Journal of Equine Veterinary Science for the 10th International Symposium on Equine Embryo Transfer and Technology, 2020

Types of contributions

1. Contributions to the International Symposium on Equine Embryo Transfer and Technology, 2020 (10th ISEET) Supplement should take the form of either a brief (<500 words) or extended abstract (<1400 words). Every word including affiliations, author(s), references, title, figure details, acknowledgements, references, etc. counts toward the 500 or 1400 word count.

2. The decision on whether to submit a 500- or a 1400-word abstract is at the authors’ discretion. The selection of abstracts for presentation at the 10th ISEET will be based on review of the submitted abstract, this must be the version intended for inclusion in the meeting proceedings (i.e. it is not possible to submit a 1400-word abstract for review and subsequently reduce it to 500 words for publication or vice versa). Author’s should be aware that publishing a long abstract does preclude the development of that into a full paper.

3. Authors may be the first (and/or presenting) author on only one paper, but may be a co-author on several.

Preparation of abstracts

1. The extended abstract should be written in English. Authors whose native language is not English are strongly advised to have their manuscripts checked by an English-speaking colleague prior to submission. Abstracts that do not conform to standard English style, usage or grammar will be returned to the authors for modification prior to scientific review.

2. Please follow these style guidelines (an abstract example is below):

• 10-point font in Arial
• Single spaced
• Title centred and in bold
• Author(s) and organization(s) centred
• Author(s) name should be First Initial, Middle Initial and Last Name/Surname
• Presenting authors should be identified with an asterisk (*). Every word (including affiliations, author(s), references, title, figure details, acknowledgements, references, etc.) counts toward the 500 or 1400 word count.
• For authors from multiple institutions, they should be listed as follows: IG Martin1,*, CC Macedo1, GA Monteiro1, DP Leme2, FC Landim-Alvarenga1, FO Papa1 1Department of Animal Reproduction, College of Veterinary Medicine and Animal Science, Unesp, Botucatu, Brazil; 2Department of Animal Science and Rural Development, UFSC, Florianópolis, Brazil
• Fully justified, aligned text to both left and right margins
• 500 word abstracts should be one paragraph with no breaks
   o References should be minimal for the short abstracts and embedded in the text . Example: Squires et al. Animal Reproduction. 2005; 58:211-213
   o Acknowledgements can be a new paragraph/break.
   o Figures and Tables should be embedded in the abstract
• 1400 word abstracts should follow the guidelines for papers in the journal of Equine Veterinary Science and have numbered headings such as introduction, materials and methods, results, discussion and references. For the complete and most recent author instructions, including all details regarding ethical guidelines, author rights, nomenclature and units, reference and footnote style see: JEVS guidelines

3. Abstract example:

Immunohistochemical localization of Early Pregnancy Factor (Hsp10) in equine embryos
JN Hatzel, PM McCue, EJ Ehrhart, JB Charles, RA Ferris
Colorado State University, Equine Reproduction Laboratory, Fort Collins, CO 80521

Early Pregnancy Factor (EPF) has been identified as a 10 kDa extracellular homolog of heat shock protein 10 (Hsp10). Hsp10 has been detected during early pregnancy in serum of mice, sheep, pigs, horses, cows, and humans by the rosette inhibition test. Hsp10 has also been associated with several neoplastic and autoimmune diseases. The goal of the present study was to determine if Hsp10 could be detected in the early equine embryo by immunohistochemistry. Embryos were collected from Quarter Horse mares by uterine lavage at either 8 or 25 days after ovulation. Embryos were fixed in 10% formalin solution and embedded in paraffin. Standard H&E sections were prepared along with sections for immunohistochemical (IHC) colormetric and fluorescent staining for Hsp10. Briefly, 5 mm sections of embryos, ovarian, oviductal, and uterine tissue were mounted on positively charged slides. The sections were deparaffinized and rehydrated with descending alcohol concentrations to buffer. Heat-induced epitope retrieval with citrate buffer (pH 6.0) at 125°C for 1 minute was followed by endogenous peroxidase blocking with 3% hydrogen peroxide and incubation with the primary antibody at 4°C overnight. The primary antibody was a polyclonal rabbit anti-human Hsp10 at a 1:1000 dilution. A predilute polymer based dual link HRP conjugated secondary antibody system was applied for 30 minutes (colormetric) followed by application of a DAB substrate or Texas Red for 1 hour with a mounting substrate containing DAPI, to detect the immunoreactive complexes. The colormetric slides were subsequently counterstained with Mayer’s hematoxylin QS, dehydrated and mounted in xylene based medium. A total of 6 day eight and 4 day twenty-five embryos were collected for IHC evaluation. Day 8 embryos exhibited cytoplasmic localization of staining throughout the single layer of ectodermal cells forming the trophoblast. There was no nuclear localization. Day 25 embryos demonstrated intense localization focally along the apical boarder of the ectodermal cells forming trophoblast layer of the developing chorion (Figure 1). Evaluation of other reproductive tissues revealed staining in granulosa and luteal cells of the ovary and variable staining in the oviductal epithelium. In summary, immunolocalization of Hsp10 in trophoblast cells of the extraembryonic membranes of the early equine conceptus confirms the presence and site of protein synthesis. We hypothesize that the secretion of Hsp10 by the developing embryo could have an immunomodulatory effect on the endometrium of the mare, effectively protecting the embryo from the maternal immune system. Other tissues in the reproductive tract also exhibited evidence of Hsp10. Finally, as it is unlikely that a 150 to 300 µm morula or blastocyst stage embryo could produce sufficient Hsp10 to be detected in peripheral blood, we hypothesize that other tissues may contribute to Hsp10 production during early pregnancy. Figure 1. Day 25 trophoblast extraembryonic membrane stained with H&E (left), IHC staining for Hsp10 (center), and fluorescent (right) at 40x.


1. Please note: The regular, online method of submitting to the Journal of Equine Veterinary Science should NOT be used for papers for this supplement.
2. The platform for abstract submission will be indicated when open.
3. Abstract should be submitted before February 1st, 2020.