Negative energy balance alters global gene expression and immune responses in the uterus of postpartum dairy cows

被引:221
作者
Wathes, D. Claire [1 ]
Cheng, Zhangrui [1 ]
Chowdhury, Waliul [1 ]
Fenwick, Mark A. [1 ]
Fitzpatrick, Richard [2 ]
Morris, Dermot G. [2 ]
Patton, Joe [3 ]
Murphy, John J. [3 ]
机构
[1] Univ London Royal Vet Coll, Dept Vet Basic Sci, Reprod Grp, London, England
[2] Anim Prod Res Ctr, Athenry, County Galway, Ireland
[3] Dairy Prod Res Ctr, Fermoy, Cork, Ireland
基金
英国惠康基金;
关键词
microarray; bovine; endometrium; innate immune system; antimicrobial peptides; BOVINE BETA-DEFENSINS; BODY CONDITION SCORE; UTERINE INVOLUTION; INSULIN-RESISTANCE; 2-DIMENSIONAL ELECTROPHORESIS; PERIPARTUM PERIOD; EPITHELIAL-CELLS; AMNIOTIC-FLUID; HOST-DEFENSE; FATTY-ACIDS;
D O I
10.1152/physiolgenomics.00064.2009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Wathes DC, Cheng Z, Chowdhury W, Fenwick MA, Fitzpatrick R, Morris DG, Patton J, Murphy JJ. Negative energy balance alters global gene expression and immune responses in the uterus of postpartum dairy cows. Physiol Genomics 39: 1-13, 2009. First published June 30, 2009; doi: 10.1152/physiolgenomics.00064.2009.-Most dairy cows suffer uterine microbial contamination postpartum. Persistent endometritis often develops, associated with reduced fertility. We used a model of differential feeding and milking regimes to produce cows in differing negative energy balance status in early lactation (mild or severe, MNEB or SNEB). Blood hematology was assessed preslaughter at 2 wk postpartum. RNA expression in endometrial samples was compared using bovine Affymetrix arrays. Data were mapped using Ingenuity Pathway Analysis. Circulating concentrations of IGF-I remained lower in the SNEB group, whereas blood nonesterified fatty acid and beta-hydroxybutyrate concentrations were raised. White blood cell count and lymphocyte number were reduced in SNEB cows. Array analysis of endometrial samples identified 274 differentially expressed probes representing 197 recognized genes between the energy balance groups. The main canonical pathways affected related to immunological and inflammatory disease and connective tissue disorders. Inflammatory response genes with major upregulation in SNEB cows included matrix metalloproteinases, chemokines, cytokines, and calgranulins. Expression of several interferon-inducible genes including ISG20, IFIH1, MX1, and MX2 were also significantly increased in the SNEB cows. These results provide evidence that cows in SNEB were still undergoing an active uterine inflammatory response 2 wk postpartum, whereas MNEB cows had more fully recovered from their energy deficit, with their endometrium reaching a more advanced stage of repair. SNEB may therefore prevent cows from mounting an effective immune response to the microbial challenge experienced after calving, prolonging the time required for uterine recovery and compromising subsequent fertility.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 77 条
[1]  
[Anonymous], LOGICIEL RATIONNEMEN
[2]   PARTITIONING OF NUTRIENTS DURING PREGNANCY AND LACTATION - A REVIEW OF MECHANISMS INVOLVING HOMEOSTASIS AND HOMEORHESIS [J].
BAUMAN, DE ;
CURRIE, WB .
JOURNAL OF DAIRY SCIENCE, 1980, 63 (09) :1514-1529
[4]   Influence of body condition score on relationships between metabolic status and oxidative stress in periparturient dairy cows [J].
Bernabucci, U ;
Ronchi, B ;
Lacetera, N ;
Nardone, A .
JOURNAL OF DAIRY SCIENCE, 2005, 88 (06) :2017-2026
[5]  
Bondurant RH, 1999, J ANIM SCI, V77, P101
[6]   PERIPARTURIENT DISEASES AND THEIR EFFECT ON REPRODUCTIVE-PERFORMANCE IN 5 DAIRY HERDS [J].
BORSBERRY, S ;
DOBSON, H .
VETERINARY RECORD, 1989, 124 (09) :217-219
[7]   Energy balance relationships with follicular development, ovulation and fertility in postpartum dairy cows [J].
Butler, WR .
LIVESTOCK PRODUCTION SCIENCE, 2003, 83 (2-3) :211-218
[8]  
CAI TQ, 1994, AM J VET RES, V55, P934
[9]  
Cole AM, 2006, CURR TOP MICROBIOL, V306, P199
[10]   Antimicrobial polypeptides are key Anti-HIV-1 effector molecules of cervicovaginal host defense [J].
Cole, Alexander M. ;
Cole, Amy Liese .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2008, 59 (01) :27-34