Abstract
The aim of the present study was to quantify the number of immune cells infiltrated in the endometrium of endometritis gilts. Based on gross morphology, a selected 28 genital organs of endometritis gilts were investigated. The gilts were classified according to the ovarian appearance into three groups, i.e. follicular, luteal, and ovarian quiescent phases. Historical data, reason for culling, histopathology, bacterial identification, and number and type of immune cells in different layers of the endometrium were examined. The gilts were culled at 336 ± 63 days of age at a body weight of 142 ± 20 kg. The culling reasons included abnormal vaginal discharge (n = 10), repeat breeding (n = 6), anestrus (n = 6), abortion (n = 4), and not pregnant (n = 2). Bacteria identified from pus exudates included Escherichia coli (33.3%), Staphylococcus sp. (17.5%), α-hemolytic Streptococcus sp. (14.3%), and β-hemolytic Streptococcus sp. (9.5%). Neutrophils were the most common immune cells in the epithelial and subepithelial tissue layers of the endometrium, while lymphocytes were the most common immune cells in the glandular layer. Neutrophils in the epithelial and subepithelial layers of the endometrium in the luteal phase were lower than in the follicular and ovarian quiescent phase. During the acute stage, neutrophils were the most common immune cells in the endometrium, while during the chronic stages, lymphocytes, plasma cells, and eosinophils were the dominant immune cells. In conclusion, the number and type of immune cells in the endometrium of the endometritis gilts varied according to both the reproductive cycles and the stage of endometritis. Neutrophils, lymphocytes, plasma cells, and eosinophils indicate stages and the severity of endometritis.
Similar content being viewed by others
References
Althouse GC, Lu KG (2005) Bacteriospermia in extended porcine semen. Theriogenology 63:573–584
Bara MR, McGowan MR, O’Boyle D, Cameron RDA (1993) A study of the microbial flora of the anterior vagina of normal sows during different stages of the reproductive cycle. Aus Vet J 70:256–259
Barrow GI, Feltham RKA (1993) Cowan and Steel’s manual for the identification of medical bacteria, 3rd edn. Great Britain at the University Press, Cambridge 331 pp
Carabin H, Martineau G-P, Vaillancourt D, Higgins R, Bigras-Poulin M (1996) Detection of cervical bacterial contamination in swine by two methods of swabbing in relation to artificial insemination. Can J Vet Res 60:40–44
Dalin A-M, Gidlund K, Eliasson-Selling L (1997) Post-mortem examination of genital organs from sows with reproductive disturbances in a sow-pool. Acta Vet Scand 38:253–262
Dalin A-M, Kaeoket K, Persson E (2004) Immune cell infiltration of normal and impaired sow endometrium. Anim Reprod Sci 82–83:401–413
De Winter PJJ, Verdonck M, De Kruif A, Devriese LA, Haesebrouck F (1994) Influence of the estrus cycle on experimental intrauterine E. coli infection in the sow. J Vet Med A 41:640–644
De Winter PJJ, Verdonck M, De Kruif A, Devriese LA, Haesebrouck F (1995) Bacterial endometritis and vaginal discharge in the sow: prevalence of different bacterial species and experimental reproduction of the syndrome. Anim Reprod Sci 37:325–335
Dial GD, MacLachlan NJ (1988) Urogenital infections of swine. Part I. Clinical manifestations and pathogenesis. Compendium Food Animal 10:63–69
Engblom L, Lundeheim N, Dalin A-M, Andersson K (2007) Sow removal in Swedish commercial herds. Livest Sci 106:76–86
Heinonen M, Leppävuori A, Pyörälä S (1998) Evaluation of reproductive failure of female pigs based on slaughterhouse material and herd record survey. Anim Reprod Sci 52:235–244
