Influence of Siphonophore Behavior upon Their Natural Diets: Evidence for Aggressive Mimicry

Collection by divers permitted determination of the natural diets of siphonophore species within II genera. Siphonophores that swim rapidly to spread their tentacles capture small prey, whereas those that swim very weakly capture much larger prey. Nematocyst batteries of two species of weak swimmers closely resemble copepods and fish larvae. Morphology, behavior, and diet suggest that these two species attract large prey by mimicking other zooplankton.     

Use of a multifenestrated indwelling lavage system for treatment of septic digital teno-synovitis in cattle

Septic tenosynovitis was diagnosed in seven cattle on the basis of history, physical examination, radiographs, cytological examination of tendon sheath fluids, and microbial culture. A commercially available indwelling multifenestrated silicone rubber drain was used to perform frequent lavage of the flexor tendon sheaths. The sepsis resolved in all cattle. Five of six cattle for which long-term (> 1 year) follow-up information was available were clinically sound on the affected limb and had remained productive members of the herd.     

The outcome of acute hepatitis C predicted by the evolution of the viral quasispecies

The mechanisms by which hepatitis C virus (HCV) induces chronic infection in the vast majority of infected individuals are unknown. Sequences within the HCV E1 and E2 envelope genes were analyzed during the acute phase of hepatitis C in 12 patients with different clinical outcomes. Acute resolving hepatitis was associated with relative evolutionary stasis of the heterogeneous viral population (quasispecies), whereas progressing hepatitis correlated with genetic evolution of HCV. Consistent with the hypothesis of selective pressure by the host immune system, the sequence changes occurred almost exclusively within the hypervariable region 1 of the E2 gene and were temporally correlated with antibody seroconversion. These data indicate that the evolutionary dynamics of the HCV quasispecies during the acute phase of hepatitis C predict whether the infection will resolve or become chronic.     

Hydration of macromolecules

Frozen protein and nucleic acid solutions at -35 degrees C show relatively narrow (100 milligauss) proton nuclear magnetic resonance signals which are assignable to water that is sufficiently mobile to reduce the dipolar broadening normally associated with solids. Hydration was found to be 0.3 to 0.5 gram of water per gram of protein. Nucleic acids are three to five times as hydrated as proteins. Conformational changes in solution produce detectable changes in linewidth or amount of "bound" water, or both. The very fact that the water signals can be observed by high resolution nuclear magnetic resonance suggests that it is not "ice-like" in any literal sense, although it is clearly less mobile than liquid water at the same temperature. A simple model is described which considers both surface hydration and trapped water.     

Drought and nitrogen source effects on nitrogen nutrition,seed growth,and yield in soybean

Drought in soybean [Glycine max (L.) Merr.] decreases yield‐related processes and N₂ fixation is more sensitive to drought than are many other of these processes. Therefore, application of nitrogen (N) fertilizer may increase drought tolerance over those plants primarily dependent on N₂ fixation. In a field experiment, NH₄NO₃ applications (+N) to drought‐stressed soybean resulted in biomass and N accumulation rates similar to those rates for an irrigated treatment without N fertilizer (‐N). In contrast, biomass and N accumulation rates were decreased for the ‐N treatment. N fertilization increased seed growth rate and decreased seed fill duration for irrigated and drought treatments. In the drought treatment, N application increased seed number per unit area, which resulted in higher yields. In a greenhouse experiment, fertilization with either KN0₃ or NH₄C1 increased biomass and N accumulation rates during drought over those of plants dependent solely on N₂ fixation. It was concluded that application of N fertilizer to soybean increases drought tolerance because of the extreme sensitivity of N₂ fixation to drought.     

An assay for circulating antibodies to a major etiologic virus of human non-A, non-B hepatitis

A specific assay has been developed for a blood-borne non-A, non-B hepatitis (NANBH) virus in which a polypeptide synthesized in recombinant yeast clones of the hepatitis C virus (HCV) is used to capture circulating viral antibodies. HCV antibodies were detected in six of seven human sera that were shown previously to transmit NANBH to chimpanzees. Assays of ten blood transfusions in the United States that resulted in chronic NANBH revealed that there was at least one positive blood donor in nine of these cases and that all ten recipients seroconverted during their illnesses. About 80 percent of chronic, post-transfusion NANBH (PT-NANBH) patients from Italy and Japan had circulating HCV antibody; a much lower frequency (15 percent) was observed in acute, resolving infections. In addition, 58 percent of NANBH patients from the United States with no identifiable source of parenteral exposure to the virus were also positive for HCV antibody. These data indicate that HCV is a major cause of NANBH throughout the world.     

Quantitative Polymerase Chain Reaction (PCR) for Detection of Aquatic Animal Pathogens in a Diagnostic Laboratory Setting

Abstract

Real-time, or quantitative, polymerase chain reaction (qPCR) is quickly supplanting other molecular methods for detecting the nucleic acids of human and other animal pathogens owing to the speed and robustness of the technology. As the aquatic animal health community moves toward implementing national diagnostic testing schemes, it will need to evaluate how qPCR technology should be employed. This review outlines the basic principles of qPCR technology, considerations for assay development, standards and controls, assay performance, diagnostic validation, implementation in the diagnostic laboratory, and quality assurance and control measures. These factors are fundamental for ensuring the validity of qPCR assay results obtained in the diagnostic laboratory setting.

Received March 30, 2011; accepted May 6, 2011