These grants will be awarded by the ESVD for basic or clinical research in veterinary dermatology. Applicants will be expected to propose a project of scientific merit that is applicable to veterinary dermatology. The projects are expected to be of one to two year’s duration. Preference will be given to novel proposals including the development of pilot studies, but applications of ongoing research work will be also considered.
Types of research grants:
Information about grants awarded
Practitioner grant 2016
"Role of elastography in the evaluation of canine skin: principles and clinical considerations”
Eric Zini, Giordana Zanna, Giulia Brizzi , Edoardo Auriemma and Simona Morabito
Presentation of the study
Elastosonography is a painless, invasiveness and promising imaging method that allows the assessment of tissue elasticity. It is based on the principle that softer, normal tissue displaces more easily than harder, malignant tissue when an oscillatory pressure is manually applied by an ultrasound transducer. The variation in deformity is seen as changes in ultrasound signals which are represented on the video screen by a color map called elastogram. The increased tissue hardness appears in ascending order as red, yellow, green and blue.
In human medicine, elastosonography is currently used in several cutaneous and internal organ disorders as an intriguing alternative to the traditional diagnostic tools because it provides useful information about the stiffness and the anatomic features of a lesion. In dermatology, it has been used to evaluate cutaneous neoplasms as melanoma and carcinoma or diffuse cutaneous systemic sclerosis and lymphedema.
In veterinary, few reports are reported on the application of elastosonography on several tissues as liver, splenic and renal parenchyma or in mammary tumors. However, no studies have been performed about the use of elastosonography in veterinary dermatology.
The aim of this project is to correlate elastosonographic with histopathological findings of nodular lesions in dogs, in order to identify elastosonographic criteria that may provide further information to the clinician in the morphological screening of these lesions.
Major grant 2015
"Evaluation of the cutaneous immunological milieu and leptin expression in dogs naturally affected by Leishmania infantum/chagasi before and after meglumine antimoniate treatment"
Dr Antonio Di Loria and Dr Domenico Santoro
Presentation of the study:
Leishmaniasis is a wide spread infectious disease endemic in the Mediterranean area for both dogs and people. Although not completely elucidated, an alteration of the cutaneous immune response has been demonstrated in affected dogs. Multiple immunological cell types have been involved in the immunological response in affected animals. It is well known that a cell-mediated response (T helper [Th] 1 type) is the cornerstone of dogs’ resistance against the parasite; however no studies have been reported on the immunological status (innate and adaptive immunity) of naturally affected dogs before and after treatment with meglumine antimoniate. In people with cutaneous leishmaniasis treated with meglumine antimoniate, it has been shown that an enhancement of the phagocytosis and TNF-α production by peripheral monocytes is present compared with monocytes not exposed to antimoniate. No information is currently available on the involvement of innate immunity in canine leishmaniasis; the only exception is the proven in vitro efficacy of antimicrobial peptides (AMPs) against Leishmania parasite. In addition, very few biological markers, to rapidly identify the immunological response, are available in veterinary medicine. In people, biological molecules able to orchestrate the Th1 and Th2 immune response and their potentials for therapies against infectious agents have been investigated in the past few years. One of such markers is leptin, a hormone secreted primarily by adipocytes and immune cells. Very recently it has been shown that an increase in leptin mRNA expression is present in peripheral blood mononuclear cells in canine leishmaniasis compared with healthy dogs. This study supported the idea of leptin as possible marker of severity and prognosis in affected dogs. However, no studies have been published on the cutaneous expression of this marker in affected dogs and how leptin may orchestrate the local and systemic immune response. Thus, the specific aims of this study are: 1) to evaluate the cutaneous and circulating expression of leptin in affected dogs before and after antimoniate administration; 2) to investigate the cutaneous presence of lymphocyte cell types (Th1, Th2, T regolatory [Treg], and Th17), dendritic cells and AMPs in affected dogs before and after treatment; 3) to evaluate the cutaneous cytokine pattern in affected dogs before and after treatment. This study will elucidate the cutaneous immune response (innate and adaptive) in canine leishmaniasis before and after antimoniate therapy and how these changes relate to the clinical response. Also it will clarify the role of leptin as suitable biomarker for severity and prognosis of canine leishmaniasis. For this purpose ten healthy control dogs and fourteen dogs naturally infected by L. infantum will be used. Skin biopsies will be taken before (in all dogs) and after 30 days of standard therapy with meglumine antimoniate (in Leishmania affected dogs). Indirect immunofluorescence will be used to evaluate the number of cutaneous dendritic cells, Th1, Th2, Treg, and Th17. ELISA will be used to determine the amount of cutaneous cytokines (INF-γ, IL-4, IL-10, TGF-β, and IL-17), AMPs (β defensin [cBD]3 like, cBD103, and cathelicidin), and leptin.
