魁北克省多日龄猪接种FLEX系列茵格发(R)猪圆环病毒疫苗预防猪圆环病毒相关疾病(PCVAD)的初步结果

人们认为猪圆环病毒2型(PCV2)是发生断奶仔猪多系统衰竭综合征的一个必要因素.目前断奶仔猪多系统衰竭综合征在欧洲称作猪圆环病毒病(PCVD),在北美称作猪圆环病毒相关疾病(PCVAD).     

Femtosecond phase-coherent two-dimensional spectroscopy

Femtosecond phase-coherent two-dimensional (2D) spectroscopy has been experimentally demonstrated as the direct optical analog of 2D nuclear magnetic resonance. An acousto-optic pulse shaper created a collinear three-pulse sequence with well-controlled and variable interpulse delays and phases,which interacted with a model atomic system of rubidium vapor. The desired nonlinear polarization was selected by phase cycling (coadding experimental results obtained with different interpulse phases). This method may enhance our ability to probe the femtosecond structural dynamics of macromolecules.     

Arbuscular Mycorrhizal Fungal Infectivity in Two Soils as Affected by Atmospheric Phenanthrene Pollution

Arbuscular mycorrhizal fungi (AMF) hold a crucial role in ecosystems because they are involved in nutrient cycling between soil and plants. This work aimed at evaluating the impacts that atmospheric pollution by polycyclic aromatic hydrocarbons may have on infectivity of indigenous AMF in soils. Two agricultural soils (Maconcourt, La Bouzule) were exposed for 2?weeks to ambient air (control, C) or to atmospheric phenanthrene (PHE) deposition (180???g?m^?3 air). After exposure, soils were divided into a top (0?C1?cm) and a bottom (1?C15?cm) layer fraction. AMF infectivities of soils were determined after 2?weeks of atmospheric exposition using leek (Allium porum) as bioassay plant. Atmospheric PHE was mainly recovered in the top layer of soil (500?C1,350???g?kg^?1) of both soils and did not readily diffuse into the depth. Atmospheric contamination led to decreases in AMF infectivities of the top layer in both soils and affected the growth of leeks. Our results not only report evidence that infectivity of indigenous AMF is sensitive to PHE in soils but also emphasize that AMF are primary affected by the soil layer regardless to the pollution level.     

A PCR test to detect the cereal root-knot nematode <Emphasis Type="Italic">Meloidogyne naasi</Emphasis>

The cereal root-knot nematode Meloidogyne naasi can cause serious cereal crop losses. The nematode is also found in agricultural fields where non-host crops are grown. Control of M. naasi can be based on preventing its spread, host resistance and crop management as well as on the design of crop rotation systems. Detection methods are required for these purposes and can also be helpful for inspection services and experimental research. This study describes the development of a simple PCR test that enables the detection of M. naasi. Alignment of sequences of rDNA-ITS fragments of M. naasi and five other Meloidogyne species was used to design the M. naasi specific forward primer N-ITS. Together with the reverse primer R195 M. naasi specific amplification was achieved.