michael John d'occhio

Prof. michael John d'occhio

School of Life and Environmental Sciences, Faculty of Science, The University of Sydney, Sydney, NSW 2000, Australia
orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

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

Representative Publications

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1 May 2021 in Food Chemistry
Verified
Journal Article
Closed access
ASAngela Salzano
Angela Salzano
Gianluca NegliaGianluca Neglia
Gianluca Neglia
Nunzia D'OnofrioNunzia D'Onofrio
Nunzia D'Onofrio
Maria  Luisa BalestrieriMaria Luisa Balestrieri
Maria Luisa Balestrieri
ALAntonio Limone
Antonio Limone
Giuseppe CampanileGiuseppe Campanile
Giuseppe Campanile


16 January 2020 in Molecular Reproduction and Development
Verified
Journal Article
Open access
PDF file
MDmichael John d'occhio
michael John d'occhio
GCGiuseppe Campanile
Giuseppe Campanile
LZLuigi Zicarelli
Luigi Zicarelli
JVJosé A. Visintin
José A. Visintin
PBPietro Baruselli
Pietro Baruselli
Cell–cell adhesion molecules have critically important roles in the early events of reproduction including gamete transport, sperm–oocyte interaction, embryonic development, and implantation. Major adhesion molecules involved in reproduction include cadherins, integrins, and disintegrin and metalloprotease domain‐containing (ADAM) proteins. ADAMs on the surface of sperm adhere to integrins on the oocyte in the initial stages of sperm–oocyte interaction and fusion. Cadherins act in early embryos to organize the inner cell mass and trophectoderm. The trophoblast and uterine endometrial epithelium variously express cadherins, integrins, trophinin, and selectin, which achieve apposition and attachment between the elongating conceptus and uterine epithelium before implantation. An overview of the major cell–cell adhesion molecules is presented and this is followed by examples of how adhesion molecules help shape early reproductive events. The argument is made that a deeper understanding of adhesion molecules and reproduction will inform new strategies that improve embryo survival and increase the efficiency of natural mating and assisted breeding in cattle.

12 January 2020 in Molecules
Verified
Journal Article
Open access
PDF file
ASAngela Salzano
Angela Salzano
GMGelsomina Manganiello
Gelsomina Manganiello
Gianluca NegliaGianluca Neglia
Gianluca Neglia
Francesco VinaleFrancesco Vinale
Francesco Vinale
DNDonato De Nicola
Donato De Nicola
Giuseppe CampanileGiuseppe Campanile
Giuseppe Campanile
The aim of this study is to combine advanced GC-MS and metabolite identification in a robust and repeatable technology platform to characterize the metabolome of buffalo milk and mozzarella cheese. The study utilized eleven dairies located in a protected designation of origin (PDO) region and nine dairies located in non-PDO region in Italy. Samples of raw milk (100 mL) and mozzarella cheese (100 g) were obtained from each dairy. A total of 185 metabolites were consistently detected in both milk and mozzarella cheese. The PLS-DA score plots clearly differentiated PDO and non-PDO milk and mozzarella samples. For milk samples, it was possible to divide metabolites into two classes according to region: those with lower concentrations in PDO samples (galactopyranoside, hydroxybuthyric acid, allose, citric acid) and those with lower concentrations in non-PDO samples (talopyranose, pantothenic acid, mannobiose, etc.,). The same was observed for mozzarella samples with the proportion of some metabolites (talopyranose, 2, 3-dihydroxypropyl icosanoate, etc.,) higher in PDO samples while others (tagatose, lactic acid dimer, ribitol, etc.,) higher in non-PDO samples. The findings establish the utility of GC-MS together with mass spectral libraries as a powerful technology platform to determine the authenticity, and create market protection, for “Mozzarella di Bufala Campana.”

1 May 2014 in Animal Reproduction Science
Verified
Journal Article
Closed access
FSFirooz Samadi
Firooz Samadi
DBDominique Blache
Dominique Blache
GMGraeme Bruce Martin
Graeme Bruce Martin
MDmichael John d'occhio
michael John d'occhio

15 July 2021 in Pharmaceutics
Verified
Journal Article
Open access
PDF file
MFMohammad O. Faruck
Mohammad O. Faruck
Prashamsa KoiralaPrashamsa Koirala
Prashamsa Koirala
JYJieru Yang
Jieru Yang
MDmichael John d'occhio
michael John d'occhio
Mariusz SkwarczynskiMariusz Skwarczynski
Mariusz Skwarczynski
Istvan TothIstvan Toth
Istvan Toth
Contraceptive vaccines are designed to elicit immune responses against major components of animal reproductive systems. These vaccines, which are most commonly administered via injection, typically target gonadotropin-releasing hormone (GnRH). However, the need to restrain animals for treatment limits the field applications of injectable vaccines. Oral administration would broaden vaccine applicability. We explored contraceptive vaccine candidates composed of GnRH peptide hormone, universal T helper PADRE (P), and a poly(methylacrylate) (PMA)-based delivery system. When self-assembled into nanoparticles, PMA-P-GnRH induced the production of high IgG titers after subcutaneous and oral administration in mice. PADRE was then replaced with pig T helper derived from the swine flu virus, and the vaccine was tested in pigs. High levels of systemic antibodies were produced in pigs after both injection and oral administration of the vaccine. In conclusion, we developed a simple peptide–polymer conjugate that shows promise as an effective, adjuvant-free, oral GnRH-based contraceptive vaccine.