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Infection and immunity1985; 48(1); 94-108; doi: 10.1128/iai.48.1.94-108.1985

Morphology of three strains of contagious equine metritis organism.

Abstract: Examination of recently isolated cultures of three strains of Contagious Equine Metritis Organism grown on specially formulated, serum-free, clear typing medium revealed the presence of numerous colonial opacity variants. These colonies were prepared by a number of fixation and staining techniques and examined by scanning and transmission electron microscopy. Opaque and transparent phenotypes produced copious amounts of extracellular material compared with intermediate-opacity phenotypes which produced little or none. Also unique to intermediate colonies were numerous thin intercellular strands, which may represent pili or polymers of extracellular material. The presence of an unusual fibrillar layer (with similar electron density to the extracellular material) on the outer leaf of the outer membrane also was confirmed. A number of other ultrastructural features also were noted, including an epilayer, a thin nonmembranous layer which covered colonies and adjacent agar.
Publication Date: 1985-04-01 PubMed ID: 3838532PubMed Central: PMC261920DOI: 10.1128/iai.48.1.94-108.1985Google Scholar: Lookup
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  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research study focuses on the detailed examination of three strains of Contagious Equine Metritis Organism (CEMO) to identify and analyze their different characteristics, especially in terms of colonial opacity variants and extracellular material production.

Objective and Methods of the Study

  • The study’s primary focus was to investigate the morphology of three strains of Contagious Equine Metritis Organism (CEMO), an infection that can be sexually transmitted amongst horses.
  • The researchers cultivated these cultures on a specialized, serum-free, clear typing medium.
  • The researchers used various fixation and staining techniques to prepare the colonies for examination.
  • Both scanning and transmission electron microscopy, powerful tools for visualizing biological samples at high resolution, were used to study the cultures.
  • Findings of the Study

    • During examination, the researchers noticed a high number of colonial opacity variants in the cultures.
    • The opaque and transparent phenotypes were found to yield more extracellular material than the phenotypes with intermediate-opacity. The latter produced little to no extracellular material.
    • The researchers also noticed unique thin strands connecting cells (intercellular) in intermediate colonies. These may either be pili (hair-like structures on the surface of many bacteria) or polymers of extracellular material according to the researchers.
    • Findings on Ultrastructural Features

      • Upon further examination, the researchers also noticed an unusual fibrillar layer with similar electron density to the extracellular material, on the outer leaf of the outer membrane.
      • Other ultrastructural features worth noting were the epilayer, a thin nonmembranous layer that covered colonies and adjacent agar.
      • However, the abstract does not provide detail about the implications of these ultrastructural features.

      Conclusion

      • This research provides in-depth knowledge on the morphological characteristics of Contagious Equine Metritis Organism and paves the way for future studies to understand the pathogenesis of the disease and potentially define therapeutic strategies.

Cite This Article

APA
Hitchcock PJ, Brown TM, Corwin D, Hayes SF, Olszewski A, Todd WJ. (1985). Morphology of three strains of contagious equine metritis organism. Infect Immun, 48(1), 94-108. https://doi.org/10.1128/iai.48.1.94-108.1985

Publication

ISSN: 0019-9567
NlmUniqueID: 0246127
Country: United States
Language: English
Volume: 48
Issue: 1
Pages: 94-108

Researcher Affiliations

Hitchcock, P J
    Brown, T M
      Corwin, D
        Hayes, S F
          Olszewski, A
            Todd, W J

              MeSH Terms

              • Animals
              • Bacterial Infections / microbiology
              • Bacterial Infections / veterinary
              • Culture Media
              • Endometritis / microbiology
              • Endometritis / veterinary
              • Female
              • Gram-Negative Bacteria / cytology
              • Gram-Negative Bacteria / growth & development
              • Gram-Negative Bacteria / ultrastructure
              • Horse Diseases / microbiology
              • Horses
              • Microscopy, Electron
              • Phenotype
              • Sexually Transmitted Diseases / microbiology
              • Sexually Transmitted Diseases / veterinary

