Abstract: Septic arthritis is considered a medical emergency. Disease following bacterial colonization can lead to significant morbidity and mortality and requires costly treatment. Antimicrobial properties of regenerative therapies, including mesenchymal stromal cells and platelet products, have been researched extensively in human medicine. Although fewer studies have been conducted in veterinary species, they have shown promising results. The purpose of this study was to evaluate bacterial suppression by equine platelet lysate (EPL) and adipose-derived mesenchymal stromal cells (ASCs) in vitro. We hypothesized that both products would significantly inhibit the growth of Staphylococcus aureus and Escherichia coli. Pooled blood from 10 horses was used for production of EPL. Mesenchymal stromal cells were isolated from adipose tissue harvested from the gluteal region of 3 horses. The study evaluated 3 treatment groups: 10 × EPL, 1.6 million ASCs, and a control, using an incomplete unbalanced block design with repeated measurements. Optical density readings and colony-forming units/mL were calculated at 0, 3, 6, 9, 12, 18, and 24 hours. Decreased bacterial growth was seen at multiple time points for the S. aureus-ASC and S. aureus-EPL treatments, supporting our hypothesis. Increased bacterial growth was noticed in the E. coli-EPL group, with no difference in the E. coli-ASC treatment, which opposed our hypothesis. A clear conclusion of antimicrobial effects of EPL and ASCs cannot be made from this in vitro study. Although it appears that ASCs have a significant effect on decreasing the growth of S. aureus, further studies are needed to explore these effects, particularly in Gram-positive bacteria. L’arthrite septique est considérée comme une urgence médicale. La maladie consécutive à une colonisation bactérienne peut entraîner une morbidité et une mortalité importantes et nécessite un traitement coûteux. Les propriétés antimicrobiennes des thérapies régénératives, y compris les cellules stromales mésenchymateuses et les produits plaquettaires, ont fait l’objet de recherches approfondies en médecine humaine. Bien que moins d’études aient été menées chez les espèces animales, elles ont montré des résultats prometteurs. Le but de cette étude était d’évaluer la suppression bactérienne par le lysat plaquettaire équin (EPL) et les cellules stromales mésenchymateuses adipeuses (ASC) i n vitro. Nous avons émis l’hypothèse que les deux produits inhiberaient de manière significative la croissance de Staphylococcus aureus et d’Escherichia coli. Un pool de sang de 10 chevaux a été utilisé pour la production d’EPL. Des cellules stromales mésenchymateuses ont été isolées à partir de tissu adipeux prélevé dans la région fessière de trois chevaux. L’étude a évalué trois groupes de traitement : 10 × EPL, 1,6 million d’ASC et un témoin, en utilisant un design en blocs non équilibrés incomplets avec des mesures répétées. Les lectures de densité optique et les unités formatrices de colonie/mL ont été calculées à 0, 3, 6, 9, 12, 18 et 24 heures. Une diminution de la croissance bactérienne a été observée à plusieurs moments pour les traitements S. aureus-ASC et S. aureus-EPL, soutenant notre hypothèse. Une croissance bactérienne accrue a été remarquée dans le groupe E. coli-EPL, sans différence dans le traitement E. coli-ASC, ce qui s’opposait à notre hypothèse. Une conclusion claire des effets antimicrobiens de l’EPL et des ASC ne peut pas être tirée de cette étude in vitro. Bien qu’il semble que les ASC aient un effet significatif sur la diminution de la croissance de S. aureus, d’autres études sont nécessaires pour explorer ces effets, en particulier chez les bactéries à Gram positif.(Traduit par Docteur Serge Messier).
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This research study explores the potential of equine platelet lysate and adipose-derived mesenchymal stromal cells in inhibiting bacterial growth, focusing on Staphylococcus aureus and Escherichia coli. The results partially support the hypothesis, with significant bacterial suppression observed against S. aureus but not E. coli. Further studies are needed to fully understand the antimicrobial effects of these substances.
Study Objective and Hypothesis
The primary aim of the research was to investigate the bacterial suppression properties of equine platelet lysate (EPL) and adipose-derived mesenchymal stromal cells (ASCs).
The study hypothesized that both EPL and ASCs would significantly inhibit the growth of two common bacteria: Staphylococcus aureus and Escherichia coli.
Research Methodology
Blood from 10 horses was pooled to produce EPL, while ASCs were isolated from adipose tissue from the gluteal region of 3 horses.
Three treatment groups were created: one with a 10-fold concentration of EPL, the second with 1.6 million ASCs, and a control group.
An incomplete unbalanced block design with repeated measurements was used in the experiment.
Optical density readings and colony-forming units/mL were recorded at multiple intervals: 0, 3, 6, 9, 12, 18, and 24 hours.
Study Outcomes
Evidence of decreased bacterial growth was seen at multiple time points for the S. aureus-ASC and S. aureus-EPL treatments, supporting the research hypothesis.
In contrast, increased bacterial growth was noticed in the E. coli-EPL group, contradicting the hypothesis. There was no change observed in the E. coli-ASC treatment, also challenging the study’s prediction.
Conclusions and Further Study
No definitive conclusion on the antimicrobial effects of EPL and ASCs could be drawn from this in vitro study.
Although the research suggests that ASCs have a significant effect on reducing S. aureus growth, additional studies are necessary to validate and further explore these effects, particularly concerning Gram-positive bacteria such as S. aureus.
Cite This Article
APA
Avellar HK, Lutter JD, Ganta CK, Beard W, Smith JR, Jonnalagadda N, Peloquin S, Kang Q, Ayub K.
(2022).
In vitro antimicrobial activity of equine platelet lysate and mesenchymal stromal cells against common clinical pathogens.
Can J Vet Res, 86(1), 59-64.
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
Lutter, John D
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
Ganta, Charan K
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
Beard, Warren
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
Smith, Joseph R
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
Jonnalagadda, Naveen
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
Peloquin, Sarah
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
Kang, Qing
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
Ayub, Kanwal
Department of Clinical Sciences (Avellar, Lutter, Beard), Department of Diagnostic Medicine/Pathobiology (Ganta, Smith, Jonnalagadda, Peloquin), College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA; Department of Statistics, College of Arts and Sciences, Kansas State University, Manhattan, Kansas, USA (Kang, Ayub).
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