Inflammatory responses to induced infectious endometritis in mares resistant or susceptible to persistent endometritis
详细信息    查看全文
  • 作者:Mette Christoffersen (1)
    Elizabeth Woodward (2)
    Anders M Bojesen (3)
    Stine Jacobsen (4)
    Morten R Petersen (1)
    Mats HT Troedsson (2)
    Henrik Lehn-Jensen (1)
  • 关键词:Infectious endometritis ; Susceptibility ; Cytokines ; Serum amyloid A
  • 刊名:BMC Veterinary Research
  • 出版年:2012
  • 出版时间:December 2012
  • 年:2012
  • 卷:8
  • 期:1
  • 全文大小:341KB
  • 参考文献:1. Dimock W, Edwards P: Pathology and bacteriology of the reproductive organs of mares in relation to sterility. / Kentucky Agricultural Experiment Station Bulletin (Research Bulletin) 1928, 286:157-37.
    2. Wingfield Digby N, Ricketts S: Results of concurrent bacteriological and cytological examinations of the endometrium of mares in routine stud farm practice. / J Reprod Fertil Suppl 1982, 32:181-85.
    3. Adams G, Kastelic J, Bergfelt D, Ginther O: Effect of uterine inflammation and ultrasonically-detected uterine pathology on fertility in the mare. / J Reprod Fertil 1987,35(suppl):445-54.
    4. Hughes J, Loy R: Investigations on the effect of intrauterine inoculations of Streptococcus zooepidemicus in the mare. / Proc 15th Ann Conv Am Assoc Eq Pract 1969, 289-92.
    5. Peterson FB, McFeely RA, David JSE: Studies on the pathogenesis of endometritis in the mare. / Proc 15th Ann Conv Am Assoc Eq Pract 1969, 279-87.
    6. Troedsson MHT: Breeding-induced endometritis in mares. / Vet Clin N Am -equine 2006,22(3):705-12. CrossRef
    7. Kotilainen T, Huhtinen M, Katila T: Sperm-induced leukocytosis in the equine uterus. / Theriogenology 1994,41(3):629-36. CrossRef
    8. Troedsson MHT, Crabo BG, Ibrahim N, Scott M, Ing M: Mating-induced endometritis: mechanisms, clinical importance and consequences [abstract]. / Proc Am Assoc Equine Pract 1994, 41:11-2.
    9. Christoffersen M, Baagoe CD, Jacobsen S, Bojesen AM, Petersen MR, Lehn-Jensen H: Evaluation of the systemic acute phase response and endometrial gene expression of serum amyloid A and pro- and anti-inflammatory cytokines in mares with experimentally induced endometritis. / Vet Immunol Immunop 2010,138(1-):95-05. CrossRef
    10. Nash DM, Sheldon IM, Herath S, Lane EA: Markers of the uterine innate immune response of the mare. / Anim Reprod Sci 2010, 119:31-9. CrossRef
    11. Fumuso EA, Giguire S, Wade J, Rogan D, Videla-Dorna I, Bowden RA: Endometrial IL-1[beta], IL-6 and TNF-[alpha], mRNA expression in mares resistant or susceptible to post-breeding endometritis: effects of estrous cycle, artificial insemination and immunomodulation. / Vet Immunol Immunop 2003,96(1-):31-1. CrossRef
    12. Fumuso EA, Aguilar J, Giguire S, Rivulgo M, Wade J, Rogan D: Immune parameters in mares resistant and susceptible to persistent post-breeding endometritis: effects of immunomodulation. / Vet Immunol Immunop 2007,118(1-):30-9. CrossRef
    13. Troedsson MHT: Uterine response to semen deposition in the mare. In / Proc Soc Theriogenology. San Antonio, TX; 1995:130-35.
    14. Asbury A: Uterine defense mechanisms in the mare: the use of intrauterine plasma in the management of endometritis. / Theriogenology 1983, 21:387-93. CrossRef
    15. Widders P, Stokes C, David J, Bourne F: Quantification of the immunoglobulins in reproductive tract secretion in the mare. / Res Vet Sci 1984, 37:324-30.
