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Biomedical subjects

R E Porter

Publications and source records attributed to R E Porter.

At least 19 recordsLinked to original sources

Validation of a modified PCR-based method for identifying mutant restricted ovulator chickens: substantiation of genotypic classification by phenotypic traits.

Upon photostimulation, restricted ovulator (RO) female chickens exhibit endogenous hyperlipidemia, develop atherosclerotic lesions, and generally fail to lay eggs. This phenotype results from a point mutation in the gene specifying the very low density lipoprotein receptor (VLDLR), whose protein product normally mediates the massive oocytic uptake of egg yolk precursors from the circulation. Taking advantage of the single base change in the mutant VLDLR allele, a PCR-based method for the rapid identification of RO chickens was developed at the Biocenter and University of Vienna, Austria. However, this procedure was incompletely validated because phenotypic data were not obtained and conventional progeny testing of sons and grandsons was not performed. Here, the assay validation was completed by providing plasma lipid concentrations, plasma very low density lipoprotein particle sizes, or egg production records of PCR-genotyped females and their brothers and sires to demonstrate that each bird's phenotypic traits substantiated their genotypic classification. Moreover, several methodological modifications resulted in improved chemical safety, speed, and cost of preparing and analyzing genomic DNA from chicken erythrocytes. Because the ovaries of mutant RO females generally contain numerous vitellogenic follicles in the absence of a functional oocyte plasma membrane VLDLR, the existence of an alternate system for the oocytic uptake of plasma very low density lipoprotein and vitellogenin is suggested, whereas a physiological explanation as to why some, but not all, mutant RO hens are able to ovulate and lay eggs is lacking.

Animals↗

Palatability of bird repellents to Rattus norvegicus.

The palatability to captive, mostly laboratory-bred, Norway rats (Rattus norvegicus) of cereal-based baits containing 0.02 g kg-1 brodifacoum, with and without bird-repellent additives, was compared in a no-choice experimental design. Methyl anthranilate (25 g kg-1), dimethyl anthranilate (25 g kg-1) and cinnamamide (2.5 g kg-1) reduced bait consumption by the rats, but all except one rat ate enough bait to receive a lethal dose. Cinnamamide (1 g kg-1), ortho-aminoacetophenone (0.1 g kg-1) and tannic acid (20 g kg-1) did not reduce bait consumption and all rats died after eating baits. The concentration of cinnamamide palatable to rats has only a low and short-lived repellency to birds, so it does not warrant further investigation. However, ortho-aminoacetophenone and tannic acid should now be field-tested for palatability to all three rat species in New Zealand and for repellency to native New Zealand birds.

4-Hydroxycoumarins↗

Select 3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors vary in their ability to reduce egg yolk cholesterol levels in laying hens through alteration of hepatic cholesterol biosynthesis and plasma VLDL composition.

The inability to markedly attenuate cholesterol levels in chicken eggs has led to speculation that cholesterol is essential for yolk formation and that egg production would cease when yolk cholesterol deposition was inadequate for embryonic survival. However, this critical level hypothesis remains unproven. Here, we determine the relative responsiveness of laying hens to three select inhibitors of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGR), the rate-limiting enzyme of cholesterol biosynthesis. A control diet, either alone or supplemented with one of two dietary levels (0.03 or 0.06%) of atorvastatin, lovastatin, or simvastatin, was fed to White Leghorn hens for 5 wk. Liver cholesterol concentrations (mg/g tissue) were decreased (P </= 0.05) by each HMGR inhibitor; however, total liver cholesterol (mg) did not differ among treatments. Microsomal hepatic HMGR activities were increased one- to twofold in all HMGR inhibitor-treated groups, while HMGR mRNA levels were unaffected. Diameters of plasma VLDL particles, the main cholesterol-carrying yolk precursor macromolecules, were reduced (P </= 0.05) only in hens fed 0.06% atorvastatin, and the particles contained 38% less total cholesterol (P </= 0.05) than controls. Plasma total cholesterol concentrations were lowered (P </= 0.05) by both doses of atorvastatin (-56, -63%) and simvastatin (-36,-45%). Egg cholesterol contents were maximally reduced by 46% (P </= 0.05), 7% (P > 0.05), and 22% (P </= 0.05) in hens fed the 0.06% level of atorvastatin, lovastatin, and simvastatin, respectively, while overall egg production [-19% (P </= 0.05), +4% (P > 0.05), and -3% (P > 0.05)], was much less affected. We concluded that cholesterol per se may not be an obligatory component for yolk formation in chickens and, as such, may be amenable to further pharmacological manipulation

Animals↗

Hyporesponsiveness of the systemic and mucosal humoral immune systems in chickens infected with Salmonella enterica serovar enteritidis at one day of age.