Practitioner grant 2015
"To evaluate the response to oclacitinib administered at 1 mg/kg twice daily in allergic cats and compare it to methylprednisolone given at 1 mg/kg/day. "
Drs Borio, Noli, Colombo, Ortalda, Maina
Feline allergic dermatitis is a common disease in veterinary dermatology. Cases of allergic dermatitis not caused by food or flea allergens have been called “feline atopic-like disease” (ALD) or “non-flea, non-food induced hypersensitivity dermatitis” (NFNFIHD). Oclacitinib (Apoquel, Zoetis, Rome, Italy) has recently been registered for the treatment of allergic pruritus and atopic dermatitis in the dog and is able to quickly, safely and effectively inhibit pruritus and clinical signs of canine allergic dermatitis. Oclacitinib can be a very attractive option for the treatment of feline allergic diseases. There is scant information about the use of oclacitinib in allergic cats and a previous pilot study conducted by our group suggests that oclacitinib at a dosage of 0.4-0.6 mg/kg is able to suppress pruritus and clinical signs associated with skin allergy in cats, albeit only in less than 50% of the animals treated at the dosage used in the study. The aim of this double blinded randomized controlled study is to evaluate the response to oclacitinib administered at 1 mg/kg twice daily in allergic cats and compare it to methylprednisolone given at 1 mg/kg/day. This study will evaluate decrease of pruritus and lesional scores, as much as ease of administration, tolerability, development of adverse effects, and improvement of quality of life of cats and owners.
Training grant 2015
For "Ig based selection of elimination diets in dogs with food-induced dermatitis atopic"
Dr Ramón M. Almela and Dr Ursula Mayer
Presentation of the study
Adverse Food reaction is a common skin condition that can manifest clinically as canine atopic dermatitis. Currently, the gold standard diagnosis is based on elimination - rechallenge diet trials. To date, there is a consensus between veterinary dermatologists that the best way to select the best suitable diet is to collect a detailed dietary history, as far as possible. Hence, this method is very time consuming for both the vet and the owner and in addition favours pitfalls. Therefore, it seems that alternative tests in the diagnostic workup would be of benefit. Recent evidence suggest that in vitro testing for food allergens by IgE and/or IgG reflects previous exposure to selected food ingredients, thus, indicating that IgE and/or IgG negative results may be used effectively to select the ingredients for an elimination diet. In this study we aim to verify this hypothesis by means of a prospective controlled study to compare the gold standard selection of elimination diet ingredients by food history to the results of in vitro serum IgE/IgG for food allergens. The strengths of the study are i) non-invasive method, ii) would explore the effectiveness of an alternative test of ingredient selection in elimination diets which cloud be much easier and faster to perform and less proan to errors.
Practitioner grant 2014
"For evaluation of skin diseases in bats"
Anette Loeffler David Lloyd Kay Fountain
Presentation of the study
Many species of wild bat are declining in numbers or are endangered and may be taken into captivity as part of a conservation plan, when sick or injured, or as zoo exhibits. Although they vary in size from fruit bats with a five foot wing span down to the size of a bumble bee, they share a tendency to develop skin diseases which are often associated with bacteria. An unexplained outbreak of ear pinna disease caused the failure of a reintroduction project in New Zealand because loss of the ear pinna due to necrosis left the bats unable to echolocate. Skin disease affecting the delicate wing membranes in bats can be similarly debilitating, and spread of bacterial infection from the skin has led to deaths due to septicaemia, osteomyelitis and endocarditis.
In this study we will gather information from bat keepers to better understand the type and distribution of skin disease by questionnaire. We will also obtain cytology, histopathology and bacterial samples from skin lesions of affected bats in order to study the aetiology and progression of skin disease and ear pinna necrosis. Longer-term objectives include the epidemiological study of strains of S. aureus carried by bats, and their antimicrobial resistance profiles and toxin-production, in order to establish how these relate to strains associated with humans, livestock and domestic animals. The results from this project will be of interest to veterinary dermatology, to microbial evolution studies and to wildlife conservation.
