Diagnostic method for bacterial vaginosis based on detecting antibodies against gvh toxin of gardnerella vaginalis

• US 20040101918A1
• Filed: 10/20/2003
• Published: 05/27/2004
• Est. Priority Date: 02/15/2001
• Status: Abandoned Application

• Current Assignee: Unibio S.R.L.
• Original Assignee: Unibio S.R.L.
• Inventors: Cauci, Sabina
• Application Number:
  US10/470,690
• Publication Number:
  US 20040101918A1
• Time in Patent Office: Days
• US Class Current: 435/7.32
• CPC Class Codes: G01N 33/56911 Bacteria

Abstract

The current invention relates to a method for the determination of the risk of pathologies in a population of women colonized by the Gardnerella vaginalis bacterium, comprising the following steps in order:

a) determination of the IgA and/or IgG and/or IgM antibody levels against Gvh toxin secreted by G. vaginalis in a sample of body fluid;

b) comparison of said levels of IgA and/or IgG and/or IgM with predeterminate levels of IgA and/or IgG and/or IgM, respectively;

c) determination of the risk factor.

Said method resulted particularly efficient in permitting to obtain an accurate and reliable evaluation of the risk of pathologies related to the colonization by the bacterium G. vaginalis in women. Consequently, this method gives the physician an effective tool to decide whether or not to administer a pharmacological therapy.

Claims

1. A method for the determination of the risk of pathologies in a population of women colonized by Gardnerella vaginalis bacterium, comprising the following steps in order:

a) determination of the levels of IgA and/or IgG and/or IgM antibodies against the Gvh toxin secreted by G. vaginalis in a sample of body fluid;

b) comparison of said levels of IgA and/or IgG and/or IgM with prefixed levels of IgA and/or IgG and/or IgM, respectively;

c) determination of risk factor.

2. Method as set forth in claim 1, furthermore comprising after the b) step:

determination of pH of the sample;

comparison of the measured pH value with a prefixed value.

3. Method as set forth in claim 1, furthermore comprising after the b) step:

determination of samples derived from women suffering BV.

4. Method as set forth in claim 1, furthermore comprising after the b) step:

determination of the bacterial flora in said samples of vaginal fluid.

5. Method as set forth in claim 1, furthermore comprising after the b) step:

determination of sialidase activity in said sample.

6. Method as set forth in claim 1, furthermore comprising after the b) step:

determination of prolidase activity in said sample.

7. Method as set forth in claim 1, furthermore comprising after the b) step:

determination of sialidase and prolidase activity in said sample.

8. Method as set forth in claim 1, in which the pathologies correlated with the colonization of the Gardnerella vaginalis bacterium comprise pregnancy adverse outcomes as low birth weight (LBW) or preterm delivery (PTD), preterm rupture of membranes, spontaneous abortion, infections of the amniotic fluid, post-partum endometritis, mother-to-child transmission of HIV infection, acquisition of HIV viral infection, and of HPV viral infection, upper genital tract infections (PID), post-partum ad post-gynecologic surgery infections, endometritis, cervitis.

9. Method as set forth in claim 1, in which the prefixed IgA value is 780 mOD, the prefixed IgG value is 740 mOD, the prefixed IgM value is 600 mOD, and the prefixed pH value is 4.7.

10. Method as set forth in claim 2, in which the prefixed IgA or IgG or IgM value is twofold the cutoff measured on healthy population and calculated from the medium value plus one standard deviation, and the prefixed pH is equal or over 4.7.

11. Method as set forth claim 1, in which said method is performed in a body fluid sample of women from the first to the second trimester of gestation.

12. Method as set forth in claim 11, in which said method is performed in a body fluid sample of women from the seventh to the twenty-fourth week'"'"' gestation.

13. Method as set forth in claim 1, in which said method is performed in a vaginal fluid sample of women.

14. Method as set forth in claim 13, in which said method is performed in a vaginal fluid sample of pregnant women.

15. Method as set forth in claim 1, in which the population of women colonized by G. vaginalis is constituted by pregnant women.

