Warning: mkdir(): Permission denied in /home/virtual/lib/view_data.php on line 81

Warning: fopen(upload/ip_log/ip_log_2024-11.txt): failed to open stream: No such file or directory in /home/virtual/lib/view_data.php on line 83

Warning: fwrite() expects parameter 1 to be resource, boolean given in /home/virtual/lib/view_data.php on line 84
An experimental study on the pathogenicity of Korean strains of Trichomonas vaginalis
| Home | E-Submission | Sitemap | Contact us |  
top_img
Korean J Parasito Search

CLOSE

Korean J Parasito > Volume 17(1):1979 > Article

Original Article
Korean J Parasitol. 1979 Jun;17(1):1-9. English.
Published online Mar 20, 1994.  http://dx.doi.org/10.3347/kjp.1979.17.1.1
Copyright © 1979 by The Korean Society for Parasitology
An experimental study on the pathogenicity of Korean strains of Trichomonas vaginalis
Hi Chu Song,Soon Hyung Lee and Je G. Chi
Department of Urology and Department of Parasitology, College of Medicine, Chung-Ang University, Korea.
Department of Pathology, College of Medicine, Seoul National University, Korea.
Abstract

In order to evaluate the pathogenicity of Korean strains of Trichomonas vaginalis, an experimental inoculation of T. vaginalis into mouse peritoneal cavity was performed.

Fifteen strains of T. vaginalis were selected from 53 infected cases and were cultured axenically in Roiron-Rattner medium at 37℃ for 48 hours. Each strain, at the dose of 0.5 ml of 1×106/ml trichomonads, was inoculated intraperitoneally to a group of 10 mice, respectively.

A total of 15 groups, consisted of 150 mice, were sacrificed on the 8th day of inoculation, and then they were thoroughly examined for the detection of the lesion.

The results obtained in present study were summarized as follows:

1. Prior to inoculation, the positive rates in 2 kinds of media cultivating T. vaginalis were compared. In Johnson's CPLM medium, 65% of positive rate was obtained, and 94.2% of positive rate, the better result, was shown in the culture of Roiron-Rattner medium.

2. Overall death rate of 150 inoculated mice was 7.3% (range 0~40%), and 7 strains (46.7%) out of 15 inoculated strains were proved as fatal strain.

3. The intraperitoneal lesions produced by the inoculation of T. vaginalis were observed in the liver (20%), intestinal wall and mesentery (14%), peritoneal wall (9.3%), wall of the stomach (6.0%), and the spleen (5.3%) of 150 inoculated mice. Occasionally, the lesions were also found in the pancreas and wall of the urinary bladder.

In 11.3% of inoculated mice, purulent ascites with living trichomonads could be seen.

Thirteen strains (86.7%) out of the 15 inoculated strains produced the T. vaginalis-associated pathological lesions.

4. On the histopathological investigation of those lesions, intraperitoneal inoculation was characterzed by a necrotizing granulomatous inflammation, i.e., acutely necrotizing process with areas of encircling granuloma formation.

Numerous free lying trichomonads were seen along the expanding margin of the lesion. Where there were free trichomonads, the reaction was usually of necrotizing. And these organisms directly eroded the vascular wall and often provoked thrombosis.

From the above findings, it is considered that the Korean strains of T. vaginalis are highly pathogenic.

Figures


EXPLANATION OF THE PLATES
Fig. 1. Clusters of Trichomonas vaginalis in culture medium. (Unstained, ×100)

Fig. 2. A smear of the ascitic fluid derived from intraperitioneal inoculation of T. vaginalis into mice.The organisms are distinct among the inflammatory cells. (Giemsa stain, ×200)

Fig. 3. The liver is covered with large caseous and fibropurulent masses.

Fig. 4. Adhesion of the stomach, spleen, pancreas and peritoneal wall occurred dut to large caseous mass.

Fig. 5. Photomicrograph of hepatic lesion shows necrotizing area of nodular granuloma and histiolymphocytic infiltration. (H-E stain, ×200)

Fig. 6. Higher magnification of Fig. 5. Free trichomonads are seen along the expanding margin of the lesion. Large mononuclear cells (histiocytes) are prominent among the infiltrated inflammatory cells. (H-E stain, ×400)


Tables


Table 1
Contents of Johnson's CPLM medium


Table 2
Contents of medium after Roiron-Rattner (1957/8)


Table 3
Comparison of media for cultivation of Trichomonas vaginalis


Table 4
The death rate due to intraperitoneal inoculation of Trichomonas vaginalis in the mouse (period of observation: 7 days)


Table 5
Number of mice died due to intraperitoneal inoculation of Trichomonas vaginalis by days


Table 6
Pathological changes produced by the intraperitoneal inoculation of Trichomonas vaginalis in the mouse (Period of observation: 7 days)

References
1. Feo LG. Am J Trop Med 1944;24:195–198.
2. Frost JK, Honigberg BM. Comparative pathogenicity of Trichomonas vaginalis and Trichomonas gallinae to mice. II. Histopathology of subcutaneous lesions. J Parasitol 1962;48:898–918.
  
3. Frost JK, et al. J Parasitol 1961;47:302–303.
 
4. Hamada Y. Jpn J Parasit 1956;5(3):365–369.
5. Honigbers BM. J Parasit 1959;45 Suppl:51.
6. Honigberg BM. Comparative pathogenicity of Trichomonas vaginalis and Trichomonas gallinae to mice. I. Gross pathology, quantitative evaluation of virulence, and some factors affecting pathogenicity. J Parasitol 1961;47:545–571.
  
7. Inoki S. Jpn J Parasit 1958;7(3):310–311.
8. Inoki S, Hamada Y. Experimental transmission of Trichomonas vaginalis (pure culture) into mice. J Infect Dis 1953;92(1):1–3.
  
9. Ivey MH, Hall DG. Virulence of Different Strains of Trichomonas Vaginalis in the Mouse. Am J Trop Med Hyg 1964;13:16–19.
 
10. Iwai S. Jpn J Parasit 1957;6(2):144–156.
11. Kim YC. Korean J Ob & Gyn 1962;5(4):41–46.
12. Nakabayashi T, et al. Jpn J Parasit 1962;11:150–156.
13. Newton WL, Reardon LV, Deleva AM. A comparative study of the subcutaneous inoculation of germfree and conventional guinea pigs with two strains of Trichomonas vaginalis. Am J Trop Med Hyg 1960;9:56–61.
 
14. Reardon LV, et al. J Parasit 1958;44 Suppl:21.
15. Reardon LV, Ashburn LL, Jacobs L. Differences in strains of Trichomonas vaginalis as revealed by intraperitoneal injections into mice. J Parasitol 1961;47:527–532.
  
16. Schnitzer RJ, Kelly DR, Leiwant B. Experimental studies on trichomoniasis: 1. The pathogenicity of trichomonad species for mice. J Parasitol 1950;36(4):343–349.
  
Editorial Office
Department of Molecular Parasitology, Samsung Medical Center, School of Medicine, Sungkyunkwan University,
2066 Seobu-ro, Jangan-gu, Suwon 16419, Gyeonggi-do, Korea.
Tel: +82-31-299-6251   FAX: +82-1-299-6269   E-mail: kjp.editor@gmail.com
About |  Browse Articles |  Current Issue |  For Authors and Reviewers
Copyright © 2024 by The Korean Society for Parasitology and Tropical Medicine.     Developed in M2PI