Newly hatched chicks lack immunological maturity, which could compromise their ability to respond to infection by pathogens such as Salmonella enterica serovar enteritidis (S. enteritidis; SE). A study was conducted in which chicks were infected with a sublethal dose of SE at 1 d posthatch, and the systemic and intestinal immune responses to the challenge were followed over time. Birds infected at this age experienced difficulty in clearing the infection, and 50% of the individual birds remained persistently infected until 23 wk of age. These birds exhibited only a marginal systemic and mucosal humoral immune response to the infection. No response or little response was observed 1 wk postchallenge; responses increased somewhat over time. On many of the sampling times, 50% or more of the culture-positive birds lacked a detectable plasma or intestinal response. Levels of 10(3) to 10(5) SE/g of feces could be found in the intestines of birds eliciting a good IgA response, indicating that, when these birds did respond mucosally, the IgA produced was incapable of clearing the organism once the infection was established. Birds infected during this time also experienced reduced ability to respond to vaccination. Compared with uninfected controls, depressed responsiveness to an S. enteritidis bacterin was observed in infected birds 1 and 2 wk after administration, whereas those individuals receiving an inactivated Newcastle disease vaccine (NDV) experienced a reduced response 4 and 6 wk postvaccination, indicating that the persistent infection affected the ability of the immune system to respond to homologous and heterologous antigens. These results demonstrate that exposure of chickens to SE early in life interferes with the ability of these individuals to respond humorally to the infection and to other antigenic stimuli; such effects can be observed for at least 23 wk.

Animals↗

Delayed-type hypersensitivity reaction induced in broilers by killed Staphylococcus aureus.

A trial was conducted to determine whether the delayed footpad reaction (DFR) induced by killed Staphylococcus aureus in chickens is a delayed-type hypersensitivity (DTH) reaction. Five criteria were used to assess DTH: 1) DFR with a peak response at 24 to 48 h postchallenge, 2) inhibition of monocyte/macrophage migration, 3) lymphocyte blastogenic response, 4) mononuclear cell infiltration at the challenge site, and 5) passive transfer of DFR by splenic lymphocytes. Broilers were sensitized twice with a s.c. injection in the neck of S. aureus antigen (150 microg/bird) diluted in polyethylene glycol at 3 and 4 wk of age. Controls were s.c. injected with polyethylene glycol. At 6 wk of age, a migration inhibition test was conducted before the birds were challenged intradermally with S. aureus antigen (75 microg/bird) in PBS in the right footpad. The left footpad was injected with PBS. The thickness of the footpad was measured at 0, 4, 24, and 48 h postchallenge to evaluate the DFR. After challenge, blood was collected for the lymphocyte blastogenesis assay. Birds were euthanatized, and both footpads were removed for histology. The spleens were collected aseptically; splenic lymphocytes were injected i.v. into recipient birds. Sensitized birds showed an increase in the DFR (P < 0.02) and blastogenic response (P < 0.01) compared with nonsensitized birds. Delayed footpad reaction reached a maximum response at 24 h postchallenge. The in vitro migration of monocytes/macrophages from sensitized birds was significantly inhibited (P < 0.01). The histological appearance of S. aureus-injected footpads was characterized by dermal edema and perivascular infiltrates of small lymphocytes and macrophages. Birds that received sensitized splenic lymphocytes had a significantly pronounced DFR following challenge with S. aureus when compared with birds that received nonsensitized lymphocytes (P < 0.0001). These results indicated that the DFR can be used as a standard in vivo test for cell-mediated DTH reaction induced by killed S. aureus antigen in chickens.

Animals↗

Delayed-type hypersensitivity reaction induced in broilers via trachea inoculation of killed Staphylococcus aureus.