              References

              This article includes 41 references
              1. Swanson J, Barrera O. Gonococcal pilus subunit size heterogeneity correlates with transitions in colony piliation phenotype, not with changes in colony opacity.. J Exp Med 1983 Nov 1;158(5):1459-72.
                pubmed: 6138388doi: 10.1084/jem.158.5.1459google scholar: lookup
              2. Blake MS, Gotschlich EC. Purification and partial characterization of the opacity-associated proteins of Neisseria gonorrhoeae.. J Exp Med 1984 Feb 1;159(2):452-62.
                pubmed: 6420502doi: 10.1084/jem.159.2.452google scholar: lookup
              3. Sherwood JE, Vasse JM, Dazzo FB, Truchet GL. Development and trifoliin A-binding ability of the capsule of Rhizobium trifolii.. J Bacteriol 1984 Jul;159(1):145-52.
                pubmed: 6376470doi: 10.1128/jb.159.1.145-152.1984google scholar: lookup
              4. Todd WJ, Wray GP, Hitchcock PJ. Arrangement of pili in colonies of Neisseria gonorrhoeae.. J Bacteriol 1984 Jul;159(1):312-20.
                pubmed: 6145701doi: 10.1128/jb.159.1.312-320.1984google scholar: lookup
              5. LAWN AM. The use of potassium permanganate as an electron-dense stain for sections of tissue embedded in epoxy resin.. J Biophys Biochem Cytol 1960 Feb;7(1):197-8.
                pubmed: 14414705doi: 10.1083/jcb.7.1.197google scholar: lookup
              6. Good NE, Winget GD, Winter W, Connolly TN, Izawa S, Singh RM. Hydrogen ion buffers for biological research.. Biochemistry 1966 Feb;5(2):467-77.
                pubmed: 5942950doi: 10.1021/bi00866a011google scholar: lookup
              7. Sutton JS. Potassium permanganate staining of ultrathin sections for electron microscopy.. J Ultrastruct Res 1967 Dec;21(5):424-9.
                pubmed: 4173347doi: 10.1016/s0022-5320(67)80150-3google scholar: lookup
              8. Spurr AR. A low-viscosity epoxy resin embedding medium for electron microscopy.. J Ultrastruct Res 1969 Jan;26(1):31-43.
                pubmed: 4887011doi: 10.1016/s0022-5320(69)90033-1google scholar: lookup
              9. Kellogg DS Jr, Cohen IR, Norins LC, Schroeter AL, Reising G. Neisseria gonorrhoeae. II. Colonial variation and pathogenicity during 35 months in vitro.. J Bacteriol 1968 Sep;96(3):596-605.
                pubmed: 4979098doi: 10.1128/jb.96.3.596-605.1968google scholar: lookup
              10. Jephcott AE, Reyn A, Birch-Andersen A. Neisseria gonorrhoeae 3. Demonstration of presumed appendages to cells from different colony types.. Acta Pathol Microbiol Scand B Microbiol Immunol 1971;79(3):437-9.
              11. Palumbo SA, Johnson MG, Rieck VT, Witter LD. Growth measurements on surface colonies of bacteria.. J Gen Microbiol 1971 May;66(2):137-43.
                pubmed: 5571859doi: 10.1099/00221287-66-2-137google scholar: lookup
              12. Swanson J, Kraus SJ, Gotschlich EC. Studies on gonococcus infection. I. Pili and zones of adhesion: their relation to gonococcal growth patterns.. J Exp Med 1971 Oct 1;134(4):886-906.
                pubmed: 4106489doi: 10.1084/jem.134.4.886google scholar: lookup
              13. Luft JH. Ruthenium red and violet. I. Chemistry, purification, methods of use for electron microscopy and mechanism of action.. Anat Rec 1971 Nov;171(3):347-68.
                pubmed: 4108333doi: 10.1002/ar.1091710302google scholar: lookup
              14. Swanson J. Studies on gonococcus infection. IV. Pili: their role in attachment of gonococci to tissue culture cells.. J Exp Med 1973 Mar 1;137(3):571-89.
                pubmed: 4631989doi: 10.1084/jem.137.3.571google scholar: lookup
              15. Silva MT, Sousa JC. Ultrastructure of the cell wall and cytoplasmic membrane of gram-negative bacteria with different fixation techniques.. J Bacteriol 1973 Feb;113(2):953-62.
                pubmed: 4120570doi: 10.1128/jb.113.2.953-962.1973google scholar: lookup
              16. Brew K, Shaper JH, Olsen KW, Trayer IP, Hill RL. Cross-linking of the components of lactose synthetase with dimethylpimelimidate.. J Biol Chem 1975 Feb 25;250(4):1434-44.
                pubmed: 234456
              17. Buchanan TM. Antigenic heterogeneity of gonococcal pili.. J Exp Med 1975 Jun 1;141(6):1470-5.
                pubmed: 805212doi: 10.1084/jem.141.6.1470google scholar: lookup
              18. Malick LE, Wilson RB. Modified thiocarbohydrazide procedure for scanning electron microscopy: routine use for normal, pathological, or experimental tissues.. Stain Technol 1975 Jul;50(4):265-9.
                pubmed: 1103373doi: 10.3109/10520297509117069google scholar: lookup
              19. Walstad DL, Guymon LF, Sparling PF. Altered outer membrane protein in different colonial types of Neisseria gonorrhoeae.. J Bacteriol 1977 Mar;129(3):1623-7.
                pubmed: 403181doi: 10.1128/jb.129.3.1623-1627.1977google scholar: lookup
