Origin of the diclidophorid monogenean Neoheterobothrium hirame Ogawa, 1999, the causative agent of anemia in olive flounder Paralichthys olivaceus

In the mid-1990s, Neoheterobothrium hirame suddenly appeared as a new species in olive flounder Paralichthys olivaceus in Japanese coastal waters. Anemia caused by the parasite has prevailed in wild and cultured populations of olive flounder since that time. In this study, to clarify the origin of N. hirame, two Neoheterobothrium species, namely unidentified Neoheterobothrium species (tentatively abbreviated as Neoheterobothrium sp. PL) and N. affine, were collected from Paralichthys lethostigma and Paralichthys dentatus, respectively, off the east coast of North America and compared with N. hirame collected in Japan. No substantial differences were detected in the morphology and DNA sequences of ITS1-5.8S rRNA-ITS2 and mitochondrial cytochrome oxidase subunit I (mt COI) regions between N. hirame and Neoheterobothrium sp. PL. On the other hand, the congeneric N. affine was clearly distinguished from both N. hirame and Neoheterobothrium sp. PL in its longer isthmus and the DNA sequences in ITS1 and mt COI. The absence of differences between N. hirame and Neoheterobothrium sp. PL and the clear difference between both of these and N. affine indicate that N. hirame is conspecific with Neoheterobothrium sp. PL infecting P. lethostigma and that N. hirame was recently introduced from North America to Japan.     

Factors determining the distribution of a keystone understory taxon, dwarf bamboo of the section Crassinodi, on a national scale: application to impact assessment of climate change in Japan

The objective of this study was to identify climatic factors determining the distribution of a keystone understory taxon, section Crassinodi of the genus Sasa, and assess the impacts of climate change on the taxon. Relationships between the distribution of sect. Crassinodi and five climatic variables were explored using classification tree analysis. Potential habitats under current climate and future climate in 2081–2100 were predicted. Potential habitats were further divided into suitable and marginal habitats. The predictive accuracy of the model was assessed using receiver operating characteristic analysis and by comparing model predictions with an independent dataset. The model was reasonably accurate. It showed that the warmth index (WI) and snow cover were the most important climatic variables for Crassinodi distribution. Potential habitats were limited to cooler regions with WI <102.7°C month. Suitable habitats were limited to even cooler regions with WI <84.8°C month. The model also showed that areas with deeper snow than previously reported would provide suitable habitats for Crassinodi under some climatic conditions. In 2081–2100, 37.4% of current potential habitats are predicted to become non-habitats because of increases in WI. Most currently suitable habitats are predicted to vanish from western Japan by 2081–2100. Meanwhile, Hokkaido and high-elevation areas of eastern Honshu will sustain suitable habitats. Sect. Crassinodi, which is adapted to less snowy climates, is predicted to be more affected by climate change than sect. Sasa and Macrochlamys, which are adapted to snowy climates.     

In vitro infection of fractionated chicken lymphocytes by infectious bursal disease virus

Lymphocytes from bursa of Fabricius and thymus of chickens were purified and separated into the three cell subsets--T, B, and null cells--by the techniques of nylon fiber columns and cytotoxicity tests. The in vitro susceptibility of the fractionated lymphocytes to a virulent strain of infectious bursal disease virus (IBDV) was studied by using immunofluorescence as the infection criterion. B cells were highly susceptible. By contrast, T cells and null cells were insusceptible to infection by IBDV. The relationship between the target cells for virus infection and those B cells that possessed surface immunoglobulin (SIg) was tested. B cells were further divided into SIg(M)- and SIg(G)-bearing cells by immunoadsorbent columns employing anti-immunoglobulin M(IgM) (mu-specific) or anti-IgG (gamma-specific) sera coated with Sephadex. The SIg(M)-bearing cells were highly susceptible. These results suggest strongly that SIg(M)-bearing B cells were the target cells for infection by IBDV.     

Sequential changes in the number of surface immunoglobulin-bearing B lymphocytes in infectious bursal disease virus-infected chickens

Variations of B lymphocytes bearing surface immunoglobulin (SIg) M [SIg(M)] and G [SIg(G)] were studied in the spleen and peripheral blood of chickens infected with infectious bursal disease virus (IBDV). The proportion of SIg-bearing B lymphocytes and SIg(M)- and SIg(G)-bearing B cells in chickens infected at one day of age decreased from 1 week postinfection (p.i.) onward and was significantly lower at 8 weeks p.i. In chickens infected at 4 weeks, the percentage of SIg-bearing B cells decreased severely during the first 2 weeks p.i. The decrease of SIg(M)-bearing B cells preceded that of SIg (G)-bearing B cells: the lowest percentage of SIg(M)-bearing B cells has observed 2 to 3 days p.i., and that of SIg(G)-bearing B cells was seen 4 days p.i. The results suggest that SIg(M)-bearing B cells are the major target for IBDV infection.     

Attachment and infection to MA104 cells of avian rotaviruses require the presence of sialic acid on the cell surface

To determine the characters of receptors on target cells for avian rotaviruses, the receptors on MA104 cells for the pigeon rotavirus PO-13, the turkey rotaviruses Ty-1 and Ty-3, and the chicken rotavirus Ch-1 were analyzed. Pretreatment of MA104 cells with neuraminidase greatly reduced the infection by all of the four avian rotavirus strains. Binding of the cell-attachment protein, purified VP8 expressed in bacteria, of strain PO-13 to MA104 cells was also inhibited by pretreatment of cells with neuraminidase. These findings suggest that avian rotaviruses primarily utilize sialic acid-containing molecules as receptors on MA 104 cells.     

Nested PCR检测狂犬病病毒方法的建立及病毒在小鼠体内的移行动态

应用建立的Nested PCR特异地检出狂犬病病毒株CVC、HEP-Flury、ERA、RC-HL、1008、Komatsug-awa的RNA,但对类狂犬病病毒Lagos bat、Duvenhage、Mokola及水泡性口膜炎病毒、轮状病毒、犬瘟热病毒均为阴性。该法敏感性很高,能检出3 TCID50或0.8pg的狂犬病病毒RNA。用该法测定了小鼠脑内感染CVS株后的病毒增殖和移行动态,对感染小鼠的主要内脏器官进行了病毒RNA检测,结果发现小鼠脑内感染CVS 5 d以后在其心、肝、脾、肺等内脏器官均检出了病毒RNA。