Training grant 2013
For "Stem cell markers in the canine hair follicle: an approach to elucidate the location, quantity and marker expression in different hair cycle stages"
Dr Wiener Dr Welle
Dominique Wiener, Dr.med.vet., PhD, Dipl. ECVP, Vetsuisse-Faculty, University of Bern, Länggassstrasse 122, 3012 Bern, Switzerland, E-mail: firstname.lastname@example.org
Monika Welle, Prof. Dr.med.vet, Dipl. ECVP, Vetsuisse-Faculty, University of Bern, Länggassstrasse 122, 3012 Bern, Switzerland, E-mail: email@example.com
Presentation of the study
Non-inflammatory alopecia is a frequent problem in dogs; however, the pathogenesis is poorly understood. A hair cycle arrest, related to an impaired function of the stem cell compartment of the hair follicle is a likely cause. Therefore we examined the expression profile of follicular stem cell markers (Lgr5, Lgr6, Nestin, CD200, Keratin 15, CD34 and Sox9) in biopsies from healthy beagle dogs by qPCR, western blot analysis and immunohistochemistry. qPCR, cloning and sequencing confirmed expression of all markers in canine skin. Immunohistochemistry showed labeling of cells with Lgr5 only in the secondary germ of telogen hair follicles. CD34 stained the outer root sheath (ORS) cells of the isthmus in anagen and, to a lesser degree, in telogen hair follicles. Sox9 labeled cells in the innermost layer of the anagen ORS. K15 stained the basal cell layer of the ORS in anagen and the entire ORS in telogen, respectively. Nestin stained the dermal papilla and the lower end of the fibrous connective sheath (associated with the inferior portion) in the anagen hair follicle. Lgr6 and CD200 antibodies we tested, no specific immunostainings could be achieved. Our results provide the basis to gain new insights into the pathogenesis of alopecia in dogs. Furthermore, our results will aid to investigate the role of stem cells in the development of skin tumors.
This award resulted in an article in Journal of Histochemistry & Cytochemistry 64 (2016) 190-204: “Stem Cell-Associated Marker
Expression in Canine Hair Follicles.”
Practitioner grant 2013
For “Dermoscopy in dogs: an absorbing perspective in evaluation of pattern alopecia”
Giordana Zanna DVM, PhD, DipECVD: Studio Dermatologico Veterinario, Via Sismondi 62, 20133 Milan, Italy
Fabia Scarampella, DVM, MSc, DipECVD: Studio Dermatologico Veterinario, Via Sismondi 62, 20133 Milan, Italy
Sara Legnani, DVM: Studio Dermatologico Veterinario, Via Sismondi 62, 20133 Milan, Italy
Paola Roccabianca, DVM, PhD, DipECVP: Department of Pathology, Hygiene and Veterinary Public Health, University of Milan, Italy
Antonella Tosti MD Department of Dermatology & Cutaneous Surgery, Miller School of Medicine, University of Miami, FL, USA
The research will be performed at Studio Dermatologico Veterinario, Via Sismondi 62, 20133 Milan, Italy
Presentation of the study
Dermoscopy is a noninvasive, in vivo technique that aids in the visualization of cutaneous morphologic features that are not visible to the naked eye. In humans, trichoscopy (hair and scalp dermoscopy) is currently widely used in the evaluation of patients with hair loss disorders such as androgenic alopecia. The perspective of this research is to generate dermoscopic criteria useful for the diagnosis of pattern alopecia in dogs comparing dermoscopic and histopathological findings. A total of 30 young-adult short-coated healthy dogs will be included in the study and matched with 30 young short-coated dogs affected by noninflammatory, nonpruritic progressive alopecia attributable to pattern alopecia.
Major Grant 2013
Dr. Jon Golding and Dr. Jane Dobson.
Clinical trial of photodynamic therapy with glycolysis inhibition for equine sarcoids.
The award resulted in an article published in Veterinary and Comparative Oncology DOI 10.1111/vco.12299: “Glycolysis inhibition improves photodynamic therapy response rates for equine sarcoids.”