              20. Matsumoto A, Fujiwara E, Higashi N. Observations of the surface projections of infectious small cell of Chlamydia psittaci in thin sections.. J Electron Microsc (Tokyo) 1976;25(3):169-70.
                pubmed: 799722
              21. Ito S, Vinson JW, McGuire TJ Jr. Murine typhus Rickettsiae in the Oriental rat flea.. Ann N Y Acad Sci 1975;266:35-60.
              22. James JF, Swanson J. Studies on gonococcus infection. XIII. Occurrence of color/opacity colonial variants in clinical cultures.. Infect Immun 1978 Jan;19(1):332-40.
                pubmed: 415007doi: 10.1128/iai.19.1.332-340.1978google scholar: lookup
              23. Taylor CE, Rosenthal RO, Brown DF, Lapage SP, Hill LR, Legros RM. The causative organism of contagious equine metritis 1977: proposal for a new species to be known as Haemophilus equigenitalis.. Equine Vet J 1978 Jul;10(3):136-44.
              24. Swanson J. Studies on gonococcus infection. XIV. Cell wall protein differences among color/opacity colony variants of Neisseria gonorrhoeae.. Infect Immun 1978 Jul;21(1):292-302.
                pubmed: 101459doi: 10.1128/iai.21.1.292-302.1978google scholar: lookup
              25. Timoney PJ, O'Reilly PJ, McArdle JF, Ward J, Harrington AM. Responses of mares to rechallenge with the organism of contagious equine metritis 1977.. Vet Rec 1979 Mar 24;104(12):264.
                pubmed: 473508doi: 10.1136/vr.104.12.264google scholar: lookup
              26. Reyrolle J, Letellier F. Autoradiographic study of the localization and evolution of growth zones in bacterial colonies.. J Gen Microbiol 1979 Apr;111(2):399-406.
                pubmed: 479831doi: 10.1099/00221287-111-2-399google scholar: lookup
              27. Timoney PJ, O'Reilly PJ, McArdle JF, Ward J, Harrington AM, McCormack R. Responses of pony mares to the agent of contagious equine metritis 1977.. J Reprod Fertil Suppl 1979;(27):367-75.
                pubmed: 289811
              28. Eaglesome MD, Garcia MM. Contagious equine metritis: a review.. Can Vet J 1979 Aug;20(8):201-6.
                pubmed: 389400
              29. Lambden PR, Robertson JN, Watt PJ. Biological properties of two distinct pilus types produced by isogenic variants of Neisseria gonorrhoeae P9.. J Bacteriol 1980 Jan;141(1):393-6.
                pubmed: 6101593doi: 10.1128/jb.141.1.393-396.1980google scholar: lookup
              30. Salit IE, Blake M, Gotschlich EC. Intra-strain heterogeneity of gonococcal pili is related to opacity colony variance.. J Exp Med 1980 Mar 1;151(3):716-25.
                pubmed: 6102108doi: 10.1084/jem.151.3.716google scholar: lookup
              31. Swaney LM, Breese SS Jr. Ultrastructure of Haemophilus equigenitalis, causative agent of contagious equine metritis.. Am J Vet Res 1980 Jan;41(1):127-32.
                pubmed: 7362118
              32. Lambden PR, Heckels JE, James LT, Watt PJ. Variations in surface protein composition associated with virulence properties in opacity types of Neisseria gonorrhoeae.. J Gen Microbiol 1979 Oct;114(2):305-12.
                pubmed: 120407doi: 10.1099/00221287-114-2-305google scholar: lookup
              33. Fernie DS, Batty I, Walker PD, Platt H, Mackintosh ME, Simpson DJ. Observations on vaccine and post-infection immunity in contagious equine metritis.. Res Vet Sci 1980 May;28(3):362-7.
                pubmed: 7414090
              34. Sahu SP, Dardiri AH. Contagious equine metritis: isolation and characterization of the etiologic agent.. Am J Vet Res 1980 Sep;41(9):1379-82.
                pubmed: 7447130
              35. Sahu SP. Contagious equine metritis: effect of vaccination on control of the disease.. Am J Vet Res 1981 Jan;42(1):45-8.
                pubmed: 7224317
              36. Powell DG. Contagious equine metritis.. Adv Vet Sci Comp Med 1981;25:161-84.
                pubmed: 7034499
              37. Sahu SP, Weber S. Contagious equine metritis: effect of intrauterine inoculation of tiny colony forms in pony mares.. Vet Rec 1982 Mar 13;110(11):250-1.
                pubmed: 7080411doi: 10.1136/vr.110.11.250google scholar: lookup
              38. Sahu SP, Wool S, Breese SS Jr. Observation on the morphology of contagious equine metritis bacterial colonies isolated from infected pony mares.. Am J Vet Res 1982 May;43(5):796-800.
                pubmed: 7091842
              39. Swanson J. Colony opacity and protein II compositions of gonococci.. Infect Immun 1982 Jul;37(1):359-68.
                pubmed: 6809633doi: 10.1128/iai.37.1.359-368.1982google scholar: lookup
              40. Goldman RC, White D, Orskov F, Orskov I, Rick PD, Lewis MS, Bhattacharjee AK, Leive L. A surface polysaccharide of Escherichia coli O111 contains O-antigen and inhibits agglutination of cells by O-antiserum.. J Bacteriol 1982 Sep;151(3):1210-21.
              41. Timoney PJ, Shin SJ, Jacobson RH. Improved selective medium for isolation of the contagious equine metritis organism.. Vet Rec 1982 Jul 31;111(5):107-8.
                pubmed: 7123830doi: 10.1136/vr.111.5.107google scholar: lookup

