 e_1_3_3_24_2 e_1_3_3_23_2 e_1_3_3_26_2 e_1_3_3_45_2 e_1_3_3_2_2 Tsai WC (e_1_3_3_9_2) 1998; 161 e_1_3_3_20_2 e_1_3_3_43_2 e_1_3_3_44_2 e_1_3_3_4_2 e_1_3_3_22_2 e_1_3_3_41_2 e_1_3_3_3_2 e_1_3_3_21_2 e_1_3_3_42_2 21458307 - Immunity. 2011 Apr 22;34(4):590-601 23806896 - Curr Opin Infect Dis. 2013 Aug;26(4):332-7 25343037 - F1000Prime Rep. 2014 Sep 04;6:80 21158655 - N Engl J Med. 2010 Dec 16;363(25):2377-9 24353272 - J Infect Dis. 2014 Jun 1;209(11):1837-46 21647421 - PLoS One. 2011;6(5):e20333 25304194 - Trends Microbiol. 2014 Dec;22(12):686-96 14563322 - Immunity. 2003 Oct;19(4):583-93 23125447 - J Infect Dis. 2013 Jan 15;207(2):331-9 24586155 - PLoS Pathog. 2014 Feb;10(2):e1003940 15983903 - Clin Infect Dis. 2005 Aug 1;41 Suppl 3:S213-7 11254553 - Infect Immun. 2001 Apr;69(4):2017-24 9725241 - J Immunol. 1998 Sep 1;161(5):2435-40 18264110 - Nat Med. 2008 Mar;14(3):275-81 19846873 - J Immunol. 2009 Nov 15;183(10):6629-38 16485040 - J Clin Invest. 2006 Mar;116(3):695-702 20937845 - J Immunol. 2010 Nov 15;185(10):6214-25 21976773 - J Immunol. 2011 Nov 15;187(10):5293-8 24220507 - Elife. 2013;2:e01086 16081970 - J Clin Microbiol. 2005 Aug;43(8):4178-82 22160309 - Am J Physiol Lung Cell Mol Physiol. 2012 Mar 1;302(5):L447-54 16262790 - Mol Microbiol. 2005 Nov;58(4):1054-73 22379035 - J Immunol. 2012 Apr 1;188(7):3458-68 24634498 - J Infect Dis. 2014 Sep 1;210(5):803-13 8945568 - Infect Immun. 1996 Dec;64(12):5211-8 16200068 - Nat Immunol. 2005 Nov;6(11):1133-41 12871639 - Immunity. 2003 Jul;19(1):59-70 15618193 - Infect Immun. 2005 Jan;73(1):532-45 17716872 - Int J Antimicrob Agents. 2007 Nov;30(5):385-9 25214476 - Immunobiology. 2015 Feb;220(2):210-4 23709686 - J Leukoc Biol. 2013 Sep;94(3):393-8 24056971 - Am J Physiol Lung Cell Mol Physiol. 2013 Nov 15;305(10):L702-11 19917501 - Cell Host Microbe. 2009 Nov 19;6(5):470-81 20463340 - N Engl J Med. 2010 May 13;362(19):1804-13 23099082 - Lancet Infect Dis. 2012 Nov;12(11):881-7 21984070 - Nat Rev Immunol. 2011 Nov;11(11):762-74 22547706 - J Immunol. 2012 Jun 1;188(11):5623-35 7608550 - J Immunol. 1995 Jul 15;155(2):722-9 11514607 - J Exp Med. 2001 Aug 20;194(4):519-27 20516641 - J Clin Invest. 2010 Jul;120(7):2423-31 24088853 - J Clin Microbiol. 2013 Dec;51(12):4073-8 22366995 - Curr Opin Pulm Med. 2012 May;18(3):187-93 16785551 - J Immunol. 2006 Jul 1;177(1):538-47 |
References_xml | – ident: e_1_3_3_13_2 doi: 10.1093/infdis/jit820 – ident: e_1_3_3_41_2 doi: 10.1016/j.imbio.2014.08.007 – ident: e_1_3_3_43_2 doi: 10.1172/JCI41649 – ident: e_1_3_3_45_2 doi: 10.1128/IAI.69.4.2017-2024.2001 – ident: e_1_3_3_3_2 doi: 10.1056/NEJMp1011715 – ident: e_1_3_3_29_2 doi: 10.1128/IAI.73.1.532-545.2005 – ident: e_1_3_3_40_2 doi: 10.7554/eLife.01086 – ident: e_1_3_3_32_2 doi: 10.1111/j.1365-2958.2005.04918.x – ident: e_1_3_3_37_2 doi: 10.1371/journal.pone.0020333 – ident: e_1_3_3_36_2 doi: 10.1038/nm1710 – ident: