Antibiotic Resistant Microbial Contamination (Enterobacter cloacae) Derived from Egg Yolk and Frozen Semen Extender in Porcine In Vitro Fertilized Embryos

  • Kwak, Seong-Song (Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University) ;
  • Jeong, Se-Heon (Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University) ;
  • Jang, Seung-Hoon (Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University) ;
  • Jeon, Yu-Byeol (Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University) ;
  • Nam, Young-Hee (Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University) ;
  • Biswas, Dibyendu (Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University) ;
  • Lee, Wan-Kyu (Laboratory of Veterinary Bacteriology, College of Veterinary Medicine, Chungbuk National University) ;
  • Hyun, Sang-Hwan (Laboratory of Veterinary Embryology and Biotechnology (VETEMBIO), College of Veterinary Medicine, Chungbuk National University)
  • Received : 2010.11.18
  • Accepted : 2010.11.30
  • Published : 2010.12.31

Abstract

The present study was to investigate the source of contamination during semen processing for in vitro uses. In the present study, frozen semen was prepared from liquid semen in our laboratory for in vitro fertilization (IVF) experiments due to lack of fresh semen. Antibiotics were added in the frozen semen extender (kanamycin and gentamicin) and in vitro culture (IVC) medium (gentamicin) for further inhibiting growth of microorganisms. Nevertheless, proliferations of microorganisms were observed in IVC culture drop during culturing of IVF embryos using frozen semen. Randomly 3 samples were taken from the liquid semen, frozen semen and egg yolk. Contaminated IVC medium, frozen-thawed semen, liquid semen and egg yolk were cultured in de Man, Rogosa and Sharpe (MRS) agar medium. Whitish colonies were detected in contaminated IVC drop, frozen-thawed semen samples and egg yolk but no colonies were formed in liquid semen samples. Gram-negative and rod-shaped identical bacteria were found in both frozen-thawed semen sample and contaminated IVC drop and egg yolk samples. Enterobacter cloacae were confirmed by API 20E kit according to manufacturer's instruction with identification value (% ID) 94.3% and T index 0.88. Antibiotic susceptibility tests were done according to Clinical and Laboratory Standards Institute (CLSI) by using ampicillin, amikacin, cephalothin, gentamicin, kanamycin, tetracycline, oxytetracycline, sulfamethoxazole trimethoprim, norfloxacin and ciprofloxacin test. Among them Enterobacter cloacae were resistant to ampicillin, amikacin, cephalothin, gentamicin, kanamycin but susceptible to tetracycline, oxytetracycline, sulfamethoxazole trimethoprim, norfloxacin and ciprofloxacin. From these findings it could be suggested that this contamination sources might be from egg yolk.

