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...

Full description

Saved in:
Bibliographic Details
Published inInfection and immunity Vol. 83; no. 9; pp. 3418 - 3427
Main Authors Xiong, Huizhong, Carter, Rebecca A., Leiner, Ingrid M., Tang, Yi-Wei, Chen, Liang, Kreiswirth, Barry N., Pamer, Eric G.
Format Journal Article
LanguageEnglish
Published United States American Society for Microbiology 01.09.2015
Subjects
Online AccessGet full text

Cover

Loading…
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
BackLink https://www.ncbi.nlm.nih.gov/pubmed/26056382$$D View this record in MEDLINE/PubMed
BookMark eNptkdtrFTEQxoNU7Gn1zWfJo6DbJtlkT_IilK2XQ-sFL88hm53YSE5ymmSFQv94d20tVnwahvnNN5fvAO3FFAGhp5QcUcrk8eZkc0RIt5YNFQ_QihIlGyEY20MrQqhqlOjW--iglB9zyjmXj9A-64joWslW6PrUl-qjrbhPsWY_TNWnWHBy-ANMNafdhQ8Fmzjivv_M8Av8PsVkryoUXBP-NIVtiiZf4T6AySZaWFpPvXOQIVZ8FmAoHkIweBdhmmFvAH-p2fhYHqOHzoQCT27jIfr25vXX_l1z_vHtpj85bywXpDaKDcR1o1JGsDV01jABAxNsvsCKVgknOeVkJHYYgHAJHbGSjsoMgjknQbaH6NWN7m4atjDaebFsgt5lv51X18l4fb8S_YX-nn5qLlreiUXg-a1ATpcTlKq3vtjlqghpKpquCW-5bNWCPvt71t2QPy-fgZc3gM2plAzuDqFEL47q2VH921FNxYyzf3Drq1lMWn4Y_t_0C69bpbM
CitedBy_id crossref_primary_10_3389_fcimb_2022_1050396
crossref_primary_10_1016_j_cell_2016_03_017
crossref_primary_10_1002_JLB_4HI0519_155R
crossref_primary_10_1002_path_5601
crossref_primary_10_1093_infdis_jiw378
crossref_primary_10_1172_jci_insight_150239
crossref_primary_10_1002_JLB_MR0618_233R
crossref_primary_10_1038_s41392_023_01490_9
crossref_primary_10_1093_infdis_jiw405
crossref_primary_10_3390_cancers12113376
crossref_primary_10_1093_femsre_fuy043
crossref_primary_10_3390_microorganisms8050735
crossref_primary_10_1172_JCI124615
crossref_primary_10_1371_journal_ppat_1010693
crossref_primary_10_21307_pjm_2018_033
crossref_primary_10_1016_j_micinf_2024_105369
crossref_primary_10_3390_pathogens11091063
crossref_primary_10_1128_IAI_00665_18
crossref_primary_10_1172_jci_insight_89704
crossref_primary_10_3390_ijms23116246
crossref_primary_10_3390_ijms23137361
crossref_primary_10_1161_ATVBAHA_118_311332
crossref_primary_10_3389_fimmu_2022_826047
crossref_primary_10_1038_s41579_024_01105_2
crossref_primary_10_1097_IN9_0000000000000028
crossref_primary_10_1177_1753425920942582
crossref_primary_10_4049_jimmunol_1600306
crossref_primary_10_1084_jem_20212032
crossref_primary_10_3390_microorganisms12112197
crossref_primary_10_1016_j_tim_2025_01_003
crossref_primary_10_1126_sciadv_adl6162
crossref_primary_10_1128_mBio_01443_18
crossref_primary_10_1128_mBio_02663_18
crossref_primary_10_1371_journal_ppat_1006748
crossref_primary_10_1128_mBio_02059_20
crossref_primary_10_1128_mbio_03792_21
crossref_primary_10_1084_jem_20181639
crossref_primary_10_3389_fcimb_2022_934671
crossref_primary_10_1155_2021_6646071
crossref_primary_10_3389_fmicb_2018_02047
crossref_primary_10_3390_ijms25010309
crossref_primary_10_1038_s41590_018_0293_x
crossref_primary_10_1038_s41467_025_56095_3
crossref_primary_10_1016_j_cellimm_2024_104841
crossref_primary_10_1016_j_smim_2016_03_014
