Soft rot of root chicory in Hokkaido and its causal bacteria

In August 2010, bacterial soft rot was found on root chicory (Cichorium intybus var. sativum) in Hokkaido, Japan. Severely infected plants in fields were discolored, had wilted foliage, and black necrosis of petioles near the crown. Wilted leaves subsequently collapsed and died, forming a dry, brown or black rosette. The root and crown became partially or wholly soft-rotted. Slimy masses on infected areas of roots, turned dark brown or black. Gram-negative, rod-shaped, peritrichously flagellated, facultatively anaerobic bacteria were exclusively isolated from rotted roots, and typical symptoms were reproduced after inoculation with the strains. The bacteria were identified as Dickeya dianthicola, Pectobacterium carotovorum subsp. carotovorum, and Pectobacterium carotovorum subsp. odoriferum based on further bacteriological characterization and the sequence analysis of the malate dehydrogenase gene and 16S rRNA gene. These bacteria should be included with the previously reported Dickeya (=Erwinia) chrysanthemi in Saitama Prefecture, Japan, as causal pathogens of bacterial wilt of chicory.     

<Emphasis Type="Italic">Agrobacterium tumefaciens</Emphasis>-mediated transformation as a tool for random mutagenesis of <Emphasis Type="Italic">Colletotrichum trifolii</Emphasis>

We transformed Colletotrichum trifolii, the causal agent of alfalfa anthracnose, using Agrobacterium tumefaciens as a new tool for random insertional mutagenesis. Fungal spores of C. trifolii were transformed with T-DNA including the hygromycin phosphotransferase gene (hph). Southern analysis showed that every randomly selected transformant had a unique hybridization pattern of T-DNA, suggesting that the T-DNA was randomly integrated into the fungal genome. More significantly, about 75% of transformants had a single copy of the T-DNA. The results demonstrate that insertional mutagenesis via A. tumefaciens is a useful tool for studying the function of C. trifolii genes.     

Trophic sources and linkages to support mesozooplankton community in the Kuroshio of the East China Sea

Many migratory fishes reproduce and recruit around the Kuroshio, and their survival of early life stages is supported by mesozooplankton. Mesozooplankton standing stocks and productivity equivalent to those on the continental shelf have been found in the Kuroshio; however, there is limited information on trophic sources and linkages to support the mesozooplankton community. Here, we evaluate mesozooplankton feeding on protists and their trophodynamics importance by removal bottle experiments in the Kuroshio of the East China (ECS‐Kuroshio). Pico‐ and nano‐autotrophs dominated chlorophyll a concentrations throughout the study sites across the continental shelf, within the Kuroshio path and in adjacent waters. Calanoid and poecilostomatoid copepods comprised more than 85% of mesozooplankton biomass. Significant mesozooplankton ingestion rates were found for nano‐autotrophs based on size‐fractionated chlorophyll; for haptophytes, chrysophytes, chlorophytes, and diatoms from pigment‐based phytoplankton analysis; and for naked ciliates in the microzooplankton. Based on the estimates of individual carbon budgets, nano‐autotrophs and naked ciliates ingested by mesozooplankton composed 39% of their food requirements, suggesting other available prey like nano‐heterotrophs. These results imply that mesozooplankton ingestion in the ECS‐Kuroshio has great impacts on protozoan and phytoplankton communities and their major trophic pathways are from nano‐sized auto‐ and heterotrophs and ciliates to copepods.     

Mercury distribution in target organs and biochemical responses after subchronic and trophic exposure to Neotropical fish Hoplias malabaricus

In the present study, we investigated the mercury distribution, mercury bioaccumulation, and oxidative parameters in the Neotropical fish Hoplias malabaricus after trophic exposure. Forty-three individuals were distributed into three groups (two exposed and one control) and trophically exposed to fourteen doses of methylmercury each 5 days, totalizing the doses of 1.05 μg g^?1 (M1.05) and 10.5 μg g^?1 (M10.5 group). Autometallography technique revealed the presence of mercury in the intestinal epithelia, hepatocytes, and renal tubule cells. Mercury distribution was dose-dependent in the three organs: intestine, liver, and kidney. Reduced glutathione concentration, glutathione peroxidase, catalase, and glutathione S-transferase significantly decreased in the liver of M1.05, but glutathione reductase increased and lipid peroxidation levels were not altered. In the M10.5, most biomarkers were not altered; only catalase activity decreased. Hepatic and muscle mercury bioaccumulation was dose-dependent, but was not influenced by fish sex. The mercury localization and bioaccumulation corroborates some histopathological findings in this fish species (previously verified by Mela et al. in Ecotoxicol Environ Saf 68:426–435, 2007). However, the results of redox biomarkers did not explain histopathological findings previously reported in M10.5. Thus, fish accommodation to the stressor may reestablish antioxidant status at the highest dose, but not avoid cell injury.     

