TY - JOUR
T1 - Subclinical mastitis disrupts oocyte cytoplasmic maturation in association with reduced developmental competence and impaired gene expression in preimplantation bovine embryos
AU - Roth, Z.
AU - Asaf, S.
AU - Furman, O.
AU - Lavon, Y.
AU - Kalo, D.
AU - Wolfenson, D.
AU - Leitner, G.
N1 - Publisher Copyright:
© CSIRO 2016.
PY - 2016
Y1 - 2016
N2 - Subclinical chronic mastitis was induced to examine the effects on oocyte developmental competence. Uninfected Holstein cows were intramammary administrated with serial (every 48h for 20 days) low doses of toxin of Staphylococcus aureus origin (Gram-positive; G+), endotoxin of Escherichia coli origin (Gram-negative; G-) or sterile saline (control). Follicular fluid of toxin- and saline-treated cows was aspirated from preovulatory follicles and used as maturation medium. Oocytes harvested from ovaries collected at the abattoir were matured and then fertilised and cultured for 8 days. The percentage of oocytes undergoing nuclear maturation, determined by meiotic nuclear stages, did not differ between groups. Cytoplasmic maturation, determined by cortical granule distribution, was affected by both toxins (P<0.05). The percentage of oocytes cleaving to 2- and 4-cell embryos and of embryos developing to the blastocyst stage was lower in both toxin-treated groups than in the control group (P<0.05). There was no significant difference in the total cell number in Day 8 blastocysts among the groups; however, the apoptotic index was higher in both toxin-treated groups compared with control (P<0.05). The relative abundance of prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclo-oxygenase; PTGS2) mRNA increased, whereas that of growth differentiation factor 9 (GDF9) decreased in matured oocytes. In addition, PTGS2 expression increased and POU class 5 homeobox 1 (POU5F1) expression decreased in 4-cell embryos developed from both G+ and G- oocytes. Thus, regardless of toxin type, subclinical mastitis disrupts oocyte cytoplasmic maturation and alters gene expression in association with reduced developmental competence.
AB - Subclinical chronic mastitis was induced to examine the effects on oocyte developmental competence. Uninfected Holstein cows were intramammary administrated with serial (every 48h for 20 days) low doses of toxin of Staphylococcus aureus origin (Gram-positive; G+), endotoxin of Escherichia coli origin (Gram-negative; G-) or sterile saline (control). Follicular fluid of toxin- and saline-treated cows was aspirated from preovulatory follicles and used as maturation medium. Oocytes harvested from ovaries collected at the abattoir were matured and then fertilised and cultured for 8 days. The percentage of oocytes undergoing nuclear maturation, determined by meiotic nuclear stages, did not differ between groups. Cytoplasmic maturation, determined by cortical granule distribution, was affected by both toxins (P<0.05). The percentage of oocytes cleaving to 2- and 4-cell embryos and of embryos developing to the blastocyst stage was lower in both toxin-treated groups than in the control group (P<0.05). There was no significant difference in the total cell number in Day 8 blastocysts among the groups; however, the apoptotic index was higher in both toxin-treated groups compared with control (P<0.05). The relative abundance of prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclo-oxygenase; PTGS2) mRNA increased, whereas that of growth differentiation factor 9 (GDF9) decreased in matured oocytes. In addition, PTGS2 expression increased and POU class 5 homeobox 1 (POU5F1) expression decreased in 4-cell embryos developed from both G+ and G- oocytes. Thus, regardless of toxin type, subclinical mastitis disrupts oocyte cytoplasmic maturation and alters gene expression in association with reduced developmental competence.
KW - dairy cows
KW - fertility
KW - mammary gland
UR - http://www.scopus.com/inward/record.url?scp=84987909458&partnerID=8YFLogxK
U2 - 10.1071/RD14431
DO - 10.1071/RD14431
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AN - SCOPUS:84987909458
SN - 1031-3613
VL - 28
SP - 1653
EP - 1662
JO - Reproduction, Fertility and Development
JF - Reproduction, Fertility and Development
IS - 11
ER -