No abstract

Reliable diagnostic tests are essential for disease investigation and management. This is particularly true for diseases of free-ranging wildlife where sampling is logistically difficult precluding retesting. Clinical assays for wildlife diseases frequently vary among laboratories because of lack of appropriate standardized commercial kits. Results of diagnostic testing may also be called into question when investigators report different etiologies for disease outbreaks, despite similar clinical and pathologic findings. To evaluate reliability of diagnostic testing for respiratory pathogens of bighorn sheep (Ovis canadensis), we conducted a series of ring tests across 6 laboratories routinely involved in detection of Mycoplasma ovipneumoniae, Pasteurellaceae, lktA (the Pasteurellaceae gene encoding leukotoxin), and 3 reference laboratories. Consistency of results for replicate samples within laboratories was high (median agreement ¼ 1.0). Agreement between laboratories was high for polymerase chain reaction (PCR) detection of M. ovipneumoniae and culture isolation of Mannheimia spp. and Bibersteinia trehalosi (median agreement ¼ 0.89-0.95, Kappa ¼ 0.65-0.74), and lower for PCR detection of Mannheimia spp. lktA (median agreement ¼ 0.58, Kappa ¼ 0.12). Most errors on defined status samples were false negatives, suggesting test sensitivity was a greater problem than specificity. However, tests for M. haemolytica and lktA yielded some false positive results. Despite differences in testing protocols, median agreement among laboratories and correct classification of controls for most agents was !0.80, meeting or exceeding the standard required by federal proficiency testing programs. This information is valuable for interpreting test results, laboratory quality assessments, and advancing diagnosis of respiratory disease in wild sheep. Published 2016. This article is a U.S. Government work and is in the public domain in the USA.

The safety and marked in vitro antiviral activity against noncytopathic BVDV, cytopathic BVDV, and VSV suggest that interferons alfa-2a and alfa-B/D may be useful for treatment of natural disease after infection with these viruses.

The precision and accuracy of a prototype wearable liquid crystal monitor (LCM) for the measurement of airborne organophosphate pesticide concentrations was explored in a series of laboratory experiments. LCM response to vapor-phase and aerosol diazinon was compared to concentrations obtained using a standard reference method (NIOSH 5600) at concentrations ranging from approximately 8 to 108 ppb (parts per billion) over durations of 2 to 80 hours. Temperature ( approximately 25, 30, and 35 degrees C) and relative humidity (15, 50, and 85%) were varied to estimate the effect of these factors on LCM performance. The LCM response to vapor phase pesticide exposure was linear for concentrations in the range of 8-20 ppb. At exposure concentrations above approximately 20 ppb, however, there was a decline in monitor response and measurement precision. Elevated temperatures improved diazinon vapor-only measurement precision, while increased relative humidity reduced LCM response at the extremes of tested temperatures. Compared to vapor-only exposures, the LCM was less sensitive to diazinon aerosol concentrations, but displayed reasonable precision over a relatively large range of exposures (29 to 1190 ppb-hr). Further efforts to characterize temperature and humidity effects and improve low-end sensitivity would likely provide a portable personal exposure monitor or environmental sensor for this widely used class of pesticides.