    16. Evans MJ, Hamer JM, Gason LM, Graham CS, Asbury AC, Irvine CHG: Clearance of bacteria and non-antigenic markers following intra-uterine inoculation into maiden mares: effect of steroid hormone environment. / Theriogenology 1986,26(1):37-0. CrossRef
    17. Troedsson MHT, Liu IKM: Uterine clearance of non-antigenic markers (Cr 51 ) in response to a bacterial challenge in mares potentially susceptible and resistant to chronic uterine infection. / J Reprod Fertil 1991, 44:283-88.
    18. Troedsson MHT, Liu IKM: Multiple site electromyography recordings of uterine activity following an intrauterine bacterial challenge in mares susceptible and resistant to chronic uterine infection. / J Reprod Fertil 1993, 99:307-13. CrossRef
    19. Battut I, Colchen S, Fieni F, Tainturier D, Bruyas JF: Succes rates when attempting to nonsurgically collect equine embryos at 144, 156 or 168 hours after ovulation. / Equine Vet J 1997,25(Suppl):60-2.
    20. Orsi N, Tribe R: Cytokine networks and the regulation of uterine function in pregnancy and parturition. / J Neuroendocrinol 2008, 20:462-69. CrossRef
    21. Kenney RM, Doig PA: Equine Endometrial Biopsy. In / Current therapy in Theriogenology: Diagnosis, Treatment, and Prevention of Reproductive Diseases in Small and Large Animals. / Volume 2. Edited by: Marrow D, Marrow D. Philadelphia: W.B. Saunders; 1986:723-29.
    22. Troedsson MHT, Alghamdi AM, Matissen J: Equine seminal plasma protects the fertility of spermatozoa in an inflamed uterine environment. / Theriogenology 2002,58(2-):453-56. CrossRef
    23. Nielsen J: Endometritis in the mare: a diagnostic study comparing cultures from swab and biopsy. / Theriogenology 2005,64(3):510-18. CrossRef
    24. Jacobsen S, Kjelgaard-Hansen M, Hagbard Petersen H, Jensen AL: Evaluation of a commercially available human serum amyloid A (SAA) turbidometric immunoassay for determination of equine SAA concentrations. / Vet J 2006,172(2):315-19. CrossRef
    25. Berg LC, Jacobsen S, Dybdahl-Thomsen P: Local production of serum amyloid A in equine articular cartilage and cultured chondrocytes. In / Proceedings of the 6th European Colloquium on Acute Phase Proterins. Edited by: Jacobsen S, Kjelgaard-Hansen M. Copenhagen, Denmark: Samfundslitteratur; 2006.
    26. Iqbal J, Bird JL, Hollander AP, Bayliss MT: Effect of matrix depleting agents on the expression of chondrocyte metabolism by equine chondrocytes. / Res Vet Sci 2004,77(3):249-56. CrossRef
    27. Quinlivan M, Nelly M, Prendergast M, Breathnach C, Horohov D, Arkins S, Chiang YW, Chu HJ, Ng T, Cullinane A: Pro-inflammatory and antiviral cytokine expression in vaccinated and unvaccinated horses exposed to equine influenza virus. / Vaccine 2007,25(41):7056-064. CrossRef
    28. Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F: Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. / Genome Biol 2002,3(7):1-2. CrossRef
    29. Robinson TL, Sutherland IA, Sutherland J: Validation of candidate bovine reference genes for use with real-time PCR. / Vet Immunol Immunopathol 2007,115(1-):160-65. CrossRef
    30. Livak KJ, Schmittgen TD: Analysis of relative gene expression data using real-time quantitative PCR and the 2-[Delta][Delta]CT method. / Methods 2001,25(4):402-08. CrossRef
    31. Palm F, Walter I, Budik S, Kolodziejek J, Nowotny N, Aurich C: Influence of different semen extenders and seminal plasma on PMN migration and on expression of IL-1[beta], IL-6, TNF-[alpha] and COX-2 mRNA in the equine endometrium. / Theriogenology 2008,70(5):843-51. CrossRef
    32. Dinarello CA: Interleukin-1 and interleukin-1 antagonism. / Blood 1991,77(8):1627-652.
    33. Couper KN, Blount DG, Riley EM: IL-10: the master regulator of immunity to infection. / J Immunol 2008,180(9):5771-777.
