Uterine microbial communities and their potential role in the regulation of epithelium cell cycle and apoptosis in aged hens

BackgroundAlterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are well-established in mammals. However, as representative oviparous animals, the research on the uterine microbial ecosystem and its functions with physiolo...

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Published inMicrobiome Vol. 11; no. 1; pp. 1 - 19
Main Authors Dai, Dong, Wang, Jing, Zhang, Haijun, Wu, Shugeng, Qi, Guanghai
Format Journal Article
LanguageEnglish
Published London BioMed Central 11.11.2023
BMC
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Abstract BackgroundAlterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are well-established in mammals. However, as representative oviparous animals, the research on the uterine microbial ecosystem and its functions with physiological homeostasis is limited in chickens. Additionally, continuous egg-laying disrupts the oviducal immune defenses of aged hens, susceptible to pathogen invasion, causing poor egg quality and food-borne infections in humans. Here, we investigated aging-related changes in the oviduct microbial colonization and transmission from the gut to eggs and their roles in a hen model.ResultsThe results of 16S rDNA sequencing showed significant differences in the oviduct microbial composition between young (38 weeks) and aged (77 weeks) laying hens. SourceTracker analysis further revealed differences in the effects of microbial transmission on the oviducal microbiota between young and aged hens. Enhanced barrier defense with cell apoptosis suppression and cell cycle arrest of the uterus were observed in aged hens reducing microbial transmission from the lower to upper reproductive tract. In addition, a total of 361 significantly differential metabolites were identified using metabolomics in the aged uterine microbiota, especially in products of amino acid metabolism and biosynthesis of various secondary metabolites, which might have essential effects on cell apoptosis by regulating immune responses and cell cycle. Notably, antibiotics disrupted uterine microbiota by dietary intervention and direct perfusion did not retard aging-related physiological changes but further aggravated aging processes by disrupting the cell cycle and apoptosis.ConclusionsThe microbiota continuum along the reproductive tract in aged birds differs from that in young birds, especially with a significant shift in the uterus. The aged uterine microbiota probably contributes to the regulation of cell cycle and apoptosis by microbial metabolites primarily involved in amino acid metabolism and biosynthesis of various secondary metabolites. These findings provide new insights into the roles of the reproductive tract microbiota in regulating the cell programming of the aged host, contributing to the exploration of the microbiome as a target for diagnosing aging health status and therapy for gynecological diseases in women.Video Abstract
AbstractList Abstract Background Alterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are well-established in mammals. However, as representative oviparous animals, the research on the uterine microbial ecosystem and its functions with physiological homeostasis is limited in chickens. Additionally, continuous egg-laying disrupts the oviducal immune defenses of aged hens, susceptible to pathogen invasion, causing poor egg quality and food-borne infections in humans. Here, we investigated aging-related changes in the oviduct microbial colonization and transmission from the gut to eggs and their roles in a hen model. Results The results of 16S rDNA sequencing showed significant differences in the oviduct microbial composition between young (38 weeks) and aged (77 weeks) laying hens. SourceTracker analysis further revealed differences in the effects of microbial transmission on the oviducal microbiota between young and aged hens. Enhanced barrier defense with cell apoptosis suppression and cell cycle arrest of the uterus were observed in aged hens reducing microbial transmission from the lower to upper reproductive tract. In addition, a total of 361 significantly differential metabolites were identified using metabolomics in the aged uterine microbiota, especially in products of amino acid metabolism and biosynthesis of various secondary metabolites, which might have essential effects on cell apoptosis by regulating immune responses and cell cycle. Notably, antibiotics disrupted uterine microbiota by dietary intervention and direct perfusion did not retard aging-related physiological changes but further aggravated aging processes by disrupting the cell cycle and apoptosis. Conclusions The microbiota continuum along the reproductive tract in aged birds differs from that in young birds, especially with a significant shift in the uterus. The aged uterine microbiota probably contributes to the regulation of cell cycle and apoptosis by microbial metabolites primarily involved in amino acid metabolism and biosynthesis of various secondary metabolites. These findings provide new insights into the roles of the reproductive tract microbiota in regulating the cell programming of the aged host, contributing to the exploration of the microbiome as a target for diagnosing aging health status and therapy for gynecological diseases in women. Video Abstract
BackgroundAlterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are well-established in mammals. However, as representative oviparous animals, the research on the uterine microbial ecosystem and its functions with physiological homeostasis is limited in chickens. Additionally, continuous egg-laying disrupts the oviducal immune defenses of aged hens, susceptible to pathogen invasion, causing poor egg quality and food-borne infections in humans. Here, we investigated aging-related changes in the oviduct microbial colonization and transmission from the gut to eggs and their roles in a hen model.ResultsThe results of 16S rDNA sequencing showed significant differences in the oviduct microbial composition between young (38 weeks) and aged (77 weeks) laying hens. SourceTracker analysis further revealed differences in the effects of microbial transmission on the oviducal microbiota between young and aged hens. Enhanced barrier defense with cell apoptosis suppression and cell cycle arrest of the uterus were observed in aged hens reducing microbial transmission from the lower to upper reproductive tract. In addition, a total of 361 significantly differential metabolites were identified using metabolomics in the aged uterine microbiota, especially in products of amino acid metabolism and biosynthesis of various secondary metabolites, which might have essential effects on cell apoptosis by regulating immune responses and cell cycle. Notably, antibiotics disrupted uterine microbiota by dietary intervention and direct perfusion did not retard aging-related physiological changes but further aggravated aging processes by disrupting the cell cycle and apoptosis.ConclusionsThe microbiota continuum along the reproductive tract in aged birds differs from that in young birds, especially with a significant shift in the uterus. The aged uterine microbiota probably contributes to the regulation of cell cycle and apoptosis by microbial metabolites primarily involved in amino acid metabolism and biosynthesis of various secondary metabolites. These findings provide new insights into the roles of the reproductive tract microbiota in regulating the cell programming of the aged host, contributing to the exploration of the microbiome as a target for diagnosing aging health status and therapy for gynecological diseases in women.Video Abstract
Alterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are well-established in mammals. However, as representative oviparous animals, the research on the uterine microbial ecosystem and its functions with physiological homeostasis is limited in chickens. Additionally, continuous egg-laying disrupts the oviducal immune defenses of aged hens, susceptible to pathogen invasion, causing poor egg quality and food-borne infections in humans. Here, we investigated aging-related changes in the oviduct microbial colonization and transmission from the gut to eggs and their roles in a hen model.BACKGROUNDAlterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are well-established in mammals. However, as representative oviparous animals, the research on the uterine microbial ecosystem and its functions with physiological homeostasis is limited in chickens. Additionally, continuous egg-laying disrupts the oviducal immune defenses of aged hens, susceptible to pathogen invasion, causing poor egg quality and food-borne infections in humans. Here, we investigated aging-related changes in the oviduct microbial colonization and transmission from the gut to eggs and their roles in a hen model.The results of 16S rDNA sequencing showed significant differences in the oviduct microbial composition between young (38 weeks) and aged (77 weeks) laying hens. SourceTracker analysis further revealed differences in the effects of microbial transmission on the oviducal microbiota between young and aged hens. Enhanced barrier defense with cell apoptosis suppression and cell cycle arrest of the uterus were observed in aged hens reducing microbial transmission from the lower to upper reproductive tract. In addition, a total of 361 significantly differential metabolites were identified using metabolomics in the aged uterine microbiota, especially in products of amino acid metabolism and biosynthesis of various secondary metabolites, which might have essential effects on cell apoptosis by regulating immune responses and cell cycle. Notably, antibiotics disrupted uterine microbiota by dietary intervention and direct perfusion did not retard aging-related physiological changes but further aggravated aging processes by disrupting the cell cycle and apoptosis.RESULTSThe results of 16S rDNA sequencing showed significant differences in the oviduct microbial composition between young (38 weeks) and aged (77 weeks) laying hens. SourceTracker analysis further revealed differences in the effects of microbial transmission on the oviducal microbiota between young and aged hens. Enhanced barrier defense with cell apoptosis suppression and cell cycle arrest of the uterus were observed in aged hens reducing microbial transmission from the lower to upper reproductive tract. In addition, a total of 361 significantly differential metabolites were identified using metabolomics in the aged uterine microbiota, especially in products of amino acid metabolism and biosynthesis of various secondary metabolites, which might have essential effects on cell apoptosis by regulating immune responses and cell cycle. Notably, antibiotics disrupted uterine microbiota by dietary intervention and direct perfusion did not retard aging-related physiological changes but further aggravated aging processes by disrupting the cell cycle and apoptosis.The microbiota continuum along the reproductive tract in aged birds differs from that in young birds, especially with a significant shift in the uterus. The aged uterine microbiota probably contributes to the regulation of cell cycle and apoptosis by microbial metabolites primarily involved in amino acid metabolism and biosynthesis of various secondary metabolites. These findings provide new insights into the roles of the reproductive tract microbiota in regulating the cell programming of the aged host, contributing to the exploration of the microbiome as a target for diagnosing aging health status and therapy for gynecological diseases in women. Video Abstract.CONCLUSIONSThe microbiota continuum along the reproductive tract in aged birds differs from that in young birds, especially with a significant shift in the uterus. The aged uterine microbiota probably contributes to the regulation of cell cycle and apoptosis by microbial metabolites primarily involved in amino acid metabolism and biosynthesis of various secondary metabolites. These findings provide new insights into the roles of the reproductive tract microbiota in regulating the cell programming of the aged host, contributing to the exploration of the microbiome as a target for diagnosing aging health status and therapy for gynecological diseases in women. Video Abstract.