crossref_primary_10_7554_eLife_56656
crossref_primary_10_1152_physrev_00032_2017
crossref_primary_10_3389_fcimb_2020_571771
crossref_primary_10_1111_jth_13408
crossref_primary_10_1186_s13568_022_01465_z
crossref_primary_10_1128_mBio_02802_19
crossref_primary_10_1099_acmi_0_000275
crossref_primary_10_1177_0271678X20909055
crossref_primary_10_3389_fimmu_2024_1450486
crossref_primary_10_1186_s41479_023_00106_8
crossref_primary_10_3389_fimmu_2019_00929
crossref_primary_10_1038_s41467_024_47149_z
crossref_primary_10_1371_journal_ppat_1011233
crossref_primary_10_1038_s41598_021_00211_y
crossref_primary_10_1080_19490976_2024_2340486
crossref_primary_10_1186_s40635_020_00336_w
crossref_primary_10_1128_AAC_02674_18
crossref_primary_10_1152_ajplung_00422_2019
crossref_primary_10_1371_journal_pone_0170125
crossref_primary_10_1371_journal_ppat_1011900
crossref_primary_10_1093_femspd_ftab009
crossref_primary_10_1186_s40635_021_00398_4
crossref_primary_10_1371_journal_ppat_1009309
crossref_primary_10_1038_s41385_020_0300_z
crossref_primary_10_1159_000487515
crossref_primary_10_1128_spectrum_01760_22
crossref_primary_10_1186_s12974_024_03093_9
crossref_primary_10_1155_2022_5336931
crossref_primary_10_1016_j_xcrm_2024_101886
crossref_primary_10_1128_iai_00012_24
crossref_primary_10_1016_j_celrep_2021_109196
crossref_primary_10_1128_iai_00224_22
crossref_primary_10_1128_IAI_00362_19
crossref_primary_10_1038_s41572_021_00259_0
crossref_primary_10_1128_IAI_00693_20
crossref_primary_10_1128_mbio_03838_24
crossref_primary_10_1126_scitranslmed_ade0054
crossref_primary_10_1371_journal_ppat_1006309
crossref_primary_10_1016_j_ejphar_2017_08_002
crossref_primary_10_1159_000518679
crossref_primary_10_1128_MMBR_00078_15
crossref_primary_10_1128_IAI_00135_18
crossref_primary_10_22141_2224_0551_16_1_2021_226459
crossref_primary_10_15252_emmm_202216888
crossref_primary_10_1038_cmi_2016_69
crossref_primary_10_1099_jmm_0_001222
crossref_primary_10_1172_jci_insight_92774
crossref_primary_10_1128_aac_01429_23
crossref_primary_10_1016_j_celrep_2022_111167
crossref_primary_10_1038_s41467_022_31990_1
crossref_primary_10_1152_ajplung_00008_2021
crossref_primary_10_1038_s41385_018_0106_4
crossref_primary_10_1186_s12879_022_07558_1
crossref_primary_10_1016_j_isci_2021_102871
crossref_primary_10_4251_wjgo_v13_i12_2013
crossref_primary_10_1016_j_mib_2020_01_006
crossref_primary_10_1371_journal_pone_0188251
crossref_primary_10_1073_pnas_1607787113
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
ContentType Journal Article
Copyright Copyright © 2015, American Society for Microbiology. All Rights Reserved.
Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology
Copyright_xml – notice: Copyright © 2015, American Society for Microbiology. All Rights Reserved.
– notice: Copyright © 2015, American Society for Microbiology. All Rights Reserved. 2015 American Society for Microbiology
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
DOI 10.1128/IAI.00678-15
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