    34. Arend WP, Guthridge CJ: Biological role of interleukin 1 receptor antagonist isoforms. / Ann Rheum Dis 2000, 59:60-4. CrossRef
    35. Couper KN, Blount DG, Riley EM: IL-10: the master regulator of immunity to infection. / J Immunol 2008,180(9):5771-777.
    36. Steel DM, Whitehead AS: The major acute phase reactants: C-reactive protein, serum amyloid P component and serum amyloid A protein. / Immunol Today 1994,15(2):81-8. CrossRef
    37. Raynes JG, Eagling S, McAdam PWJ: Acute-phase protein synthesis in human hepatoma cells: differential regulation of serum amyloid A (SAA) and haptoglobin by interleukin-1 and interleukin-6. / Clin Exp Immunol 1991, 83:488-91. CrossRef
    38. Herath S, Fischer DP, Werling D, Williams EJ, Lilly ST, Dobson H, Bryant CE, Sheldon IM: Expression and function of toll-like receptor 4 in the endometrial cells of the uterus. / Endocrinology 2006,147(1):562-70. CrossRef
    39. Herath S, Lilly ST, Santos NR, Gilbert RO, Goetze L, Bryant CE, White JO, Cronin J, Sheldon IM: Expression of genes associated with immunity in the endometrium of cattle with disparte postpartum uterine disease and fertility. / Reprod Biol Endocrinol 2009, 7:1-3. CrossRef
    40. Gabler C, Drillich M, Fischer C, Holder C, Heuwieser W, Einspanier R: Endometrial expression of selected transcripts involved in prostaglandin synthesis in cows with endometritis. / Theriogenology 2009,71(6):993-004. CrossRef
    41. LeBlanc MM, Neuwirth L, Asbury AC: Scintigraphic measurement of uterine clearance in normal mares and mares with recurrent endometritis. / Equine Vet J 1994, 26:109-13. CrossRef
    42. Troedsson MHT: Uterine clearance and resistance to persistent endometritis in the mare. / Theriogenology 1999,52(3):461-71. CrossRef
    43. Baggiolini M, Walz A, Kunkel SL: Neutrophil-activating peptide-1/Interleukin 8, a novel cytokine that activates neutrophils. / J Clin Invest 1989, 84:1045-049. CrossRef
    44. Troedsson MHT, Liu IKM, Ing M, Pascoe J: Smooth muscle electrical activity in the oviduct and the effect of oxytocin, PGF2α and PGE2 on the myometrium and the oviduct of the cycling mare. / Biol Reprod Mono 1995, 1:439-52.
    45. Tizard I: Neutrophils and their products. In / Veterinary Immunology -An introduction. / Volume 8. Edited by: Tizard I. St. Louis: Saunders Elsevier; 2009:28-0.
    46. Troedsson MH, Liu IK, Thurmond M: Function of uterine and blood-derived polymorphonuclear neutrophils in mares susceptible and resistant to chronic uterine infection: phagocytosis and chemotaxis. / Biol Reprod 1993,49(3):507-14. CrossRef
    47. Casini-Raggi V, Kam L, Chong YJ, Fiocchi C, Pizarro TT, Cominelli F: Mucosal imbalance of IL-1 and IL-1 receptor antagonist in inflammatory bowel disease. A novel mechanism of chronic intestinal inflammation. / J Immunol 1995,154(5):2434-440.