ArticleNumber 251
Author Qi, Guanghai
Zhang, Haijun
Dai, Dong
Wu, Shugeng
Wang, Jing
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Cites_doi 10.1080/19490976.2021.1907270
10.1038/s12276-020-0375-3
10.1016/j.foodcont.2021.107996
10.1038/nmeth.1650
10.1093/nar/gky299
10.1016/j.nbt.2015.03.006
10.1128/spectrum.00462-22
10.1016/j.mad.2021.111587
10.1038/s41587-019-0209-9
10.1186/s40168-018-0470-z
10.1093/gigascience/giab067
10.1186/s40168-021-01184-w
10.1111/j.1574-6976.2008.00161.x
10.1093/bioinformatics/bty560
10.1006/meth.2001.1262
10.1038/s42255-021-00348-0
10.1186/s12864-020-07177-7
10.1016/j.psj.2021.101104
10.1038/nm934
10.1016/j.cell.2016.10.020
10.1159/000490615
10.1016/j.psj.2022.102008
10.1038/s41582-019-0244-7
10.1016/j.ejmech.2018.11.025
10.1111/IGC.0b013e3181a41613
10.3389/fcimb.2021.649067
10.1002/ijc.33428
10.1016/S0031-3203(02)00060-2
10.1080/19490976.2020.1857505
10.3389/fimmu.2018.00208
10.18129/B9.bioc.topGO
10.24272/j.issn.2095-8137.2020.382
10.3389/fmicb.2020.01508
10.1038/nmeth.3317
10.1038/s43587-021-00093-9
10.1038/s41396-022-01253-4
10.1016/j.trecan.2020.01.019
10.3389/fnut.2021.692305
10.1038/s41416-019-0620-5
10.3168/jds.2019-17106
10.1093/nar/gks1219
10.1038/nbt.3122
10.1016/j.dld.2018.02.012
10.1038/nature06247
10.1093/ps/85.11.1969
10.1038/nm1196
10.1038/mi.2010.77
10.1186/1471-2105-12-323
10.1038/s41467-021-24516-8
10.1093/gigascience/giy107
10.1128/mmbr.00181-21
10.1016/j.cyto.2018.09.015
10.1007/s00253-022-12089-5
10.1038/nrc3535
10.1038/s41585-020-0286-z
10.1038/s41580-020-00314-w
10.1038/nrmicro3344
10.3382/ps/pez118
10.1038/s43587-022-00294-w
10.1080/1040841X.2021.1944052
10.1016/j.tim.2005.01.002
10.1186/s13045-023-01453-1
10.1016/j.tim.2019.07.006
10.1002/pmic.201900408
10.1186/s13059-014-0550-8
10.1186/s40168-021-01208-5
10.1016/j.psj.2020.12.005
10.1038/s41467-017-00901-0
10.1038/nature24661
10.1080/19490976.2022.2038865
10.1016/j.immuni.2015.04.019
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References M Boehme (1707_CR70) 2021; 1
T Wilmanski (1707_CR60) 2021; 3
KN Galvão (1707_CR7) 2019; 102
M Elhamouly (1707_CR14) 2019; 98
W Berry (1707_CR52) 2006; 85
M Schirmer (1707_CR41) 2016; 167
D Knights (1707_CR25) 2011; 8
H Liu (1707_CR22) 2022; 16
C Chen (1707_CR5) 2017; 8
KJ Livak (1707_CR35) 2001; 25
D Dai (1707_CR12) 2022; 101
L Yang (1707_CR63) 2023; 16
I Moreno (1707_CR2) 2022; 10
L Yang (1707_CR11) 2021; 100
J Feng (1707_CR13) 2020; 21
MI Love (1707_CR31) 2014; 15
N Sun (1707_CR20) 2021; 11
K Jaye (1707_CR58) 2022; 14
JM Baker (1707_CR3) 2018; 9
S Karakashev (1707_CR50) 2021; 42
FT Liu (1707_CR16) 2022; 10
X Shi (1707_CR73) 2022; 106
S Amat (1707_CR17) 2022; 854453
RN Morgan (1707_CR55) 2022; 48
T Wilmanski (1707_CR69) 2022; 2
S Kim (1707_CR40) 2018; 64
P Łaniewski (1707_CR6) 2020; 17
R Di Micco (1707_CR42) 2021; 22
P Louis (1707_CR59) 2014; 12
AJ Muller (1707_CR66) 2005; 11
M Pekmezovic (1707_CR38) 2019; 27
S Chen (1707_CR27) 2018; 34
OO Coker (1707_CR65) 2022; 10
KS Kudryashova (1707_CR49) 2020; 20
AP Bhavsar (1707_CR54) 2007; 449
1707_CR33
Y Guo (1707_CR39) 2020; 12