              Citations

              This article has been cited 5 times.
              1. He Y, Zhang S, Zhang Y, Wu B, Xue Y, Ye C, Li Q, Olivia AN, Tembo JM, Chen H, Cai H, Chen T. Distinct Patterns of Host Adherence by Neisseria gonorrhoeae Isolated from Experimental Gonorrhea.. Can J Infect Dis Med Microbiol 2021;2021:7865405.
                doi: 10.1155/2021/7865405pubmed: 34093925google scholar: lookup
              2. Hébert L, Moumen B, Pons N, Duquesne F, Breuil MF, Goux D, Batto JM, Laugier C, Renault P, Petry S. Genomic characterization of the Taylorella genus.. PLoS One 2012;7(1):e29953.
                doi: 10.1371/journal.pone.0029953pubmed: 22235352google scholar: lookup
              3. Munderloh UG, Madigan JE, Dumler JS, Goodman JL, Hayes SF, Barlough JE, Nelson CM, Kurtti TJ. Isolation of the equine granulocytic ehrlichiosis agent, Ehrlichia equi, in tick cell culture.. J Clin Microbiol 1996 Mar;34(3):664-70.
                doi: 10.1128/jcm.34.3.664-670.1996pubmed: 8904434google scholar: lookup
              4. Swanson J, Bergström S, Barrera O, Robbins K, Corwin D. Pilus- gonococcal variants. Evidence for multiple forms of piliation control.. J Exp Med 1985 Aug 1;162(2):729-44.
                doi: 10.1084/jem.162.2.729pubmed: 2410533google scholar: lookup
              5. Pincus SH, Cole RL, Wessels MR, Corwin MD, Kamanga-Sollo E, Hayes SF, Cieplak W Jr, Swanson J. Group B streptococcal opacity variants.. J Bacteriol 1992 Jun;174(11):3739-49.