Considerable research on ticks has been done since it was discovered that the Rocky Mountain wood tick, Dermacentor andersoni Stiles, was a principal vector of Rocky Mountain spotted fevero Additional disease agents of man are also transmitted by D. andersoni. This tick and a closely related species, Dermacentor parumapertus Neuman, occur commonly in Utah. The two species are often closely associated, although D. andersoni is believed to occur in the mountains, whereas D. parumapertus is in the desert valleys. Diseases affecting animals in nature are transmitted by ticks of both species. Consequently, any interaction between the two may be influential in the maintenance of diseases in nature communicable to man and his domestic animals.

Malignant catarrhal fever (MCF), a disease that is usually fatal in cattle, is caused by two distinct but related bovine herpesviruses which are members of the genus Macavirus. The wildebeest-associated alcelaphine herpesvirus-1 (AlHV-1) occurs mainly in East and southern Africa, whereas the sheep-associated ovine herpesvirus-1 (OvHV-2) has an almost worldwide distribution. The natural hosts or carriers of these two viruses are subclinically infected. The 130 kilobase pair (kbp) AlHV-1 double stranded DNA genome consists of 18 open reading frames (ORFs) coding for structural proteins and approximately 50 ORFs coding for non-structural proteins. The 18 structural ORFs encode for 4 capsid proteins, 5 tegument proteins, 8 glycoproteins and a minor capsid scaffold protein. ORF8 encoding for glycoprotein B, is the most conserved of the proteins amongst gammaherpesviruses, whereas the minor capsid protein encoded by ORF65, is amongst the most variable. Thus, the minor capsid protein is one of the antigens of choice for the development of an ELISA for detection of AlHV-1 reactive antibodies and glycoprotein B could be of importance in developing a cross-protective vaccine for gammaherpesviruses. The naming and annotation of most of the AlHV-1 ORFs is based on comparison with related gammaherpesviruses and bioinformatics. Most of these ORFs are putative as there is no direct experimental evidence confirming that they code for any particular protein. In order to investigate whether the ORFs code for any proteins, two ORFs were targeted for in vitro heterologous expression. AlHV-1, isolate C500, was grown in fetal bovine turbinate (BT) cell culture and viral genomic DNA extracted. ORF8, the putative glycoprotein B, was amplified with a PCR assay and inserted into a mammalian expression vector, pCI. VERO cells were transfected with the recombinant vector. Expression of ORF8 was confirmed by an indirect immunofluorescence assay (IFA) with AlHV-1 polyclonal sera and rabbit anti-bovine IgG (whole molecule) FITC conjugate. Truncated forms of ORF8 were further expressed as baculovirus recombinants using the Bac-to-Bac baculovirus expression system. Expression of the truncated ORF8 was confirmed by SDS-PAGE and Western blot. AlHV-1 ORF65, the minor capsid protein gene, was amplified with a PCR assay from the viral genomic DNA and cloned in frame with a histidine tag in a bacterial expression vector, pCOLD I. Expression of the minor capsid protein was confirmed by SDS-PAGE and Western blot with the histidine tag monoclonal as well as AlHV-1 polyclonal sera. Orf65 was expressed in large quantities and column purified using the histidine tag. Orf65 was also expressed as a baculovirus recombinant using the Bac-to-Bac baculovirus expression system. Expression of the protein was confirmed by SDS-PAGE and Western blot with the histidine tag and AlHV-1 polyclonal sera. ORF65 expression in the baculovirus Bac-to-Bac expression system was up-scaled and the expressed protein column purified. Antibodies raised in chicken against the purified antigen were used successfully in an indirect immunoassay to detect AlHV-1 infected cells. An indirect enzyme-linked immunosorbent assay (ELISA) to detect antibodies against AlHV-1 was developed. It is based on the use of the AlHV-1 minor capsid protein as the capture antigen for antibodies. The primary antibodies are detected by the addition of enzymelabelled (horseradish peroxidase) protein G which detects bovid, ovid and wildebeest antibodies. Addition of a substrate of the enzyme, in this case, 3,3’,5,5’- tetramethylbenzidine (TMB), results in a colour reaction which is measured using spectrophotometric procedures. At a selected cut-off point of 18, the ELISA test has a sensitivity of 100% and a specificity of 100% and has been shown to detect AlHV-1 antibodies in cattle and wildebeest. The ELISA showed no cross-reactivity with sera raised in cattle against related viruses such as ovine herpesvirus 2, bovine herpesvirus 1, 2 and 4. The two expressed proteins used in this study were found to be amongst the antigens expressed in cattle suffering from malignant catarrhal fever. The experimental AlHV-1 indirect ELISA needs further validation and this research may be extended to determine the performance of these antigens as candidate subunit vaccines. / Dissertation (MSc)--University of Pretoria, 2013. / gm2014 / Veterinary Tropical Diseases / unrestricted