A study was conducted to determine whether the delayed-type hypersensitivity (DTH) reaction to killed Staphylococcus aureus antigen in chickens could be induced through multiple intratracheal inoculations. Three criteria were used to assess DTH: 1) delayed footpad reaction (DFR) with a peak response at 24 to 48 h postchallenge, 2) inhibition of monocyte/macrophage migration, and 3) mononuclear cell infiltration at the challenge site. Broilers were sensitized three times with a s.c. injection in the neck or intratracheal inoculation of killed S. aureus in polyethylene glycol at 2, 3, and 4 wk of age. Controls were given polyethylene glycol with a s.c. injection in the neck or intratracheal inoculation. Migration inhibition tests were conducted at 6 wk of age. At 7 wk of age, all birds were challenged intradermally with S. aureus antigen in PBS in the right footpad. The left footpad was injected with PBS. The thickness of the footpad was measured at 0, 4, 24, and 48 h postchallenge to evaluate the DFR. Birds were euthanatized, and both footpads were removed for histopathological examination. Subcutaneously or intratracheally sensitized birds showed significant DFR compared with nonsensitized birds (P < 0.0001), which reached maximum response at 24 h postchallenge. The s.c. sensitization resulted in an inhibition of the in vitro migration of monocytes/macrophages (P < 0.0001), whereas intratracheally sensitized birds did not show migration inhibition of monocytes/macrophages. Histological examination showed typical perivascular infiltration of small lymphocytes in S. aureus-injected footpads from s.c. and intratracheally sensitized birds. These results indicate that multiple intratracheal inoculation, as well as s.c. injection of killed S. aureus antigen, can be used to induce a cell-mediated DTH reaction in chickens.

Animals↗

Bacterial enteritides of poultry.

Enteric bacterial infections in poultry pose a threat to intestinal health and can contribute to poor feed efficiency and livability of a flock. A variety of enteric bacterial diseases are recognized in poultry. Three of these bacterial diseases, necrotic enteritis, ulcerative enteritis, and spirochetosis, primarily infect the intestine, whereas other bacterial diseases, such as salmonellosis, colibacillosis, mycobacteriosis, erysipelas, and fowl cholera, affect a variety of organ systems in addition to the intestine. Diagnosis of bacterial enteritis requires monitoring of clinical signs in the flock and proper use of diagnostic methods such as necropsy, histopathology, bacteriology, and serology.

Animals↗

Assessing the sensitivity of egg yolk antibody testing for detecting Salmonella enteritidis infections in laying hens.

The identification of infected commercial poultry flocks has become a pivotal component of efforts to reduce the incidence of egg-associated transmission of Salmonella enteritidis to humans. To assess the sensitivity with which testing for specific antibodies in egg yolks can be applied to detect S. enteritidis infection in laying chickens, groups of hens were orally inoculated with either 10(3), 10(5), or 10(7) cfu of a phage type 13a strain of S. enteritidis. Eggs from these hens were collected for 4 wk after inoculation and yolk samples were tested for antibodies to S. enteritidis flagella by ELISA. All hens that were inoculated with 10(7) cfu of S. enteritidis were detected as infected by the egg yolk ELISA when eggs were tested individually, as were up to 66 and 35% of hens inoculated with 10(5) or 10(3) cfu, respectively. Even when yolks from infected hens were diluted 1:10 in yolk from uninfected hens, specific antibodies could still be found in eggs from 31% of hens given 10(7) cfu of S. enteritidis and 13% of hens given 10(3) cfu. These results demonstrate that egg yolk antibody testing can provide a highly sensitive indication of prior exposure to S. enteritidis, and should accordingly be useful for verifying the effectiveness of programs designed to reduce the incidence of S. enteritidis infection in poultry.

Animals↗

World Health Organisation--supervised interlaboratory comparison of ELISAs for the serological detection of Salmonella enterica serotype Enteritidis in chickens.

A collaborative exercise, supervised by the World Health Organisation, was set up to compare ELISAs used for the serological detection of Salmonella enteritica serotype Enteritidis in chickens. The aim was to ascertain how far agreement could be reached on the interpretation of optical density readings for high titre, intermediate titre and low titre sera. Two sets of sera were sent to 14 participants. The first set compared high, medium and low titre sera raised in specified-pathogen-free and commercial broiler breeder chickens. The second set comprised 20 sera of different antibody titres raised in commercial birds reared under laboratory conditions and sent blind. Both indirect and double-antibody sandwich blocking ELISAs were used with a number of different detecting antigens. With a few exceptions good agreement was reached on the interpretation of results obtained from high and low titre sera from the optical density obtained with a single serum dilution. Differences were observed in the interpretation of medium titre sera. The results suggested that most ELISAs produce reasonably comparable results and that practical problems may arise from interpretation of the results mainly as a result of the choice of the criteria used for differentiating sera obtained from infected and uninfected chickens. These problems are discussed.