Jana B, Kucharski J, Ziecik AJ (2004) Effect of intrauterine infusion of Escherichia coli on hormonal patterns in gilts during the estrus cycle. Reprod Nutr Dev 44:37–48
Jana B, Kucharski J, Dzienis A, Deptula K (2007) Changes in prostaglandin production and ovarian function in gilts during endometritis infuced by Escherichia coli infection. Anim Reprod Sci 97:137–150
Jiwakanon J, Persson E, Dalin A-M (2006) The endometrium of the anoestrous female pig: studies on infiltration by cells of the immune system. Reprod Domest Anim 41:191–195
Kaeoket K, Persson E, Dalin A-M (2001) The sow endometrium at different stages of the oestrus cycle: studies on morphological changes and infiltration by cells of the immune system. Anim Reprod Sci 65:95–114
Kaeoket K, Tantasuparuk W, Kunavongkrit A (2005) The effect of post-ovulatory insemination on the subsequent embryonic loss, oestrus cycle length and vaginal discharge in sows. Reprod Domest Anim 40:492–494
Kaeoket K, Tantasuparuk W, Kunavongkrit A (2006) Induction of endometritis in sows by post-ovulatory insemination. Proc 19th IPVS, 16–19 July 2006, Copenhagen, Denmark. 2006 Volume 2: 484
Karlberg K, Rein KA, Nordstoga K (1981) Histological and bacteriological examination of uterus from the repeat breeder gilts and sows. Nord Vet-Med 33:359–365
Lucia T Jr, Dial GD, Marsh WE (2000) Lifetime reproductive performance in female pigs having distinct reasons for removal. Livest Prod Sci 63:213–222
MacLachlan NJ, Dial GD (1987) An epizootic of endometritis in gilts. Vet Pathol 24:92–94
Maes D, Nauwynck H, Rijsselaere T, Mateusen B, Vyt P, de Kruif A, Van Soom A (2008) Diseases in swine transmitted by artificial insemination: an overview. Theriogenology 70:1337–1345
Muirhead MR (1986) Epidemiology and control of vaginal discharge in the sow after service. Vet Rec 199:233–235
Roberson J, Moll D, Saunder G (2007) Chronic Staphylococcus aureus endometritis in virgin gilt. Vet Rec 161:821–822
SAS (2002) SAS/Stat® User’s guide (Release 9.0). SAS Inst. Inc., Cary
Teankum K, Pospischil A, Janett F, Burgi E, Brugnera E, Hoelzle K, Polkinghorne A, Weilenmann R, Zimmermann DR, Borel N (2006) Detection of chlamydiae in boar semen and genital tracts. Vet Micro 116:149–157
Tummaruk P, Sukamphaichit N, Kitiarpornchai W, Musikjearanan S, Tantasuparuk W (2006) Seasonal influence on causes of culling in gilts. Proc 19th IPVS Congress, Copenhagen, Denmark, p 498
Tummaruk P, Tantasuparuk W, Techakumphu M, Kunavongkrit A (2007) Age, BW and backfat thickness at first-observed estrus in crossbred Landrace x Yorkshire gilts, seasonal variations and their influence on subsequence reproductive performance. Anim Reprod Sci 99:167–181
Tummaruk P, Kesdangsakonwut S, Kunavongkrit A (2009) Relationships among specific reason for culling, reproductive data and gross-morphology of the genital tracts in gilts culled due to reproductive failure in Thailand. Theriogenology 71:369–375
Wulster-Radeliffe MC, Seals RC, Lewis GS (2003) Progesterone increase susceptibility of gilts to uterine infections after intrauterine inoculation with infection bacteria. J Anim Sci 81:1242–1252
Acknowledgements
The present study was funded by the Thailand Research Fund (MRG4880127). Thanks go to Mr. Supradit Wangnaithum and Mrs. Pussadee Makum for their technical support. Finally, we would also like to thank Assistant Prof. Simon Wright and Chula Unisearch, Chulalongkorn University for linguistic scrutinization.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Tummaruk, P., Kesdangsakonwut, S., Prapasarakul, N. et al. Endometritis in gilts: reproductive data, bacterial culture, histopathology, and infiltration of immune cells in the endometrium. Comp Clin Pathol 19, 575–584 (2010). https://doi.org/10.1007/s00580-009-0929-1
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00580-009-0929-1