Zygote

Research Article

Detrimental effects of antibiotics on mouse embryos in chromatin integrity, apoptosis and expression of zygotically activated genes*

Jun Liua2, Shuang Tanga2, Wei Xua2, Yongsheng Wanga2, Baoying Yina2 and Yong Zhanga1a2 c1

a1 Institute of Biotechnology, Northwest A&F University, Yangling, Shaanxi 712100, P. R. China.

a2 Key Laboratory of Animal Reproductive Physiology & Embryo Technology of the Ministry of Agriculture, College of Veterinary Medicine, Northwest A&F University, Yangling, Shaanxi 712100, China.

Summary

The effects of specific components in culture medium on embryo physiology have been extensively investigated to optimize in vitro culture systems; however, little attention has been paid to antibiotics, the reagents used most commonly in culture systems to prevent contamination. To investigate the potential effects of routine use of antibiotics on cultured embryos, mouse zygotes were cultured with or without antibiotics. In both groups, the developmental rate and cell number of blastocysts appear to be normal. The proportion of embryos with blastomere fragmentation increased slightly when embryos were cultured with antibiotics. In contrast, the presence of antibiotics in the embryo culture system significantly disturbs expression of zygotically activated genes, damages chromatin integrity and increases apoptosis of cultured embryos. These results provide evidence that, when cultured with antibiotics, embryos with normal appearance may possess intrinsic physiological and genetic abnormalities. We demonstrate that the adverse effects of antibiotics on mammalian embryos are more severe than we previously presumed and that antibiotics are not essential for sterility of embryo culture system therefore abolishing antibiotic supplementation during embryo culture.

(Received October 19 2009)

(Accepted March 19 2010)

(Online publication June 30 2010)

Correspondence:

c1 All correspondence to: Yong Zhang. Institute of Biotechnology, Northwest A&F University, Yangling, Shaanxi 712100, P. R. China. Fax: +86 02987080085. e-mail: zhangylab@yahoo.com.cn

* This work is supported by grants from the Important National Science & Technology Specific Projects, China (No. 2008ZX08007-004).

† These two authors contributed equally to this work.

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