e_1_3_3_8_2 doi: 10.4049/jimmunol.0903843 – volume: 155 start-page: 722 year: 1995 ident: e_1_3_3_31_2 article-title: Neutralization of IL-10 increases survival in a murine model of Klebsiella pneumonia publication-title: J Immunol doi: 10.4049/jimmunol.155.2.722 – ident: e_1_3_3_14_2 doi: 10.1189/jlb.1212622 – ident: e_1_3_3_21_2 doi: 10.1016/j.immuni.2011.02.016 – ident: e_1_3_3_15_2 doi: 10.1084/jem.194.4.519 – ident: e_1_3_3_23_2 doi: 10.1152/ajplung.00194.2013 – volume-title: CLSI document M100-S24 34 year: 2014 ident: e_1_3_3_25_2 – ident: e_1_3_3_5_2 doi: 10.4049/jimmunol.177.1.538 – ident: e_1_3_3_7_2 doi: 10.4049/jimmunol.1101985 – ident: e_1_3_3_27_2 doi: 10.1128/JCM.01924-13 – ident: e_1_3_3_4_2 doi: 10.12703/P6-80 – ident: e_1_3_3_24_2 doi: 10.1016/j.chom.2009.10.007 – ident: e_1_3_3_34_2 doi: 10.1086/430126 – ident: e_1_3_3_39_2 doi: 10.1371/journal.ppat.1003940 – ident: e_1_3_3_44_2 doi: 10.1016/S1074-7613(03)00263-2 – ident: e_1_3_3_26_2 doi: 10.1128/JCM.43.8.4178-4182.2005 – ident: e_1_3_3_35_2 doi: 10.4049/jimmunol.1101721 – ident: e_1_3_3_17_2 doi: 10.1016/j.ijantimicag.2007.06.019 – ident: e_1_3_3_10_2 doi: 10.4049/jimmunol.0901033 – ident: e_1_3_3_30_2 doi: 10.1038/nri3070 – ident: e_1_3_3_16_2 doi: 10.1097/QCO.0b013e3283630dd3 – ident: e_1_3_3_42_2 doi: 10.1172/JCI27009 – ident: e_1_3_3_19_2 doi: 10.1016/S1473-3099(12)70205-0 – ident: e_1_3_3_28_2 doi: 10.1016/j.tim.2014.09.003 – volume: 161 start-page: 2435 year: 1998 ident: e_1_3_3_9_2 article-title: Lung-specific transgenic expression of KC enhances resistance to Klebsiella pneumoniae in mice publication-title: J Immunol doi: 10.4049/jimmunol.161.5.2435 – ident: e_1_3_3_18_2 doi: 10.1097/MCP.0b013e328351f974 – ident: e_1_3_3_33_2 doi: 10.1128/iai.64.12.5211-5218.1996 – ident: e_1_3_3_2_2 doi: 10.1056/NEJMra0904124 – ident: e_1_3_3_20_2 doi: 10.1093/infdis/jiu157 – ident: e_1_3_3_22_2 doi: 10.1016/S1074-7613(03)00171-7 – ident: e_1_3_3_6_2 doi: 10.1093/infdis/jis673 – ident: e_1_3_3_11_2 doi: 10.4049/jimmunol.1200195 – ident: e_1_3_3_12_2 doi: 10.1152/ajplung.00415.2010 – ident: e_1_3_3_38_2 doi: 10.1038/ni1261 – reference: 8945568 - Infect Immun. 1996 Dec;64(12):5211-8 – reference: 21458307 - Immunity. 2011 Apr 22;34(4):590-601 – reference: 19917501 - Cell Host Microbe. 2009 Nov 19;6(5):470-81 – reference: 20516641 - J Clin Invest. 2010 Jul;120(7):2423-31 – reference: 22547706 - J Immunol. 2012 Jun 1;188(11):5623-35 – reference: 22379035 - J Immunol. 2012 Apr 1;188(7):3458-68 – reference: 25304194 - Trends Microbiol. 2014 Dec;22(12):686-96 – reference: 25214476 - Immunobiology. 2015 Feb;220(2):210-4 – reference: 24634498 - J Infect Dis. 2014 Sep 1;210(5):803-13 – reference: 24088853 - J Clin Microbiol. 2013 Dec;51(12):4073-8 – reference: 7608550 - J Immunol. 1995 Jul 15;155(2):722-9 – reference: 9725241 - J Immunol. 1998 Sep 1;161(5):2435-40 – reference: 24220507 - Elife. 