MEDLINE
CrossRef
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Biology
DocumentTitleAlternate Monocyte-Mediated Defense against K. pneumoniae
EISSN 1098-5522
EndPage 3427
ExternalDocumentID PMC4534658
26056382
10_1128_IAI_00678_15
Genre Journal Article
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: PHS HHS
  grantid: A023766
– fundername: NCI NIH HHS
  grantid: P01 CA023766
– fundername: NIAID NIH HHS
  grantid: R01 AI090155
– fundername: NIAID NIH HHS
  grantid: R37AI039031
– fundername: NIAID NIH HHS
  grantid: R37 AI039031
– fundername: NCI NIH HHS
  grantid: P30 CA008748
– fundername: NIAID NIH HHS
  grantid: R01AI090155
GroupedDBID ---
-DZ
-~X
.55
.GJ
0R~
18M
29I
2WC
39C
3O-
4.4
41~
53G
5GY
5RE
5VS
85S
AAGFI
AAYXX
ABOCM
ACGFO
ADBBV
ADXHL
AENEX
AGCDD
AGVNZ
AI.
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BAWUL
BTFSW
C1A
CITATION
CS3
D0S
DIK
DU5
E3Z
EBS
EJD
F5P
FRP
GX1
H13
HYE
HZ~
H~9
IH2
J5H
KQ8
L7B
MVM
NEJ
O9-
OHT
OK1
P2P
RHI
RNS
RPM
RSF
SJN
TR2
TWZ
UPT
VH1
W2D
W8F
WH7
WHG
WOQ
X7M
Y6R
ZGI
ZXP
~KM
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
ID FETCH-LOGICAL-c450t-92b0f6d99a527e6ca25eb252638c5395f84140d0cbbe048e60c81d9ab52ff8e83
ISSN 0019-9567
1098-5522
IngestDate Thu Aug 21 17:36:38 EDT 2025
Fri Jul 11 05:28:04 EDT 2025
Thu Apr 03 07:08:01 EDT 2025
Thu Apr 24 22:50:14 EDT 2025
Tue Jul 01 02:09:17 EDT 2025
IsDoiOpenAccess false
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 9
Language English
License Copyright © 2015, American Society for Microbiology. All Rights Reserved.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c450t-92b0f6d99a527e6ca25eb252638c5395f84140d0cbbe048e60c81d9ab52ff8e83
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.
OpenAccessLink https://iai.asm.org/content/iai/83/9/3418.full.pdf
PMID 26056382
PQID 1704348398
PQPubID 23479
PageCount 10
ParticipantIDs pubmedcentral_primary_oai_pubmedcentral_nih_gov_4534658
proquest_miscellaneous_1704348398
pubmed_primary_26056382
crossref_primary_10_1128_IAI_00678_15
crossref_citationtrail_10_1128_IAI_00678_15
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2015-09-01
PublicationDateYYYYMMDD 2015-09-01
PublicationDate_xml – month: 09
  year: 2015
  text: 2015-09-01
  day: 01
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
– name: 1752 N St., N.W., Washington, DC
PublicationTitle Infection and immunity
PublicationTitleAlternate Infect Immun
PublicationYear 2015
Publisher American Society for Microbiology
Publisher_xml – name: American Society for Microbiology
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
SSID ssj0014448
Score 2.4955878
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...
SourceID pubmedcentral
proquest
pubmed
crossref
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 3418
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
URI https://www.ncbi.nlm.nih.gov/pubmed/26056382
https://www.proquest.com/docview/1704348398
https://pubmed.ncbi.nlm.nih.gov/PMC4534658
Volume 83
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3Nb9MwFLfKEIgLggGjfMlI7FRlpK6dxMfRgVpgE0KdKKcodh1qqSRVmxw2jvzjPCeOk8ImAZcoSpwP5ffLe37P7wOhV0ORghJg3OMqUB6lYeBFXBIPlHeiaGjW5oxr4PQsmJzT93M27_V-dqKWykIcycsr80r-B1U4BriaLNl_QNbdFA7APuALW0AYtn-F8Yn5QTNZmLw917mqis04U2WxyddLvaprMI_Hn8kheWN-4VxeFHVdh0_lCl7VhM2NTfOIKnkArj2xPVOKwYeVEltt4qMG60yVMFgnJvTQtJXYdqe1UxvSVUc26yrnpHDO-rm2cb-TUl8uc6srq4WPje0LYlFuPasflbapONPs20YvWq_tzHq4v2rvi9Jdr8WQubAsUDq1pDWFTBkjO6K47mljKcc7chV0bXS1wCcmiWF6PD2q9K5X54Z2sF9_r8A3ZhuIGtKqPReM2Jy6gW4SsDVI4_KxS1EUDNgmY4JEr7uPMpWk7cW705o_bJXfQ247c5jZPXTXGh_4uGbSfdRT2T66VbcjvdhHt09toMUD9KOhFt6hFs5T3KEWBrSxodYAO2LhIseOWNgRy1zpiIVbYuGWWNgS6yE6f_d2Np54tk-HJynzC48T4afBgvOEkVAFMiFMCcIIfBfJRpylEQUzfuFLIRQoDBX4EqwknghG0jRS0egR2svyTD1G2Cx6q0gmNIkU9YlIotGIcsHBzveZFFEfDZrPHEtbxN682yqujFkSxYBPXOETD1kfHbrR67p4yzXjXjaIxSBdzZJZkqm83MbD0KcjCkYEPPmgRtDdqYG-j8IdbN0AU7l990yml1UFdxCAFKb-T66951N0p_1rnqG9YlOq5zD7LcSLip2_AG3jsjc
linkProvider National Library of Medicine
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Distinct+Contributions+of+Neutrophils+and+CCR2%2B+Monocytes+to+Pulmonary+Clearance+of+Different+Klebsiella+pneumoniae+Strains&rft.jtitle=Infection+and+immunity&rft.au=Xiong%2C+Huizhong&rft.au=Carter%2C+Rebecca+A&rft.au=Leiner%2C+Ingrid+M&rft.au=Tang%2C+Yi-Wei&rft.date=2015-09-01&rft.eissn=1098-5522&rft.volume=83&rft.issue=9&rft.spage=3418&rft_id=info:doi/10.1128%2FIAI.00678-15&rft_id=info%3Apmid%2F26056382&rft.externalDocID=26056382
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0019-9567&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0019-9567&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0019-9567&client=summon