Sofie Van Meervenne

The influence of sex hormones on seizures in dogs and humans.

Epilepsy is the most common chronic neurological disorder in both humans and dogs. The effect of sex hormones on seizures is well documented in human medicine. Catamenial epilepsy is defined as an increase in frequency and severity of seizures during certain periods of the menstrual cycle. Oestradiol increases seizure activity and progesterone is believed to exhibit a protective effect. The role of androgens is controversial and there is a lack of research focusing on androgens and epilepsy. Indeed, little is known about the influence of sex hormones on epilepsy in dogs. Sterilisation is believed to improve seizure control, but no systematic research has been conducted in this field. This review provides an overview of the current literature on the influence of sex hormones on seizures in humans. The literature on idiopathic epilepsy in dogs was assessed to identify potential risk factors related to sex and sterilisation status. In general, there appears to be an over-representation of male dogs with idiopathic epilepsy but no explanation for this difference in prevalence between sexes has been reported. In addition, no reliable conclusions can be drawn on the effect of sterilisation due to the lack of focused research and robust scientific evidence.

Magnetic stimulation of the radial nerve in dogs and cats with brachial plexus trauma: A report of 53 cases

Brachial plexus trauma is a common clinical entity in small animal practice and prognostic indicators are essential early in the course of the disease. Magnetic stimulation of the radial nerve and consequent recording of the magnetic motor evoked potential (MMEP) was examined in 36 dogs and 17 cats with unilateral brachial plexus trauma. Absence of deep pain perception (DPP), ipsilateral loss of panniculus reflex, partial Horners syndrome and a poor response to MMEP were related to the clinical outcome in 29 of the dogs and 13 of the cats. For all animals, a significant difference was found in MMEP between the normal and the affected limb. Absence of DPP and unilateral loss of the panniculus reflex were indicative of an unsuccessful outcome in dogs. Additionally, the inability to evoke a MMEP was associated with an unsuccessful outcome in all animals. It was concluded that magnetic stimulation of the radial nerve in dogs and cats with brachial plexus trauma may provide an additional diagnostic and prognostic tool.

Short-and-long-term outcome in 63 dogs treated conservatively or surgically for disc associated wobbler syndrome