16. Method as set forth in claim 1, in which the population of women colonized by G. vaginalis is constituted by fertile age women.

17. Method as set forth in claim 1, in which the population of women colonized by G. vaginalis is constituted by postmenopausal women.

18. Method as set forth in claim 1, in which the determination of the IgA and/or IgG and/or IgM levels is carried out with a suitable immune enzymatic analysis comprising the availability, as antigen, of the Gvh toxin isolated from a suitable culture broth of G. vaginalis by precipitation comprising the following steps:

1) to draw a predetermined amount of G. vaginalis culture broth or of said toxin purified by chromatography of the supernatant of G. vaginalis culture broth, to chill and keep said amount at a temperature from 0 to +8°

C. for about 1 hour;

2) to add to said amount a determinate amount of precipitating agent at a final concentration that varies from 5 to 70% of the final volume;

3) to keep on ice for 30-60 minutes;

4) to centrifuge at a temperature from 0 to +8°

C. at 2500-5000 rpm for about 30-60 minutes in a way to obtain a supernatant and a pellet;

5) to eliminate the supernatant and then the precipitating agent remaining on the pellet;

6) to resuspend the pellet with sterile deionized water.

19. Method as set forth in claim 18, in which said precipitating agent is chosen in a group comprising methanol, ethanol, acetone, ammonium sulfate, propanol, isopropanol.

20. Method as set forth in claim 19, in which the precipitating agent is methanol at a concentration 33% of the final volume.

21. Method as set forth in claim 18, in which if the phase of IgA and/or IgG and/or IgM determination comprises the drawing of a predetermine amount of broth directly from the culture, then to the f) step a further precipitation follows repeating the step from b) to f).

22. Method as set forth in claim 18, in which at the end of the f) step the pellet is resuspended with AcNH₄ at a concentration that varies from 1 to 100 mM and a detergent at a concentration that varies from 0.01 to 1%.

23. Method as set forth in claim 22, in which the pellet is resuspended with 50 mM AcNH₄ and 0.0% Tween 20.

24. Method as set forth in claim 18, in which the bacterium G. vaginalis is grown in a broth chosen in a group consisting of Brain Hearth Infusion Broth, Cooked Meat Medium, Mueller Hinton Broth, Liver Broth, Nutrient Broth, Schaedler Anaerobe Broth, Todd-Hewitt Broth, Tryptone Soya Broth, Tryptose Phosphate Broth, Wilkins-Chalgren Anaerobe Broth, said broth being added with glycogen from 0.5 to 10% and MgSO₄ or MgCl₂ from 0.05 to 20 mM.

25. Method as set forth in claim 24, in which the broth is BHI broth comprising 0.3% glycogen and 1 mM MgSO₄ or MgCl₂.

26. Method as set forth in claim 18, in which the immune enzymatic analysis consists in an ELISA test.

27. Method as set forth in claim 26, in which the ELISA test is performed at room temperature.

28. Kit for the determination anti-Gvh IgA and/or IgG and/or IgM in a body fluid sample of women, said kit comprising the Gvh toxin isolated in accord with claim 18.

29. Kit as claimed in claim 28 for the quantitative determination of anti-Gvh IgA and/or IgG and/or IgM.

30. Kit as claimed in claim 28, comprising the Gvh toxin in an amount of 2 μ

l of the isolated toxin corresponding to 0.02-0.04 μ

g of protein, or to 100 HU₅₀ of hemolytic activity.

31. Kit as claimed in claim 28, including an ELISA plate with wells prefunctionalized with the antigen and an ELISA plate with wells not functionalized with the antigen.

32. Kit as claimed in claim 31, furthermore comprising a buffer solution to be added to the well before of the incubation with the sample of biologic fluid.

33. Kit as claimed in claim 31, furthermore comprising a negative control of biologic fluid devoid of anti-Gvh Ig.

34. Kit as claimed in claim 31, comprising a positive control of biologic fluid containing anti-Gvh Ig.

35. Kit as claimed in claim 31, furthermore comprising a concentrated solution of an anti-Ig antibody conjugated with a revealing enzyme.