    48. Hinrichs K, Cummings M, Sertich P, Kenney R: Clinical significance of aerobic bacterial flora of the uterus, vagina, vestibule and clitoral fossa of clinically normal mares. / J Med Vet Med Assoc 1988, 193:72-5.
    49. Nikolakopoulos E, Watson ED: Uterine contractility is necessary for the clearance of intrauterine fluid but not bacteria after bacterial infusion in the mare. / Theriogenology 1999,52(3):413-23. CrossRef
    50. Broome AW, Winter AJ, McNutt SH, Casida LE: Variations in uterine response to experimental infection due to hormonal state of the ovaries. II. The mobilization of leukocytes and their importance in uterine bactericidal activity. / Am J Vet Res 1960, 21:675.
    51. Petersen MR, Nielsen JM, Lehm-Jensen H, Bojesen AM: Streptococcus equi subspecies zooepidemicus resides deep in the chronically infected endometrium of mares. / Clin Theriogenology 2009, 1:393-09.
    52. Güvenc K, Reilas T, Katila T: Effect of insemination dose and site on uterine inflammatory response of mares. / Theriogenology 2005,63(9):2504-512. CrossRef
    53. Watson ED, Stokes CR, Bourne FJ: Effect of exogenous ovarian steroids on the uterine luminal prostaglandins in ovarectomised mares with experimental endometritis. / Res Vet Sci 1988,44(3):361-65.
    54. Cadario ME, Thatcher MJ, LeBlanc MM: Relationship between prostaglandin and uterine clearance of radiocolloid in the mare. / Biol Reprod Mono 1995, 1:495-00.
    55. Alghamdi AS, Foster DN, Carlson CS, Troedsson MHT: Nitric oxide levels and nitric oxide synthase expression in uterine samples from mares susceptible and resistant to persistent breeding-induced endometritis. / Am J Reprod Immunol 2005, 53:230-37. CrossRef
    56. Li DJ, Liu YF, Li Y, Lv Y, Pei XY, Guo DZ: Significance of nitric oxide concentration in plasma and uterine secretes with puerperal endometritis in dairy cows. / Vet Res Commun 2010,34(4):315-21. CrossRef
    57. Yallampalli C, Garfield RE, Byam-Smith M: Nitric oxide inhibits uterine contractility during pregnancy but not during delivery. / Endocrinology 1993,133(4):1899-902. CrossRef
    58. Troedsson MHT, DeMoraes MJ, Liu IKM: Correlations between histologic endometrial lesions in mares and clinical response to intrauterine exposure with Streptococcus zooepidemicus . / Am J Vet Res 1993,54(4):570-72.
    59. Boosman R, Niewold T, Mutsaers C, Gruys E: Serum Amyloid A concentrations in cows given endotoxin as an acute-phase stimulant. / Am J Vet Res 1989, 50:1690-694.
    60. Hirvonen J, Eklund K, Teppo AM, Huszenicza G, Kulcsar M, Saloniemi H, Pyorala S: Acute phase response in dairy cows with experimentally induced Escherichia coli mastitis. / Acta Vet 1999, 40:35-6.
    61. Dabrowski R, Wawron W, Kostro K: Changes in CRP, SAA and haptoglobin produced in response to ovariohysterectomy in healthy bitches and those with pyometra. / Theriogenology 2007,67(2):321-27. CrossRef
    62. Sheldon IM, Noakes DE, Rycroft A, Dobson H: Acute phase protein responses to uterine bacterial contamination in cattle after calving. / Vet Rec 2001,148(6):172-75. CrossRef
    63. Huzzey JM, Duffield TF, LeBlanc SJ, Veira DM, Weary DM, von Keyserlingk MAG: Short communication: haptoglobin as an early indicator of metritis. / J Dairy Sci 2009,92(2):621-25. CrossRef
    64. Jacobsen S, Andersen PH, Toelboell T, Heegaard PMH: Dose dependency and individual variability of the lipopolysaccharide-induced bovine acute phase protein response. / J Dairy Sci 2004,87(10):3330-339. CrossRef
    65. Regassa F, Noakes DE: Acute phase protein response of ewes and the release of PGFM in relation to uterine involution and the presence of intrauterine bacteria. / Vet Rec 1999,144(18):502-06. CrossRef
    66. Hunt JS, Miller L, Roby KF, Huang J, Sue Platt J, DeBrot BL: Female steroid hormones regulate production of pro-inflammatory molecules in uterine leukocytes. / J Reprod Immunol 1997,35(2):87-9. CrossRef
    67. Pycock J: Infertility in the mare. In / Arthur's Veterinary Reproduction and Obstetrics. / Volume 8. Edited by: Noakes DE, Parkinson TJ, England GCW. Philadelphia: Saunders; 2001:577-21.