Adiponectin has been investigated widely due to its association with adiposity and the metabolic syndrome in human beings. Adiponectin circulates as low- (LMW) and high-molecular weight (HMW) multimers and the latter are the more bioactive forms. There are no reports of the relative proportion (distribution) of adiponectin multimers in feline plasma. The aim of this study was to assess the association of dietary nutrient composition, body weight gain, meal feeding, and insulin sensitivity with HMW adiponectin concentration and adiponectin multimer distribution in cats.1 EVALUATION OF FOUR DNA EXTRACTION METHODS FOR THE DETECTION OF TRITRICHOMONAS FOETUS IN FELINE STOOL SPECIMENS BY POLYMERASE CHAIN REACTION. SH Stauffer, AJ Birkenheuer, MG Levy, H Marr, JL Gookin. College of Veterinary Medicine, North Carolina State University, Raleigh, NC. Feces are increasingly recognized as practical samples for molecular diagnosis of infectious disease. Extraction of PCR-quality DNA from feces can be challenging due to co-extraction of PCR inhibitors. Accordingly, we examined the effect of four commercially-available DNA extraction methods on sensitivity of PCR for detection of Tritrichomonas foetus (TF) in naturally-infected and TF-spiked feline stool. Kits evaluated included ExtractMaster Fecal DNA Extraction Kit, Epicentre Biotechnologies (Kit A); QIAamp DNA Stool Mini Kit, Qiagen (Kit B); UltraClean Fecal DNA Kit, MoBio (Kit C); and ZR Fecal DNA Kit, Zymo Research (Kit D). In accordance with manufacturer instructions, DNA was extracted from 180mg (A,B), 50mg (C), 100 & 150mg (D) aliquots of feline feces to which was added 20ml volumes containing 0–10,000 cultured feline TF. Each kit was also used to extract DNA from the feces of each of 10 naturally infected and 10 uninfected cats. DNA was eluted in 300ml (A), 200ml (B), 50ml (C), or 100ml (D) of respective elution buffer. Endogenous PCR inhibitors in extracted DNA was examined by PCR amplification of an 876 bp gene fragment of bacterial 16S rRNA. DNA was then tested by single tube nested PCR for amplification of partial ITS1, 5.8S and ITS2 rRNA genes of TF. Kit D provided the most sensitive detection of TF DNA as expressed by both organisms per DNA extraction and organisms per PCR reaction. To account for differences in DNA concentrations between kits (i.e. fecal sample size and elution volumes), the limit of detection for each kit as expressed by the number of TF per PCR reaction was as follows: Kit B 5 250, Kit A 5 167, Kit C 5 100, Kit D (150mg fecal sample) 5 5, and Kit D (100mg fecal sample) 5 0.5. PCR performed on DNA extracted from cultured TF (no feces) or TF-spiked feces (100mg) using Kit D was positive with as few as 10 TF per extraction. Further, DNA extraction using Kit D could be completed in the shortest time of all kits tested. These studies identify the ZR Fecal DNA Kit as superior to the other kits tested for extraction of PCR-qualityDNA from feline feces. ABSTRACT #2 INVESTIGATION OF ENTEROBACTER CLOACAE INFECTIONS AT A SMALL ANIMAL VETERINARY TEACHING HOSPITAL. JS Weese. University of Guelph, Guelph, Ontario.2 INVESTIGATION OF ENTEROBACTER CLOACAE INFECTIONS AT A SMALL ANIMAL VETERINARY TEACHING HOSPITAL. JS Weese. University of Guelph, Guelph, Ontario. A wide range of pathogens can cause hospital-associated (HA) infections in small animal hospitals. Among these is Enterobacter cloacae, which is one of the most clinically relevant Enterobacter spp and a common cause of HA infection in humans. Recently, multidrug resistance has become a concern, particularly with emergence of extended-spectrum beta-lactamase and extended spectrum cephalosporinase producing strains. An infection control investigation was initiated at the Ontario Veterinary College Teaching Hospital (OVCTH) in the fall of 2007 in response to anecdotal concerns about Enterobacter cloacae infections in hospitalized animals. Enterobacter cloacae was isolated from 45/36719 animals from January 1, 2005 to October 31, 2007, for an overall incidence of 1.2/ 1000 admissions. The monthly incidence rate ranged from 0 to 4.3/ 1000 admissions. Twenty-one (47%) cases were classified as community-associated, while 17 (38%) were hospital associated. Seven (15%) were community-onset but hospital associated, with three of these associated with other veterinary hospitals. There was no increase in the incidence of overall or hospital-associated infections during the study period. The urinary tract was the most common site of infection (n511, 24%). Wound infections (excluding surgical site infections) accounted for 8 (18%) of infections, with superficial and deep surgical site infections accounting for 7 (16%) and organ/space surgical site infections accounting for another 2 cases. Urinary tract infections were most common among animals with CA