M Barrett (1707_CR57) 2020; 6
MN Anahtar (1707_CR37) 2015; 42
C Uyttenhove (1707_CR67) 2003; 9
EL Lieu (1707_CR61) 2020; 52
J Wang (1707_CR1) 2021; 12
NA Bokulich (1707_CR23) 2018; 6
P Sansonetti (1707_CR71) 2011; 4
Y Hou (1707_CR48) 2019; 15
C Quast (1707_CR24) 2012; 41
C Binda (1707_CR46) 2018; 50
B Li (1707_CR30) 2011; 12
D Dodd (1707_CR64) 2017; 551
I Gantois (1707_CR8) 2009; 33
B Zhu (1707_CR4) 2022; 86
Z Xu (1707_CR72) 2019; 162
N Shterzer (1707_CR36) 2020; 11
MS Kuyukina (1707_CR44) 2015; 32
A Likas (1707_CR32) 2003; 36
L Vettore (1707_CR62) 2020; 122
M Elhamouly (1707_CR43) 2018; 111
Q Lin (1707_CR9) 2021; 125
M Pertea (1707_CR29) 2015; 33
D Dai (1707_CR34) 2021; 8
W Lu (1707_CR53) 2021; 148
Y Su (1707_CR10) 2021; 10
C Wen (1707_CR18) 2021; 100
JP Nougayrède (1707_CR56) 2005; 13
L Zhang (1707_CR47) 2021; 200
A Zavatta (1707_CR15) 2022; 64
F Li (1707_CR19) 2018; 7
E Bolyen (1707_CR21) 2019; 37
Y Darzi (1707_CR26) 2018; 46
PA Johnson (1707_CR51) 2013; 13
T Wilmanski (1707_CR68) 2021; 13
D Kim (1707_CR28) 2015; 12
A Barua (1707_CR45) 2009; 19
References_xml – volume: 13
  start-page: 1907270
  issue: 1
  year: 2021
  ident: 1707_CR68
  publication-title: Gut Microbes
  doi: 10.1080/19490976.2021.1907270
– volume: 52
  start-page: 15
  issue: 1
  year: 2020
  ident: 1707_CR61
  publication-title: Exp Mol Med
  doi: 10.1038/s12276-020-0375-3
– volume: 125
  start-page: 107996
  year: 2021
  ident: 1707_CR9
  publication-title: Food Control
  doi: 10.1016/j.foodcont.2021.107996
– volume: 8
  start-page: 761
  issue: 9
  year: 2011
  ident: 1707_CR25
  publication-title: Nat Methods
  doi: 10.1038/nmeth.1650
– volume: 46
  start-page: W510
  issue: W1
  year: 2018
  ident: 1707_CR26
  publication-title: Nucleic Acids Res
  doi: 10.1093/nar/gky299
– volume: 32
  start-page: 559
  issue: 6
  year: 2015
  ident: 1707_CR44
  publication-title: New Biotechnol
  doi: 10.1016/j.nbt.2015.03.006
– volume: 10
  start-page: e00462
  issue: 3
  year: 2022
  ident: 1707_CR16
  publication-title: Microbiol Spectr
  doi: 10.1128/spectrum.00462-22
– volume: 200
  start-page: 111587
  year: 2021
  ident: 1707_CR47
  publication-title: Mech Ageing Dev
  doi: 10.1016/j.mad.2021.111587
– volume: 37
  start-page: 852
  issue: 8
  year: 2019
  ident: 1707_CR21
  publication-title: Nat Biotechnol
  doi: 10.1038/s41587-019-0209-9
– volume: 6
  start-page: 1
  issue: 1
  year: 2018
  ident: 1707_CR23
  publication-title: Microbiome
  doi: 10.1186/s40168-018-0470-z
– volume: 10
  start-page: giab067
  issue: 9
  year: 2021
  ident: 1707_CR10
  publication-title: GigaScience
  doi: 10.1093/gigascience/giab067
– volume: 10
  start-page: 1
  year: 2022
  ident: 1707_CR2
  publication-title: Microbiome
  doi: 10.1186/s40168-021-01184-w
– volume: 33
  start-page: 718
  issue: 4
  year: 2009
  ident: 1707_CR8
  publication-title: FEMS Microbiol Rev
  doi: 10.1111/j.1574-6976.2008.00161.x
– volume: 34
  start-page: i884
  issue: 17
  year: 2018
  ident: 1707_CR27
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/bty560
– volume: 854453