During March 2008 a suspected outbreak of Rift Valley fever was reported on a farm in the Bela-Bela area, Limpopo Province of South Africa. The affected dairy farm, where no vaccination programme against RVF were practiced, applies an intensive farming system with 300 Holstein Friesland cattle (calves included) as well as 200 Pedi sheep on the farm. Seven calves died on this farm but no apparent clinical disease was reported in cattle as well as in sheep. During the outbreak blood samples from cattle and sheep were taken and the animals were re-sampled 8 weeks later. A set of sera was also collected from cattle on a neighbouring farm. The aim of the study was to determine the extent of the outbreak by evaluating if the virus had also infected other animals on the affected farm as well as on a neighbouring farm. During the first blood collection 233 samples were taken from cattle and 73 from sheep on the affected farm; 55 blood samples were taken from cattle on a neighbouring farm. A second blood collection was only done on the affected farm and 234 cattle and 85 sheep were bled. All the sera collected were tested by an IgM-capture ELISA and by an indirect IgG ELISA. Selected IgM positive (n=14), IgG positive (n=23) and samples negative for both IgM and IgG (n=19) were then tested by the serum neutralization test (SNT). Sera from IgM positive (14) and negative (20) animals were also tested by a TaqMan PCR. Results from the affected farm showed that 7% (16/233) of cattle samples were IgMpositive and 13.7% (32/233) IgG positive at the first collection of samples, and 2% were IgM-positive at the second sample collection. The number of cattle positive for RVF virus-specific IgG antibodies increased by 20.3% when compared to the first bled. Only 1.4% of sheep were both positive for anti-RVF virus IgM and IgG antibodies at the first collection; IgM-positive cases decreased to 1.2%, while IgG-positive cases increased to 2.4% at the second bled. Although no IgM-positive cattle could be found on the neighbouring farm, 5.5% of cattle were IgG-positive. The SNT confirmed most of the ELISA results. Three samples that tested positive for anti-RVF virus IgM and one anti-RVF virus IgG positive sample using ELISA tested negative using the SNT. Two samples that tested negative for both IgM and IgG antibodies using ELISA, tested low positive (1:10 and 1:20) using the SNT. All samples tested using a TaqMan PCR were negative. On the affected farm, apart from the seven calves that died, cattle were also infected. There was evidence of virus circulation on the neighbouring farm but the negative PCR results indicate that at the time the animals were sampled they were not viraemic. How the virus was introduced onto the farm is not clear. The possibility of low level virus circulation in animals and the reactivation of virus from endemic foci by the breeding of vector competent mosquitoes on the low-lying area on the farm in Bela-Bela may have led to ideal circumstances for an outbreak to occur. The fact that mostly cattle seroconverted suggests a higher host preference of the local population of mosquitoes for cattle rather than sheep. Copyright / Dissertation (MSc)--University of Pretoria, 2011. / Veterinary Tropical Diseases / unrestricted

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AN ABSTRACT OF THE THESIS OFZachary Alley, for the Master of Fine Arts degree in Technical Direction, presented on March 27, 2022, at Southern Illinois University Carbondale. TITLE: I HAVE A FEVER FOR MORE PEACOCKS: TECHNICAL DIRECTION FOR HAY FEVER MAJOR PROFESSOR: Thomas FagerholmThe Hay Fever production was produced on December 2, 2021 at Southern IllinoisUniversity Carbondale’s School of Theater and Dance. This thesis will pull the reader through the ideas, planning, and construction of the realized scenic design that composed the work of the technical director on this production. Focuses on how the technical director maintained open communication between the production team throughout the process. The technical director strived to bring clear interpretations of the scenic elements into their drafting to be used by the build crews to make the set a reality within the time and budget. Hopefully by presenting this thesis to the reader they can have a more extensive understanding that the work of technical direction is even more involved than just the material world of set construction.

Background: Infective endocarditis is a rare but severe condition associated with a high mortality rate in small animal patients. This condition is caused by a microbial (most often bacterial) infection of the valvular portion of the endocardium, from which proliferative and/or erosive lesions on the cardiac valves or immediately adjacent structures develop. The two most commonly affected cardiac valves are the aortic and mitral valves. Case presentation: We report the clinical case of a 4-year old male neutered Bull terrier, 27.6 kg, body condition score 4/9, that presented with a 3-months history of pyrexia and general weakness. The patient history also revealed a transient left hind limb lameness (grade 2/4), which coincided with the onset of clinical signs about 3 months before presentation. On physical examination, a left-sided systolic heart murmur (grade 3/6) with the same intensity at the left heart base and apex, and an irregularly irregular heart rhythm were noted. Electrocardiography showed ventricular premature complexes, and echocardiography revealed lesions consistent with endocarditis involving the aortic and mitral valve. Bacterial culture of blood yielded a positive result, and the organism isolated was identified as Erysipelothrix rhusiopathiae. The extended patient history revealed that the dog lived close to a farm housing pigs and other livestock. Conclusion: We report a rare case of the premortal diagnosis of infective bacterial endocarditis in a dog due to E. rhusiopathiae infection. Most reports about this condition are from necropsy series. This clinical case report emphasizes that E. rhusiopathiae infection and bacteremia should be considered as a differential diagnosis in dogs with suspected infective endocarditis, especially in dogs living in rural areas with access to livestock and particularly farm pigs. Also, particular emphasis should be placed on the zoonotic potential of this infectious disease.