infection, accounting for 8/21 (38%) cases with wound infections accounting for 4 (19%) cases. Of the 24 cases associated with the OVCTH, 17 (71%) had surgery, 15 (63%) were hospitalized in the intensive care unit, 10 (42%) had indwelling urinary catheters placed, and 20 (83%) had received antimicrobials prior to onset of infection. Risk factors for E. cloacae infection could not be determined because a noninfected control group was not evaluated. Surgical site infections accounted for 9 (38%) HA cases. Overall, only 2/11 (18%) urinary tract infections were associated with prior placement of a urinary catheter. Nine (20%) animals died or were euthanized and E. cloacae was implicated as a causative or contributing factor in 5 (56%) of those cases. Two main antimicrobial phenotype patterns were identified. One (n525) was characterized by susceptibility to fluoroquinolones, tetracycline, and trimethoprim with variable susceptibility to cefoxitin while the other (n514) was characterized by resistance to these antimicrobials. Prior administration of antimicrobials was associated with presence of the more resistant phenotype (P50.044) but there was no association between this phenotype and origin of infection (P50.74) and no increase in the prevalence of this phenotype from 2005 to 2007 (P50.97). Infections with this phenotype were not associated with nonsurvival (P50.74). There was no evidence of a, HA outbreak or increase in prevalence, yet identification of multidrug resistant E. cloacae in both CA and HA infections is concerning and requires ongoing surveillance. ABSTRACT #3 STAPHYLOCOCCUS PSEUDINTERMEDIUS: A NEWLY RECOGNIZED PATHOGEN IN DOGS AND CATS. MC Faires, D Slavic, JS Weese. Ontario Veterinary College, Animal Health Laboratory, University of Guelph, Guelph, Ontario.3 STAPHYLOCOCCUS PSEUDINTERMEDIUS: A NEWLY RECOGNIZED PATHOGEN IN DOGS AND CATS. MC Faires, D Slavic, JS Weese. Ontario Veterinary College, Animal Health Laboratory, University of Guelph, Guelph, Ontario. Staphylococcus intermedius has typically been regarded as the predominant pathogenic Staphylococcus spp in dogs and cats, and a leading cause of skin and soft tissue infections. In 2005, a novel Staphylococcus species, Staphylococcus pseudintermedius, was identified. This organism is closely related to, but distinct from, S. intermedius. Gene-sequence based methods are required to differentiate these two species; however, these techniques are rarely performed in clinical laboratories, and as a result the prevalence and characteristics of S. pseudintermedius are poorly understood. Recent evidence suggests that S. pseudintermedius may actually be the predominant Staphylococcus spp in dogs and cats but misidentified as S. intermedius by diagnostic laboratories. The objective of this study was to use sequence based methods to identify putative S. intermedius isolates from dogs and cats and to evaluate antimicrobial resistance and virulence factors among S. pseudintermedius isolates. Isolates from dogs and cats identified as S. intermedius by conventional laboratory methods were obtained from the University of Guelph Animal Health Laboratory. Isolates were collected in a serial manner without selection. DNA was extracted, sequencing of the sodA gene was performed, and isolates were identified via sequence alignment with reference staphylococcal strains through GenBank (www.ncbi.nlm.nih.gov/blast/BLAST.cgi). Antimicrobial susceptibility testing was performed and PCR was used to identify various virulence factors and antimicrobial genes. A total of 25 isolates were obtained from 21 dogs and 2 cats. Medical records were not available for 2 of the isolates. 25/25 (100%) were identified as S. pseudintermedius Severity of infection ranged from superficial dermatitis to rapidly fatal necrotizing fasciitis with the majority of isolates from otitis externa 9/23 (39.1%) and urinary tract infections 6/23 (26.1%). Antimicrobial susceptibility was as follows: amoxicillin/clavulanate 23/23 (100%), ampicillin 7/ 23 (30.4%), cephalothin 23/23 (100%), clindamycin 18/23 (78.3%), gentamicin 23/23 (100%), tetracycline 18/23 (78.3%), and trimethoprim/sulfa 19/23 (82.6%). Not all antimicrobials were tested for all isolates, based on laboratory protocols regarding antimicrobial panel and site of infection. Inducible resistance to clindamycin was detected by D-test in 1 isolate reported as clindamycin-susceptible (5.6%). Detection of virulence factors and antimicrobial resistance genes is ongoing. This study identified S. pseudintermedius as an important pathogen in dogs and cats, and suggests that S. intermedius may not be a major concern in these species. Further studies are required to evaluate clinically relevant virulence factors to assist in understanding the pathogenesis of disease caused by S. pseudintermedius. 70