  start-page: 13
  year: 2022
  ident: 1707_CR17
  publication-title: Front Microbiol
– volume: 25
  start-page: 402
  issue: 4
  year: 2001
  ident: 1707_CR35
  publication-title: Methods
  doi: 10.1006/meth.2001.1262
– volume: 3
  start-page: 274
  issue: 2
  year: 2021
  ident: 1707_CR60
  publication-title: Nat Metab
  doi: 10.1038/s42255-021-00348-0
– volume: 21
  start-page: 1
  issue: 1
  year: 2020
  ident: 1707_CR13
  publication-title: BMC Genomics
  doi: 10.1186/s12864-020-07177-7
– volume: 100
  start-page: 101104
  issue: 7
  year: 2021
  ident: 1707_CR18
  publication-title: Poult Sci
  doi: 10.1016/j.psj.2021.101104
– volume: 9
  start-page: 1269
  issue: 10
  year: 2003
  ident: 1707_CR67
  publication-title: Nat Med
  doi: 10.1038/nm934
– volume: 167
  start-page: 1125
  issue: 4
  year: 2016
  ident: 1707_CR41
  publication-title: Cell
  doi: 10.1016/j.cell.2016.10.020
– volume: 64
  start-page: 513
  issue: 6
  year: 2018
  ident: 1707_CR40
  publication-title: Gerontology
  doi: 10.1159/000490615
– volume: 101
  start-page: 102008
  issue: 9
  year: 2022
  ident: 1707_CR12
  publication-title: Poult Sci
  doi: 10.1016/j.psj.2022.102008
– volume: 15
  start-page: 565
  issue: 10
  year: 2019
  ident: 1707_CR48
  publication-title: Nat Rev Neurol
  doi: 10.1038/s41582-019-0244-7
– volume: 162
  start-page: 266
  year: 2019
  ident: 1707_CR72
  publication-title: Eur J Med Chem
  doi: 10.1016/j.ejmech.2018.11.025
– volume: 19
  start-page: 531
  issue: 4
  year: 2009
  ident: 1707_CR45
  publication-title: Int J Gynecol Cancer
  doi: 10.1111/IGC.0b013e3181a41613
– volume: 11
  start-page: 649067
  year: 2021
  ident: 1707_CR20
  publication-title: Front Cell Infect Mi
  doi: 10.3389/fcimb.2021.649067
– volume: 148
  start-page: 1708
  issue: 7
  year: 2021
  ident: 1707_CR53
  publication-title: Int J Cancer
  doi: 10.1002/ijc.33428
– volume: 36
  start-page: 451
  issue: 2
  year: 2003
  ident: 1707_CR32
  publication-title: Pattern Recogn
  doi: 10.1016/S0031-3203(02)00060-2
– volume: 12
  start-page: 1857505
  issue: 1
  year: 2020
  ident: 1707_CR39
  publication-title: Gut Microbes
  doi: 10.1080/19490976.2020.1857505
– volume: 9
  start-page: 208
  year: 2018
  ident: 1707_CR3
  publication-title: Front Immunol
  doi: 10.3389/fimmu.2018.00208
– ident: 1707_CR33
  doi: 10.18129/B9.bioc.topGO
– volume: 42
  start-page: 153
  issue: 2
  year: 2021
  ident: 1707_CR50
  publication-title: Zool Res
  doi: 10.24272/j.issn.2095-8137.2020.382
– volume: 11
  start-page: 1508
  year: 2020
  ident: 1707_CR36
  publication-title: Front Microbiol
  doi: 10.3389/fmicb.2020.01508
– volume: 12
  start-page: 357
  issue: 4
  year: 2015
  ident: 1707_CR28
  publication-title: Nat Methods
  doi: 10.1038/nmeth.3317
– volume: 1
  start-page: 666
  issue: 8
  year: 2021
  ident: 1707_CR70
  publication-title: Nat Aging
  doi: 10.1038/s43587-021-00093-9
– volume: 16
  start-page: 2040
  issue: 8
  year: 2022
  ident: 1707_CR22
  publication-title: ISME J
  doi: 10.1038/s41396-022-01253-4
– volume: 6
  start-page: 277
