Jessica Paige Rickard

Dr. Jessica Paige Rickard

School of Life and Environmental Sciences, The University of Sydney, New South Wales 2006, Australia
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2013 in Journal of Proteomics
Verified
Journal Article
Closed access
XDX. Druart
X. Druart
Jessica Paige RickardJessica Paige Rickard
Jessica Paige Rickard
SMS. Mactier
S. Mactier
PKP.L. Kohnke
P.L. Kohnke
CKC.M. Kershaw-Young
C.M. Kershaw-Young
Simon De GraafSimon De Graaf
Simon De Graaf

1 August 2015 in Journal of Proteomics
Verified
Journal Article
Closed access
Jessica Paige RickardJessica Paige Rickard
Jessica Paige Rickard
TLTamara Leahy
Tamara Leahy
CSC. Soleilhavoup
C. Soleilhavoup
GTG. Tsikis
G. Tsikis
VLV. Labas
V. Labas
Simon De GraafSimon De Graaf
Simon De Graaf

1 June 2018 in Journal of Proteomics
Verified
Journal Article
Closed access
TPTaylor Pini
Taylor Pini
Jessica Paige RickardJessica Paige Rickard
Jessica Paige Rickard
TLT. Leahy
T. Leahy
BCB. Crossett
B. Crossett
XDX. Druart
X. Druart
Simon De GraafSimon De Graaf
Simon De Graaf

26 September 2016 in Journal of Proteome Research
Verified
Journal Article
Closed access
TPTaylor Pini
Taylor Pini
TLTamara Leahy
Tamara Leahy
CSClement Soleilhavoup
Clement Soleilhavoup
GTGuillaume Tsikis
Guillaume Tsikis
VLValerie Labas
Valerie Labas
Simon De GraafSimon De Graaf
Simon De Graaf

26 November 2022 in Biology
Verified
Journal Article
Open access
PDF file
MHMadeleine Van de Hoek
Madeleine Van de Hoek
Jessica Paige RickardJessica Paige Rickard
Jessica Paige Rickard
Simon De GraafSimon De Graaf
Simon De Graaf
For successful fertilisation to occur, spermatozoa need to successfully migrate through the female reproductive tract and penetrate the oocyte. Predictably, poor sperm motility has been associated with low rates of fertilisation in many mammalian species, including the ram. As such, motility is one of the most important parameters used for in vitro evaluation of ram sperm quality and function. This review aims to outline the mechanical and energetic processes which underpin sperm motility, describe changes in motility which occur as a result of differences in sperm structure and the surrounding microenvironment, and assess the effectiveness of the various methods used to assess sperm motility in rams. Methods of subjective motility estimation are convenient, inexpensive methods widely used in the livestock industries, however, the subjective nature of these methods can make them unreliable. Computer-assisted sperm analysis (CASA) technology accurately and objectively measures sperm motility via two-dimensional tracing of sperm head motion, making it a popular method for sperm quality assurance in domesticated animal production laboratories. Newly developed methods of motility assessment including flagellar tracing, three-dimensional sperm tracing, in vivo motility assessment, and molecular assays which quantify motility-associated biomarkers, enable analysis of a new range of sperm motion parameters with the potential to reveal new mechanistic insights and improve ram semen assessment. Experimental application of these technologies is required to fully understand their potential to improve semen quality assessment and prediction of reproductive success in ovine artificial breeding programs.

1 November 2014 in Reproduction
Verified
Journal Article
Closed access
Jessica Paige RickardJessica Paige Rickard
Jessica Paige Rickard
TPTaylor Pini
Taylor Pini
CSC Soleilhavoup
C Soleilhavoup
JCJ Cognie
J Cognie
RBRoslyn Bathgate
Roslyn Bathgate
Simon De GraafSimon De Graaf
Simon De Graaf
Seminal plasma purportedly plays a critical role in reproduction, but epididymal spermatozoa are capable of fertilisation following deposition in the uterus, calling into question the biological requirement of this substance. Through a combination of direct observation of spermatozoa in utero using probe-based Confocal Laser Endomicroscopy, in vivo assessment of sperm fertility and in vitro analysis of various sperm functional parameters, this study investigated the role of seminal plasma in spermatozoa transit through the cervix of the ewe. Following deposition in the cervical os, epididymal spermatozoa previously exposed to seminal plasma displayed an enhanced ability to traverse the cervix as evidenced by both significantly higher pregnancy rates and numbers of spermatozoa observed at the utero-tubal junction when compared with epididymal spermatozoa not previously exposed to seminal plasma. The beneficial effect of seminal plasma on sperm transport was clearly localised to transit through the cervix as pregnancy rates of spermatozoa deposited directly into the uterus were unaffected by exposure to seminal plasma. This phenomenon was not explained by changes to sperm motion characteristics, as seminal plasma had no effect on the motility, kinematic parameters or mitochondrial membrane potential of spermatozoa. Rather, in vitro testing revealed that seminal plasma improved the ability of epididymal spermatozoa to penetrate cervical mucus recovered from ewes in oestrus. These results demonstrate that the survival and transport of ram spermatozoa through the cervix of the ewe is not linked to their motility or velocity but rather the presence of some cervical penetration trait conferred by exposure to seminal plasma.