Practitioner grant 2012
"For examination of the role of antimicrobial peptides in skin defense in healthy and atopic canines"
Dr Chrisi Simou Dr Eleni Dotsika Dr Elpida Vingopoulou Dr MN Saridomichelakis
DVM, MSc, PhD, private practitioner, 12 M. Mousourou str, 11636, Athens, Greece,
DVM, PhD, Laboratory of Cellular Immunology, Dept. of Microbiology, Hellenic Pasteur Institute,Vas.Sofias 127 Av., Athens 115 21 Greece,
Victoria I Siarkou
PhD, DVM, MD, Assist. Professor, Lab. of Microbiology and Infectious Diseases, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, University Campus 54124, Greece,
Elpida Vingopoulou PhD candidate, Lab. of Microbiology and Infectious Diseases, Faculty of Veterinary Medicine, Aristotle University of Thessaloniki, University Campus 54124, Greece,
Manolis N. Saridomichelakis DVM, PhD, Dipl. E.C.V.D Accosiate Professor Clinic of Medicine, Faculty of Veterinary Medicine, University of Thessaly, Trikalon 224, GR-43100, Karditsa, Greece.
E- mail: firstname.lastname@example.org
Presentation of the study
The aim of this study is to clarify the role of antimicrobial peptides in the skin defense in healthy and atopic canine skin and to examine whether there is an interaction among antimicrobial peptide production from keratinocytes and skin microbial flora. The importance of the research is highlighted by the rise of resistant bacteria in canine pyoderma. We believe that we need to examine the intrinsic defense mechanisms of the skin and learn how to modify them in order to fight infections. In the long term we could clarify the reason for the susceptibility of the atopic canine skin to infections and whether a manipulation of the normal flora could act as a therapy for them.
Major grant 2012
"To determine the role of TLRs in the clinical outcome of L. infantum infection in dogs, characterizing TLRs and immune cytokines expression in skin from dogs with different stages of disease and immune responses."
The award resulted in an article published in Veterinary Parasitology 209 (2015) 157-163: “Histopathological findings and detection of Toll-like receptor 2 in cutaneous lesions of canine leishmaniosis"
Laura Ordeix i Esteve Laia Solano-Gallego Sergio Villanueva Saz Dolors Fondevila
Dolors Fondevila, DVM, PhD, Dipl. ECVP, Department de Medicina i Cirugia Animal, Facultat de Veterinaria, Universitat Autònoma de Barcelona, email@example.com
Sergio Villanueva Saz, DVM, Department de Medicina i Cirugia Animal, Facultat de Veterinaria, Universitat Autònoma de Barcelona, firstname.lastname@example.org
Laia Solano-Gallego, DVM, PhD, Dipl. ECVCP, Department de Medicina i Cirugia Animal, Facultat de Veterinaria, Universitat Autònoma de Barcelona, email@example.com
Project title: Characterization of Toll-like receptors and immune cytokines in cutaneous lesions from dogs with different stages of leishmaniosis and immune responses.
Presentation of the study
A broad range of immune responses and clinical manifestations have been described in canine Leishmania infantum infection. This variability ranges from "resistant" dogs displaying a protective Th1- cell- mediated immune response which induces anti- Leishmania activity in macrophages to severely sick dogs displaying a marked humoral immune response accompanied by reduced cell mediated immunity and a high parasite burden that is detrimental to the animal. Recent studies have shown that specific mediators of the innate immune system, such as toll-like receptors (TLRs), activate pro-inflammatory responses in Leishmania- infected macrophages resulting in elimination of the parasite in mouse models and in human beings. However, there is limited data available concerning the role that TLRs play in canine L. infantum infection.
The general aim of this study is to determine the role of TLRs in the clinical outcome of L. infantum infection in dogs, characterizing TLRs and immune cytokines expression in skin from dogs with different stages of disease and immune responses.
ESVD grant 2011
For "Risk factors for meticillin-resistant Staphylococcus pseudintermedius infection in dogs and cats"
Georg Lehner Tieraerztliche Spezialisten, Hamburg, Germany
Anette Loeffler The Royal Veterinary College, Hatfield, UK
Ross Bond The Royal Veterinary College, Hatfield, UK
David Lloyd The Royal Veterinary College, Hatfield, UK
Monika Linek Tieraerztliche Spezialisten, Hamburg, Germany
Collaborators: Nina Thom, Ellen Prenger-Berninghoff, Iris Straube