  • 作者单位:Mette Christoffersen (1)
    Elizabeth Woodward (2)
    Anders M Bojesen (3)
    Stine Jacobsen (4)
    Morten R Petersen (1)
    Mats HT Troedsson (2)
    Henrik Lehn-Jensen (1)

    1. Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Dyrlaegevej 68, Frederiksberg, Copenhagen, DK-1870, Denmark
    2. The Maxwell H. Gluck Equine Research Center, University of Kentucky, Lexington, KY, USA
    3. Department of Veterinary Disease Biology, Faculty of Health and Medical Sciences, University of Copenhagen, Stigboejlen 4, Frederiksberg, Copenhagen, DK-1870, Denmark
    4. Department of Large Animal Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Hoejbakkegaards Alle 5, Taastrup, DK-2630, Denmark
文摘
Background The objective of the study was to evaluate the gene expression of inflammatory cytokines (interleukin [IL]-1β, IL-6, IL-8, IL-10, tumor necrosis factor [TNF]-α, IL-1 receptor antagonist [ra] and serum amyloid A (SAA) in endometrial tissue and circulating leukocytes in response to uterine inoculation of 105 colony forming units (CFU) Escherichia coli in mares. Before inoculation, mares were classified as resistant or susceptible to persistent endometritis based on their uterine inflammatory response to infusion of 109 killed spermatozoa and histological assessment of the endometrial quality. Endometrial biopsies were obtained 3, 12, 24 and 72 hours (h) after bacterial inoculation and blood samples were obtained during the 7 day period post bacterial inoculation. Expression levels of cytokines and SAA were determined by quantitative real-time reverse transcriptase PCR (qRT-PCR). Results Compared to levels in a control biopsy (obtained in the subsequent estrous), resistant mares showed an up-regulation of IL-1β, IL-6, IL-8 and TNF-α at 3 h after E. coli inoculation, while susceptible mares showed increased gene expression of IL-6 and IL-1ra. Susceptible mares had a significant lower gene expression of TNF-α,IL-6 and increased expression of IL-1ra 3 h after E. coli inoculation compared to resistant mares. Susceptible mares showed a sustained and prolonged inflammatory response with increased gene expression levels of IL-1β, IL-8, IL-1ra and IL-1β:IL-1ra ratio throughout the entire study period (72 h), whereas levels in resistant mares returned to estrous control levels by 12 hours. Endometrial mRNA transcripts of IL-1β and IL-1ra were significantly higher in mares with heavy uterine bacterial growth compared to mares with no/mild growth. All blood parameters were unaffected by intrauterine E. coli infusion, except for a lower gene expression of IL-10 at 168 h and an increased expression of IL-1ra at 48 h observed in susceptible mares compared to resistant mares. Conclusions The current investigation suggests that endometrial mRNA transcripts of pro-inflammatory cytokines in response to endometritis are finely regulated in resistant mares, with initial high expression levels followed by normalization within a short period of time. Susceptible mares had a prolonged expression of pro-inflammatory cytokines, supporting the hypothesis that an unbalanced endometrial gene expression of inflammatory cytokines might play an important role in the pathogenesis of persistent endometritis.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700