Keywords

References

  1. Abeydeera L and Day B. 1997. In vitro penetration of pig oocytes in a modified Tris-buffered medium: effect of BSA, caffeine and calcium. Theriogenology 48:537-544. https://doi.org/10.1016/S0093-691X(97)00270-7
  2. Afshar A and Eaglesome M. 1990. Viruses associated with bovine semen. Veterinary Bulletin (United Kingdom) 60:93-109.
  3. Aldridge K, Gardner B, Clark S and Matsen J. 1978. Comparison of Micro-ID, API 20E, and conventional media systems in identification of Enterobacteriaceae. J. Clin. Microbiol. 7:507-513.
  4. Bagg M, Vassena R, Papasso-Brambilla E, Grupen C, Armstrong D and Gandolfi F. 2004. Changes in ovarian, follicular, and oocyte morphology immediately after the onset of puberty are not accompanied by an increase in oocyte developmental competence in the pig. Theriogenology 62:1003-1011. https://doi.org/10.1016/j.theriogenology.2003.12.028
  5. Bavister B, Leibfried M and Lieberman G. 1983. Development of preimplantation embryos of the Golden Hamster in a defined culture medium. Biol. Reprod. 28:235-247. https://doi.org/10.1095/biolreprod28.1.235
  6. Benson RW, Pickett BW, Komarek RJ and Lucas JJ. 1967. Effect of incubation and cold shock on motility of boar spermatozoa and their relationship to lipid content. J. Anim. Sci. 26:1078-1081.
  7. Bielanski A and Vajta G. 2009. Risk of contamination of germplasm during cryopreservation and cryobanking in IVF units. Hum. Reprod. 24:2457-2467. https://doi.org/10.1093/humrep/dep117
  8. Bielanski A. 2007. Disinfection procedures for controlling microorganisms in the semen and embryos of humans and farm animals. Theriogenology 68:1-22. https://doi.org/10.1016/j.theriogenology.2007.03.025
  9. Bousseau S, Brillard JP, Marquant-Leguienne B, Guerin B, Camus A and Lechat M. 1998. Comparison of bacteriological qualities of various egg yolk sources and the in vitro and in vivo fertilizing potential of bovine semen frozen in egg yolk or lecithin based diluents. Theriogenology 50:699-706. https://doi.org/10.1016/S0093-691X(98)00175-7
  10. Cottell E, McMorrow J, Lennon B, Fawsy M, Cafferkey M and Harrison R. 1996. Microbial contamination in an in vitro fertilization-embryo transfer system. Fertility and sterility 66:776-780.
  11. De Man J, Rogosa M and Sharpe M. 1960. A medium for the cultivation of lactobacilli. J. Appl. Microbiol. 23:130-135. https://doi.org/10.1111/j.1365-2672.1960.tb00188.x
  12. Dejucq-Rainsford Nand Jegou B. 2004. Viruses in semen and male genital tissues-consequences for the reproductive system and therapeutic perspectives. Curro Pharm. Des. 10:557-575. https://doi.org/10.2174/1381612043453225
  13. Eaglesome M and Garcia M. 1992. Microbial agents associated with bovine genital tract infections and semen. Part I. Brucella abortus, Leptospira, Campylobacter fetus and Tritrichomonas foetus. Veterinary Bulletin, United Kingdom.
  14. Eaglesome M, Garcia M and Stewart R. 1992. Microbial agents associated with bovine genital tract infections and semen. Part II. Haemophilus somnus, Mycoplasma spp. and Ureaplasma spp., Chlamydia; pathogens and semen contaminants; treatments of bull semen with antimicrobial agents. Veterinary Bulletin, United Kingdom.
  15. Graham EF, Rajamannan AHJ, Schmehl MKL, Maki-Laurila M and Bower RE. 1971. Preliminary report on procedure and rationale for freezing boar semen. A.I. Digest 19:12.
  16. Hare WCD. 1985. Diseases transmissible by semen and embryo transfer technigues. OIE Technical. Bull. 4:1-117.
  17. Johnson L, Weitze K, Fiser P and Maxwell W. 2000. Storage of boar semen. Anim. Reprod. Sci. 62:143-172. https://doi.org/10.1016/S0378-4320(00)00157-3
  18. Kastrop PM, de Graaf-Miltenburg LA, Gutknecht DR and Weima SM. 2007. Microbial contamination of embryo cultures in an ART laboratory: sources and management. Hum. Reprod. 22:2243-2248. https://doi.org/10.1093/humrep/dem165
  19. Kim H, Lee G, Hyun S, Lee S, Nam D, Jeong Y, Kim S, Kang S, Lee B and Hwang W. 2004. Improved in vitro development of porcine embryos with different energy substrates and serum. Theriogenology 61:1381-1393. https://doi.org/10.1016/j.theriogenology.2003.08.012
  20. Papadopoulou C, Dimitriou D, Levidiotou S, Gessouli H, Panagiou A, Golegou S and Antoniades G. 1997. Bacterial strains isolated from eggs and their resistance to currently used antibiotics: Is there a health hazard for consumers? Comp. Immunol. Microbial. Infect. Dis. 20:35-40. https://doi.org/10.1016/S0147-9571(96)00024-0
  21. Pursel V and Johnson L. 1975. Freezing of boar spermatozoa: fertilizing capacity with concentrated semen and a new thawing procedure. J. Anim. Sci. 40:99-102.
  22. Pursel V, Schulman L and Jolmson L. 1978. Effect of Orvus ES Paste on acrosome morphology, motility and fertilizing capacity of frozen-thawed boar sperm. J. Anim. Sci. 47:198-202.
  23. Richter C, Romeny E, Weitze K and Zimmermann F. 1975. Deep freezing of boar semen VII communication: laboratory and field experiments using the extender Hulsenberg VIII. Dtsch. Tierarztl. Wschr. 82:155-162.
  24. Sanders WE Jr and Sanders CC. 1997. Enterobacter spp.: Pathogens poised to flourish at the turn of the century. Clin. Microbiol. Rev. 10:220-241.
  25. Sellers RF. 1983. Transmission of viruses by artificial breeding techniques: a review. J. R. Soc. Med. 76:772-775.
  26. Suzuki M, Misumi K, Ozawa M, Noguchi J, Kaneko H, Olmuma K, Fuchimoto D, Onishi A, Iwamoto M and Saito N. 2006. Successful piglet production by IVF of oocytes matured in vitro using NCSU-37 supplemented with fetal bovine serum. Theriogenology 65:374-386. https://doi.org/10.1016/j.theriogenology.2005.05.039
  27. Tong G, Heng B, Chen N, Yip W and Ng S. 2004. Effects of elevated temperature in vivo on the maturational and developmental competence of porcine germinal vesicle stage oocytes. J. Anim. Sci. 82:3175-3180.
  28. Wang W, Niwa K and Okuda K. 1991. In-vitro penetration of pig oocytes matured in culture by frozen-thawed ejaculated spermatozoa. J. Reprod. Fertil. 93:491-496. https://doi.org/10.1530/jrf.0.0930491
  29. Yoshioka K, Suzuki C, Tanaka A, Anas I and Iwamura S. 2002. Birth of piglets derived from porcine zygotes cultured in a chemically defined medium. Biol. Reprod. 66:112-129. https://doi.org/10.1095/biolreprod66.1.112