2013;2:e01086 – reference: 22160309 - Am J Physiol Lung Cell Mol Physiol. 2012 Mar 1;302(5):L447-54 – reference: 23709686 - J Leukoc Biol. 2013 Sep;94(3):393-8 – reference: 11514607 - J Exp Med. 2001 Aug 20;194(4):519-27 – reference: 18264110 - Nat Med. 2008 Mar;14(3):275-81 – reference: 16200068 - Nat Immunol. 2005 Nov;6(11):1133-41 – reference: 24056971 - Am J Physiol Lung Cell Mol Physiol. 2013 Nov 15;305(10):L702-11 – reference: 21647421 - PLoS One. 2011;6(5):e20333 – reference: 24586155 - PLoS Pathog. 2014 Feb;10(2):e1003940 – reference: 22366995 - Curr Opin Pulm Med. 2012 May;18(3):187-93 – reference: 16262790 - Mol Microbiol. 2005 Nov;58(4):1054-73 – reference: 11254553 - Infect Immun. 2001 Apr;69(4):2017-24 – reference: 23806896 - Curr Opin Infect Dis. 2013 Aug;26(4):332-7 – reference: 23099082 - Lancet Infect Dis. 2012 Nov;12(11):881-7 – reference: 23125447 - J Infect Dis. 2013 Jan 15;207(2):331-9 – reference: 19846873 - J Immunol. 2009 Nov 15;183(10):6629-38 – reference: 15983903 - Clin Infect Dis. 2005 Aug 1;41 Suppl 3:S213-7 – reference: 21158655 - N Engl J Med. 2010 Dec 16;363(25):2377-9 – reference: 16785551 - J Immunol. 2006 Jul 1;177(1):538-47 – reference: 20937845 - J Immunol. 2010 Nov 15;185(10):6214-25 – reference: 15618193 - Infect Immun. 2005 Jan;73(1):532-45 – reference: 21984070 - Nat Rev Immunol. 2011 Nov;11(11):762-74 – reference: 17716872 - Int J Antimicrob Agents. 2007 Nov;30(5):385-9 – reference: 24353272 - J Infect Dis. 2014 Jun 1;209(11):1837-46 – reference: 21976773 - J Immunol. 2011 Nov 15;187(10):5293-8 – reference: 12871639 - Immunity. 2003 Jul;19(1):59-70 – reference: 20463340 - N Engl J Med. 2010 May 13;362(19):1804-13 – reference: 25343037 - F1000Prime Rep. 2014 Sep 04;6:80 – reference: 16081970 - J Clin Microbiol. 2005 Aug;43(8):4178-82 – reference: 14563322 - Immunity. 2003 Oct;19(4):583-93 – reference: 16485040 - J Clin Invest. 2006 Mar;116(3):695-702 |
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Snippet | Klebsiella pneumoniae
is a common respiratory pathogen, with some strains having developed broad resistance to clinically available antibiotics. Humans can... Klebsiella pneumoniae is a common respiratory pathogen, with some strains having developed broad resistance to clinically available antibiotics. Humans can... |
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SubjectTerms | Animals Bacterial Infections Disease Models, Animal Klebsiella Infections - immunology Klebsiella Infections - microbiology Klebsiella pneumoniae - immunology Mice Mice, Inbred C57BL Monocytes - immunology Neutrophils - immunology Receptors, CCR2 - immunology Respiratory Tract Infections - immunology Respiratory Tract Infections - microbiology |
Title | Distinct Contributions of Neutrophils and CCR2 + Monocytes to Pulmonary Clearance of Different Klebsiella pneumoniae Strains |
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