Detection of a genetic mutation for myotonia congenita among Miniature Schnauzers and identification of a common carrier ancestor

OBJECTIVE: To develop a molecular genetic test to detect the mutant skeletal muscle chloride channel (CIC-1) allele that causes myotonia congenita in Miniature Schnauzers and to analyze the relationship of affected and carrier dogs. ANIMALS: 372 Miniature Schnauzers from the United States, Canada, Australia, and Europe that were tested between March 2000 and October 2001. PROCEDURE: The sequence surrounding the mutation in the CIC-1 allele was amplified by use of a unique pair of primers. Polymerase chain reaction (PCR) products were digested with the restriction enzyme Hpy CH4 III and separated on a 6% polyacrylamide gel. Pedigrees from all available carrier and affected dogs were analyzed, and a composite pedigree was established. RESULTS: Enzyme digestion of PCR products of the normal CIC-1 allele resulted in 3 fragments of 175, 135, and 30 bp, whereas PCR products of the mutant allele resulted in fragments of only 175 and 165 bp. Of the 372 Miniature Schnauzers, 292 (78.5%) were normal, 76 (20.4%) were carriers, and 4 (1.1%) were affected (myotonic) dogs. Frequency of the mutant allele was 0.113. Pedigree analysis revealed that a popular sire, documented to be a carrier, was a common ancestor of all carriers and affected dogs. CONCLUSIONS AND CLINICAL RELEVANCE: A PCR-based enzyme digestion DNA test was developed. The mutant allele for this disease is frequent in Miniature Schnauzers that are related to a common carrier ancestor. Breeding dogs should be tested by this specific DNA test to help limit the spread of this deleterious mutation.     

A newly recognized blood group in domestic shorthair cats: the Mik red cell antigen

BACKGROUND: Naturally occurring alloantibodies produced against A and B red cell antigens in cats can cause acute hemolytic transfusion reactions. Blood incompatibilities, unrelated to the AB blood group system, have also been suspected after blood transfusions through routine crossmatch testing or as a result of hemolytic transfusion reactions. HYPOTHESIS: Incompatible crossmatch results among AB compatible cats signify the presence of a naturally occurring alloantibody against a newly identified blood antigen in a group of previously never transfused blood donor cats. The associated alloantibody is clinically important based upon a hemolytic transfusion reaction after inadvertent transfusion of red cells expressing this red cell antigen in a feline renal transplant recipient that lacks this red cell antigen. METHODS: Blood donor and nonblood donor cats were evaluated for the presence of auto- and alloantibodies using direct antiglobulin and crossmatch tests, respectively, and were blood typed for AB blood group status. Both standard tube and novel gel column techniques were used. RESULTS: Plasma from 3 of 65 cats and 1 feline renal transplant recipient caused incompatible crossmatch test results with AB compatible erythrocytes indicating these cats formed an alloantibody against a red cell antigen they lack, termed Mik. The 3 donors and the renal transplant recipient were crossmatch-compatible with one another. Tube and gel column crossmatch test results were similar. CONCLUSIONS AND CLINICAL IMPORTANCE: The absence of this novel Mik red cell antigen can be associated with naturally occurring anti-Mik alloantibodies and can elicit an acute hemolytic transfusion reaction after an AB-matched blood transfusion.     

Variable rate nitrogen fertilizer response in wheat using remote sensing

Nitrogen (N) fertilizer application can lead to increased crop yields but its use efficiency remains generally low which can cause environmental problems related to nitrate leaching as well as nitrous oxide emissions to the atmosphere. The objectives of this study were to: (i) to demonstrate that properly identified variable rates of N fertilizer lead to higher use efficiency and (ii) to evaluate the capability of high spectral resolution satellite to detect within-field crop N response using vegetation indices. This study evaluated three N fertilizer rates (30, 70, and 90 kg N ha^?1) and their response on durum wheat yield across the field. Fertilizer rates were identified through the adoption of the SALUS crop model, in addition to a spatial and temporal analysis of observed wheat grain yield maps. Hand-held and high spectral resolution satellite remote sensing data were collected before and after a spring side dress fertilizer application with FieldSpec, HandHeld Pro^® and RapidEye?, respectively. Twenty-four vegetation indices were compared to evaluate yield performance. Stable zones within the field were defined by analyzing the spatial stability of crop yield of the previous 5 years (Basso et al. in Eur J Agron 51: 5, 2013). The canopy chlorophyll content index (CCCI) discriminated crop N response with an overall accuracy of 71 %, which allowed assessment of the efficiency of the second N application in a spatial context across each management zone. The CCCI derived from remotely sensed images acquired before and after N fertilization proved useful in understanding the spatial response of crops to N fertilization. Spectral data collected with a handheld radiometer on 100 grid points were used to validate spectral data from remote sensing images in the same locations and to verify the efficacy of the correction algorithms of the raw data. This procedure was presented to demonstrate the accuracy of the satellite data when compared to the handheld data. Variable rate N increased nitrogen use efficiency with differences that can have significant implication to the N₂O emissions, nitrate leaching, and farmer’s profit.     

In vitro validation of a Pitot-based flow meter for the measurement of respiratory volume and flow in large animal anaesthesia

Objective  To remodel and validate commercially available monitors and their Pitot tube-based flow sensors for use in large animals, using in vitro techniques.
Study design  Prospective, in vitro experiment.
Methods  Both the original and the remodelled sensor were studied with a reference flow generator. Measurements were taken of the static flow-pressure relationship and linearity of the flow signal. Sensor airway resistance was calculated. Following recalibration of the host monitor, volumes ranging from 1 to 7 L were generated by a calibration syringe, and bias and precision of spirometric volume was determined. Where manual recalibration was not available, a conversion factor for volume measurement was determined. The influence of gas composition mixture and peak flow on the conversion factor was studied.
Results  Both the original and the remodelled sensor showed similar static flow–pressure relationships and linearity of the flow signal. Mean bias (%) of displayed values compared with the reference volume of 3, 5 and 7 L varied between −0.4% and +2.4%, and this was significantly smaller than that for 1 L (4.8% to +5.0%). Conversion factors for 3, 5 and 7 L were very similar (mean 6.00 ± 0.2, range 5.91–6.06) and were not significantly influenced by the gas mixture used. Increasing peak flow caused a small decrease in the conversion factor. Volume measurement error and conversion factors for inspiration and expiration were close to identity.
Conclusion  The combination of the host monitor with the remodelled flow sensor allowed accurate in vitro measurement of flows and volumes in a range expected during large animal anaesthesia.
Clinical relevance  This combination has potential as a reliable spirometric monitor for use during large animal anaesthesia.