36. Kit as set forth in claim 35, furthermore comprising a solution suitable to dilute a concentrated solution of antibody.

37. Kit as claimed in claim 31, furthermore comprising a substrate suitable to the quantitative detection of the enzymatic activity conjugated with the anti-Ig antibody.

38. Kit as claimed in claim 31, furthermore comprising a solution suitable to dilute a concentrated solution or a tablet of substrate.

39. Kit as claimed in claim 31, furthermore comprising an agent that stops the color development.

40. Kit as claimed in claim 31, furthermore comprising a concentrated solution for the washing of the wells before use.

41. Kit as claimed in claim 31, furthermore comprising an illustrative leaflet containing the instructions for the proper use of the kit.

42. Kit as claimed in claim 41, in which the instructions of the illustrative leaflet comprise the indication of the risk of pathologies as absent or low (−

), medium (+), high (++), very high (+++).

43. Kit as claimed in claim 31, in which the Gvh toxin is supplied in a lyophilized or frozen form.

44. Kit as claimed in claim 31, comprising a reactive strip that support the Gvh toxin.

45. Kit as claimed in claim 44, in which the Gvh toxin is supported on a piece of cellulose, or nitrocellulose, or cellulose acetate, or Dacron, or polysulfone, or PVDF, or Mylar of said strip.

46. Kit as claimed in claim 31, comprising an ELISA plate and a pH indicator with a turning range from pH 4 to pH 7.

47. Kit as claimed claim 31, comprising an ELISA plate and a test in solution for the determination of the sialidase activity.

48. Kit as claimed in claim 31, comprising an ELISA plate and a test in solution for the determination of the prolidase activity.

49. Kit as claimed in claim 31, comprising an ELISA plate and two tests in solution for the determination of the sialidase and prolidase activity, respectively.

50. Kit as claimed in claim 31, comprising an ELISA plate, a pH indicator, and a test in solution for the determination of the sialidase activity.

51. Kit as claimed in claim 31, comprising an ELISA plate, a pH indicator, and a test in solution for the determination of the prolidase activity.

52. Kit as claimed in claim 31, comprising an ELISA plate, a pH indicator, and two tests in solution for the determination of the sialidase and prolidase activity, respectively.

53. Kit as claimed in claim 31, comprising an ELISA plate, a pH indicator, and two tests on solid support for the determination of the sialidase and prolidase activity, respectively.

54. Kit as claimed in claim 53, including the reference scales for anti-Gvh Ig, pH, sialidase activity, and prolidase activity.

55. Kit as claimed in claim 28, comprising a QuickCard having a membrane functionalized with the Gvh antigen and a membrane not functionalized with the Gvh antigen as negative control.

56. Kit as claimed in claim 55, including a reference scale.

57. Kit as claimed in claim 28, comprising a QuickCard and a pH indicator on support with a sensitivity interval from pH 4 to pH 7.

58. Kit as claimed in claim 28, comprising a QuickCard and a test on solid support, preferably, platform or reactive strip, with a reference scales for the determination of the sialidase activity.

59. Kit as claimed in claim 28, comprising a QuickCard and a test on solid support, preferably, platform or reactive strip, with a reference scales for the determination of the prolidase activity.

60. Kit as claimed in claim 28, comprising a QuickCard and a test on solid support, preferably, platform or reactive strip, with a reference scales for the determination of the sialidase activity and prolidase activity.

61. Kit as claimed in claim 28, comprising a QuickCard, a pH indicator and a test on solid support, preferably, platform or reactive strip, for the determination of the sialidase activity.

62. Kit as claimed in claim 28, comprising a QuickCard, a pH indicator and a test on solid support, preferably, platform or reactive strip, for the determination of the prolidase activity.

63. Kit as claimed in claim 28, comprising a QuickCard, a pH indicator and a test on solid support, preferably, platform or reactive strip, for the determination of the sialidase activity and prolidase activity.

64. Kit as claimed in claim 28, comprising a QuickCard, a pH indicator and two tests in solution for the determination of the sialidase activity and prolidase activity, respectively.