The objectives of this study were to determine (1) the prevalence of adult ticks of Dermacentor andersoni in national forest recreational sites of Utah, and (2) the incidence of spotted fever rickettsia, Rickettsia rickettsii, in the ticks of these areas. With the use of a white flannel cloth, 358 adult D. andersoni (135 males and 223 females) were collected from 48 recreational sites during the spring and summer of 1964. Ticks from each collection were put in pools, preserved in non-fat skim milk at -30° C, and subsequently tested for the presence of spotted fever rickettsia by guinea pig inoculations. The average collection rate (population density) for all collections was 6.8 per hour, but populations varied between sites. Populations were greater in the middle and southern parts of the state than in the northern. The greatest populations were at elevations between 6,000 and 8,000 feet with the upper limit just under 9,000 feet. The elevational distribution varied with the latitude--greater populations were found at higher elevations in southern than in northern Utah. The season of peak abundance was between the last week of May and the last of June. Populations were greater at lower elevations early in the season and at higher elevations later. Male ticks were more abundant early in the spring whereas females predominated later. The preferred habitat was open, unshaded areas of short, scanty, young grass. Ticks were collected in greater numbers in the afternoon than in the morning. Temperatures between 12° and 38° C apparently had little effect on tick activity. Activity was slightly greater on partly cloudy and cloudy days than on clear days, and increased proportionately relative to an increase in wind velocity. Spotted fever rickettsia were found in 3.6% of the ticks collected. These were from 13 different recreational sites, over half of which are in the northern half of the state near human population centers. Ticks positive for spotted fever were probably infected with avirulent type U or type T strain of R. rickettsii.

Predictive models based in symptomatology of suspected dengue patients seeking medical care in Honduras. The models based on logistic regression models predicted the outcomes of dengue fever/ severe dengue. Sensitivity and specificity are discussed. It also describe the level of agreement between Honduran classification of severe dengue and the ones based on World Health Organization guidelines of 1997 and 2009. / Introduction: Dengue is a major public health problem in tropical and subtropical countries but its clinical presentation may be similar to many febrile illnesses. Since in endemic countries laboratory confirmation is frequently delayed, the majority of dengue cases are diagnosed based on patient’s symptomatology. This can often lead to misdiagnosis and potential serious health complications. The objective of this study was to identify clinical, hematological and demographical parameters that could be used as predictors of dengue fever among patients with febrile illness. Methods: We conducted a retrospective cohort study of 548 patients presenting with febrile syndrome to the largest public hospitals in Honduras. Patients’ clinical, laboratory, and demographical data as well as dengue laboratory confirmation by either serology or viral isolation were used to build a predictive statistical model to identify dengue cases. Results: Of 548 patients, 390 were confirmed with dengue infection while 158 had negative results. Univariable analysis revealed seven variables associated with dengue: male sex, petechiae, skin rash, myalgia, retro-ocular pain, positive tourniquet test, and bleeding gums. In multivariable logistic regression analysis, retro-ocular pain petechiae and bleeding gums were associated with increased risk, while epistaxis and paleness of skin were associated with reduced risk of dengue. Using a value of 0.6 (i.e., 60% probability for a case to be positive based on the equation values), our model had a sensitivity of 86.2%, a specificity of 27.2%, and an overall accuracy of 69.2%; allowing for the diagnosis of dengue to be ruled out and for other febrile conditions to be investigated. Conclusions: The application of predictive models can be valuable when laboratory confirmation is delayed. Among Honduran patients presenting with febrile illness, our data reveal key symptoms associated with dengue fever, however the overall accuracy of our model is still low and specificity remains a concern. Our model requires validation in other populations with similar pattern of dengue transmission. Key Words: Dengue, fever, Predictive model, symptoms, Honduras / Thesis / Doctor of Philosophy (PhD) / Predictive models based in symptomatology of suspected dengue patients seeking medical care in Honduras. The models based on logistic regression models predicted the outcomes of dengue fever/ severe dengue. Sensitivity and specificity are discussed. It also describe the level of agreement between Honduran classification of severe dengue and the ones based on World Health Organization guidelines of 1997 and 2009.