  issue: 4
  year: 2020
  ident: 1707_CR57
  publication-title: Trends Cancer
  doi: 10.1016/j.trecan.2020.01.019
– volume: 8
  start-page: 692305
  year: 2021
  ident: 1707_CR34
  publication-title: Front Nutr
  doi: 10.3389/fnut.2021.692305
– volume: 122
  start-page: 150
  issue: 2
  year: 2020
  ident: 1707_CR62
  publication-title: Brit J Cancer
  doi: 10.1038/s41416-019-0620-5
– volume: 102
  start-page: 11786
  issue: 12
  year: 2019
  ident: 1707_CR7
  publication-title: J Dairy Sci
  doi: 10.3168/jds.2019-17106
– volume: 41
  start-page: D590
  issue: D1
  year: 2012
  ident: 1707_CR24
  publication-title: Nucleic Acids Res
  doi: 10.1093/nar/gks1219
– volume: 33
  start-page: 290
  issue: 3
  year: 2015
  ident: 1707_CR29
  publication-title: Nat Biotechnol
  doi: 10.1038/nbt.3122
– volume: 50
  start-page: 421
  issue: 5
  year: 2018
  ident: 1707_CR46
  publication-title: Digest Liver Dis
  doi: 10.1016/j.dld.2018.02.012
– volume: 449
  start-page: 827
  issue: 7164
  year: 2007
  ident: 1707_CR54
  publication-title: Nature
  doi: 10.1038/nature06247
– volume: 85
  start-page: 1969
  issue: 11
  year: 2006
  ident: 1707_CR52
  publication-title: Poult Sci
  doi: 10.1093/ps/85.11.1969
– volume: 64
  start-page: 1
  year: 2022
  ident: 1707_CR15
  publication-title: Clin Rev Allerg Immu
– volume: 11
  start-page: 312
  issue: 3
  year: 2005
  ident: 1707_CR66
  publication-title: Nat Med
  doi: 10.1038/nm1196
– volume: 4
  start-page: 8
  issue: 1
  year: 2011
  ident: 1707_CR71
  publication-title: Mucosal Immunol
  doi: 10.1038/mi.2010.77
– volume: 12
  start-page: 323
  year: 2011
  ident: 1707_CR30
  publication-title: BMC Bioinformatics
  doi: 10.1186/1471-2105-12-323
– volume: 12
  start-page: 4191
  issue: 1
  year: 2021
  ident: 1707_CR1
  publication-title: Nat Commun
  doi: 10.1038/s41467-021-24516-8
– volume: 7
  start-page: giy107
  issue: 10
  year: 2018
  ident: 1707_CR19
  publication-title: Gigascience
  doi: 10.1093/gigascience/giy107
– volume: 86
  start-page: e00181
  issue: 4
  year: 2022
  ident: 1707_CR4
  publication-title: Microbiol Mol Biol R
  doi: 10.1128/mmbr.00181-21
– volume: 111
  start-page: 303
  year: 2018
  ident: 1707_CR43
  publication-title: Cytokine
  doi: 10.1016/j.cyto.2018.09.015
– volume: 106
  start-page: 1
  year: 2022
  ident: 1707_CR73
  publication-title: Appl Microbiol Biot
  doi: 10.1007/s00253-022-12089-5
– volume: 13
  start-page: 432
  issue: 6
  year: 2013
  ident: 1707_CR51
  publication-title: Nat Rev Cancer
  doi: 10.1038/nrc3535
– volume: 17
  start-page: 232
  issue: 4
  year: 2020
  ident: 1707_CR6
  publication-title: Nat Rev Urol
  doi: 10.1038/s41585-020-0286-z
– volume: 22
  start-page: 75
  issue: 2
  year: 2021
  ident: 1707_CR42
  publication-title: Nat Rev Mol Cell Bio
  doi: 10.1038/s41580-020-00314-w
– volume: 12
  start-page: 661
  issue: 10
  year: 2014
  ident: 1707_CR59
  publication-title: Nat Rev Microbiol
  doi: 10.1038/nrmicro3344
– volume: 98
  start-page: 3022
  issue: 7
  year: 2019
  ident: 1707_CR14
  publication-title: Poult Sci