Differences in the biochemical compositions of two dietary jellyfish species and their effects on the growth and survival of Ibacus novemdentatus phyllosomas

Phyllosomas (planktonic larvae) of slipper lobsters cling onto and feed on jellyfish under both natural and laboratory conditions. Phyllosomas of Ibacus novemdentatus are capable of feeding on various jellyfish species including venomous stingers; however, the range of jellyfish species capable of supporting the growth and survival of phyllosomas is unknown. Seventeen (12 for the first and five for the second trials) and 18 (13 for the first and five for the second trials) phyllosomas were fed exclusively on the jellyfish Aurelia aurita and Chrysaora pacifica, respectively. Aurelia aurita‐fed phyllosomas metamorphosed into the nisto stage (postbenthic larvae) ～54 days after hatching, whereas C. pacifica‐fed phyllosomas did not. Major nutritional compositions such as amino acids, fatty acids and minerals were compared between the two jellyfish species. The proportion of each major nutritional component was not significantly different between the two jellyfish species, suggesting that C. pacifica was not nutritionally inferior to A. aurita. Therefore, the observation that the C. pacifica‐fed phyllosomas did not metamorphose into the nisto stage was not because of major nutritional compositions but due to other factors such as the lack or excess of other minor nutrients, or the species‐specific texture of the jellyfish.     

Improvement of anemia associated with chronic renal failure by recombinant human erythropoietin treatment in ICR-derived glomerulonephritis (ICGN) mice

The ICR-derived glomerulonephritis (ICGN) mouse, a novel inbred mouse strain with a hereditary nephrotic syndrome, develops severe anemia associated with chronic renal failure. To reveal the pathogenic mechanism of anemia in ICGN mice, we subcutaneously administered recombinant human erythropoietin (rhEPO; 5 IU/mouse/day) or saline for 5 days to ICGN mice. In terminal-stage ICGN mice with severe anemia, rhEPO significantly increased hematocrit (Ht), red blood cells (RBC) and hemoglobin levels. Endogenous EPO levels in peripheral blood were reduced by rhEPO injection. No histopathological changes in bone marrow and kidneys were induced by rhEPO injection. Insufficiency of EPO may cause anemia in ICGN mice.     

Effect of anti-ganglioside antibody in experimental Trypanosoma brucei infection in mice

The effect of antibody against ganglioside antigen on Trypanosoma brucei parasites was examined in vitro and in vivo using anti-ganglioside GM1 (AGM-1) monoclonal antibody. The antibody showed complement-dependent cytotoxicity against T. brucei with mouse complement. Furthermore, mice given AGM-1 were challenged intraperitoneally with T. brucei. Although all non-treated control mice died within six days after infection, all of AGM-1-injected mice had survived by six days post-infection. These data suggest that antibody against ganglioside antigen on T. brucei has potential in protection against T. brucei infection.     

CEP peptide induces susceptibility of Arabidopsis thaliana to non-adapted pathogens

CEP peptide was synthesized and tested for induction of disease susceptibility using Arabidopsis Col-0. When Colletotrichum tropicale was used as a non-adapted fungal pathogen, the conidia germinated to form hyphal-like structures, which successfully penetrated epidermis, eventually causing disease symptoms. In such case, PEN2-, but not PEN3-dependent resistance was likely suppressed by CEP peptide. Similarly, the CEP peptide-mediated disease susceptibility was also effective to a non-adapted bacterial pathogen. Notably, such induced susceptibility was also evident on Arabidopsis mutants lacking the previously identified receptors, suggesting that the CEP peptide modulates Arabidopsis immunity through an unidentified receptor(s).