Animals↗

Differential diagnosis of infectious laryngotracheitis from other avian respiratory diseases by a simplified PCR procedure.

A simple polymerase chain reaction (PCR)-based procedure was developed for the detection of avian infectious laryngotracheitis virus (ILTV) in chicken trachea, chorio-allantoic membrane (CAM), infected hepatoma cells and infectious cell culture supernatant. Samples were prepared by dilution in distilled water. After boiling and low speed centrifugation, samples were used for PCR analysis with two primers without special labeling. The PCR analysis for ILT virus could be completed in less than 8 h. Standard agarose gel electrophoretic analysis of the PCR products revealed a prominent band of 300 base-pairs in samples from ILTV-infected specimens, but not from specimens containing Newcastle disease virus, infectious bronchitis virus, avian adenovirus, fowlpox virus, Pachecoz or Marek's disease virus. One single ILTV infected cell or 10 plaque forming units of ILTV could be detected with this procedure. The procedure can be used for the identification of ILTV and the differentiation of ILTV from other avian respiratory tract infectants.

Animals↗

Effect of two different molting procedures on a Salmonella enteritidis infection.

Previous studies have shown that inducing a molt using feed removal exacerbated an intestinal infection by Salmonella enteritidis (SE). The current study was conducted to determine whether inducing a molt using a molt diet would still cause a pause in egg laying but not exacerbate an intestinal SE infection. In Experiments 1 and 2, hens were either provided ad libitum access to layer feed (control), fed 45 g molt diet (molt-feed) daily, or deprived of feed for 14 d (molted), and were orally infected with 1 x 10(7) SE on Day 4 of molt. Egg lay ceased in hens subjected to both molt treatments. The percentage of hens shedding SE did not differ among treatment groups in Experiment 1, whereas in Experiment 2 the molted hens had significantly higher shed rates than the controls on Days 10, 17, and 24 postinfection and the molt-feed hens on Days 17 and 24 postinfection. Compared with both fed groups of hens, the molted hens shed significantly more SE in Experiment 1 on Day 10 postinfection, and in Experiment 2 the molted hens shed significantly more SE on all 4 sampling days. In Experiment 3, subgroups of hens within each treatment group received serial 10-fold dilutions of SE and intestinal shedding of the organism in each subgroup was determined 7 d later. The 50% infectious dose (ID50) was calculated for each treatment group from these shedding results.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Effect of induced molting on the recurrence of a previous Salmonella enteritidis infection.

Previous work in the authors' laboratory had shown that hens infected with Salmonella enteritidis (SE) during the feed removal phase of an induced molt shed significantly more SE and more readily transmitted SE to uninfected hens in adjacent cages when compared with unmolted hens. A study was conducted to examine the effect of induced molting on the recurrence and horizontal transmission of a previous SE infection. Hens aged 59 and 69 wk in Trials 1 and 2, respectively, were infected with SE and then molted 21 days later. In Trial 1, more molted hens were SE-culture-positive on Days 38 (P < or = .005) and 45 (P < or = .005) postinfection, and these hens shed more SE on these days (P < or = .05 and P < or = .005, respectively) than unmolted hens. Horizontal transmission of SE to previously uninfected but contact-exposed hens in adjacent cages was also higher in the molted group than the unmolted group on Days 38 (P < or = .05) and 45 (P < or = .001). Molted, contact-exposed hens also shed significantly more SE than unmolted hens. In Trial 2, the molted infected hens shed progressively more SE than the unmolted hens but the differences were not significant. However, more molted contact-exposed hens became SE-positive at Day 31 (P < or = .05) and 38 (P < or = .005) and also shed more SE on these days (P < or = .05 and P < or = .01), respectively) than the unmolted hens. Serum and intestinal antibody titers to SE were also examined in Trial 2. Molting appeared to exert no effect on the serum SE titers, but antibody titers in the alimentary tract were lower in the molted hens than the unmolted hens on Days 45 (P < or = .005) and 52 (P < or = .05). In Trial 1, three of eight molted directly infected hens and two of eight molted contact-exposed hens produced any SE-contaminated eggs. In Trial 2, no SE-contaminated eggs were produced.

Animals↗

Effect of induced molting on the course of infection and transmission of Salmonella enteritidis in white Leghorn hens of different ages.