  doi: 10.3382/ps/pez118
– volume: 2
  start-page: 869
  issue: 10
  year: 2022
  ident: 1707_CR69
  publication-title: Nat Aging
  doi: 10.1038/s43587-022-00294-w
– volume: 48
  start-page: 42
  issue: 1
  year: 2022
  ident: 1707_CR55
  publication-title: Crit Rev Microbiol
  doi: 10.1080/1040841X.2021.1944052
– volume: 13
  start-page: 103
  issue: 3
  year: 2005
  ident: 1707_CR56
  publication-title: Trends Microbiol
  doi: 10.1016/j.tim.2005.01.002
– volume: 16
  start-page: 59
  issue: 1
  year: 2023
  ident: 1707_CR63
  publication-title: J Hematol Oncol
  doi: 10.1186/s13045-023-01453-1
– volume: 27
  start-page: 982
  issue: 12
  year: 2019
  ident: 1707_CR38
  publication-title: Trends Microbiol
  doi: 10.1016/j.tim.2019.07.006
– volume: 20
  start-page: e1900408
  issue: 5–6
  year: 2020
  ident: 1707_CR49
  publication-title: Proteomics
  doi: 10.1002/pmic.201900408
– volume: 15
  start-page: 550
  issue: 12
  year: 2014
  ident: 1707_CR31
  publication-title: Genome Biol
  doi: 10.1186/s13059-014-0550-8
– volume: 10
  start-page: 1
  issue: 1
  year: 2022
  ident: 1707_CR65
  publication-title: Microbiome
  doi: 10.1186/s40168-021-01208-5
– volume: 100
  start-page: 100892
  issue: 3
  year: 2021
  ident: 1707_CR11
  publication-title: Poult Sci
  doi: 10.1016/j.psj.2020.12.005
– volume: 8
  start-page: 875
  issue: 1
  year: 2017
  ident: 1707_CR5
  publication-title: Nat Commun
  doi: 10.1038/s41467-017-00901-0
– volume: 551
  start-page: 648
  issue: 7682
  year: 2017
  ident: 1707_CR64
  publication-title: Nature
  doi: 10.1038/nature24661
– volume: 14
  start-page: 2038865
  issue: 1
  year: 2022
  ident: 1707_CR58
  publication-title: Gut Microbes
  doi: 10.1080/19490976.2022.2038865
– volume: 42
  start-page: 965
  issue: 5
  year: 2015
  ident: 1707_CR37
  publication-title: Immunity
  doi: 10.1016/j.immuni.2015.04.019
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Snippet BackgroundAlterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are...
Alterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are well-established in...
Abstract Background Alterations of the uterine microbiome are closely associated with various intrauterine diseases and physiological conditions, which are...
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SubjectTerms Aging
Amino acids
Animals
Antibiotics
Apoptosis
Biosynthesis
Cell cycle
Cytokines
Deoxyribonucleic acid
Diet
Discriminant analysis
DNA
Egg laying
Enzymes
Epithelium
Feeds
Food quality
Gynecological diseases
Hen
Homeostasis
Immune response
Immunoglobulins
Metabolites
Metabolomics
Microbial metabolite
Microbiome
Microbiomes
Microbiota
Oviduct
Physiology
Proteins
Reproductive system
Roles
rRNA 16S
Secondary metabolites
Senescence
Uterus
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Title Uterine microbial communities and their potential role in the regulation of epithelium cell cycle and apoptosis in aged hens
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Volume 11
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