Previous work in the authors' laboratory had shown that inducing molt using a 2-wk feed removal protocol in 58- to 84-wk-old White Leghorn hens increased the severity of intestinal infection by Salmonella enteritidis (SE). As susceptibility to infection can be influenced by age, a study was conducted to compare the effect of the feed removal on infection by SE in 20-, 40-, and 74-wk-old hens. Birds were orally infected with 5 to 10 x 10(6) SE on Day 4 of fast and were sampled for SE shedding 3, 10, 17, and 24 days later. Significantly higher numbers of SE were shed in fasted birds on Day 3 (20 and 40 wk of age), Day 10 (40 and 74 wk of age), and Day 17 (74 wk of age). Transmission of SE to uninfected, contact-exposed birds was observed in all three trials for both the fed and fasted groups. However, significantly more fasted contact-exposed birds became positive for SE on Day 3 (20-wk-old), Day 10 (74-wk-old), and Day 17 (74-wk-old). Significantly more SE was also shed in these fasted contact-exposed birds on Day 3 (20-wk-old), Day 10 (all age groups), and Day 17 (74-wk-old). The current results indicate that the fasting conditions used to induce a molt in hens increase the shedding of SE in direct-infected and contact-exposed hens and this effect does not appear to be affected by age.

Aging↗

Development of an enzyme-linked immunosorbent assay to detect IgG, IgM, and complement (C3) on canine erythrocytes.

An ELISA was used to detect IgG, IgM, and complement (C3) on the surface of canine erythrocytes. Erythrocytes were placed in wells of a microtitration plate and incubated with affinity purified, alkaline phosphatase-conjugated anti-canine IgG, IgM, or C3. Results of the ELISA were compared with the direct antiglobulin test (DAT) by preparing standard reference curves from canine blood type A erythrocytes that had been incubated with serial dilutions (1:2 to 1:8, 192) of canine anti-A serum. The ELISA detected increased erythrocyte-bound immunoglobulin and complement at two- to fourfold dilutions greater than those required for positive results with the DAT. The ELISA required small sample and reagent volumes and detected lower concentrations of immune components than did the DAT.

Animals↗

Effects of body position and ventilation/compression ratios during cardiopulmonary resuscitation in cats.

Eighteen cats were anesthetized and were randomly assigned to 2 groups (9 cats/group). Cardiopulmonary resuscitation (CPR) was performed on each cat, with the cat in dorsal (group 1) or lateral (group 2) recumbency, by administering 5 external cardiac compressions/1 interposed (diastolic) ventilation (American Heart Association [AHA] technique; n = 3 cats/technique), simultaneous compression and ventilation (SCV; n = 3 cats/technique), or SCV with 1 interposed (diastolic) ventilation every tenth compression (SCV/DV; n = 3 cats/technique). Fourteen of the 18 cats were resuscitated. Central aortic and venous pressures were determined concurrently with lead II electrocardiography. Arterial blood samples were collected during the base-line period (after pressure fluctuations had stabilized, with the cats spontaneously breathing room air), 2.5 minutes after the onset of arrest (defined as the cessation of aortic pressure fluctuations), and after 10 minutes of CPR. Arterial blood gas values during the base-line period or during the period of arrest were not significantly different between group-1 and group-2 cats. After CPR, arterial pH and bicarbonate values were not significantly different between groups or between technique categories. The PaCO2 values were significantly lower in cats resuscitated by SCV or by SCV/DV than in cats resuscitated by AHA (P less than 0.05). The PaO2 values were significantly (P less than 0.001) higher in group-2 cats than in group-1 cats and were significantly (P less than 0.001) different between each technique category, with cats resuscitated by AHA having the lowest PaO2 and cats resuscitated by SCV/DV having the highest PaO2. Body position, CPR technique, sex, weight, or arterial blood gas values after CPR were not predictors of successful resuscitation.

Animals↗

Cross-country skiing. A benign sport?

Cross-country skiing has been thought to be a safe sport, with few serious injuries and a preponderance of upper extremity injuries. Eleven cases of relatively severe injuries illustrate that this is not necessarily true.

Adolescent↗

Financial aspects of clinical education to facilities.

The financial aspects of clinical education for full-time junior and senior physical therapy students as related to facilities offering clinical affiliatins were determined. A questionnaire concerning supervisory expenses, student support, direct and indirect costs returned by 35 facilities of all types provided the basic information. Comparisons of costs and revenues were made for junior and senior students separately and for facilities according to type, size,and personnel involved in student supervision.

Costs and Cost Analysis↗