Host-feeding patterns of Culex tritaeniorhynchus and Anopheles sinensis (Diptera: Culicidae) in a ricefield agroecosystem.

金沢大学理工研究域　自然システム学系水田発生性蚊類成虫の吸血選択を調べるために, 佐賀県西有田町で1996及び1997年の5月から9月に成虫採集を行った。ドライアイス付加ライトトラップと吸虫管により合計31,804頭のコガタアカイエカとシナハマダラカ雌成虫を採集した。調査したすべての牛舎と豚舎ではライトトラップ採集により多数の成虫が捕獲されたが(牛舎7,933,豚6,441,鶏舎5,267), 鶏舎では吸血蚊がほとんど採集されなかった。コガタアカイエカとシナハマダラカの吸血率は, 牛舎と豚舎ではそれぞれ62%(N=7,113), 74%(N=7,261)であったが, 鶏舎では5%以下(N=5,267)であった。ELISAによる吸血源同定の結果, 両種とも鶏よりも牛と豚を選択していることが示された。また, 牛舎と隣接した鶏舎から採集された吸血蚊も90%以上(N=143)が牛を吸血していた。鶏よりも豚と牛から吸血する傾向は採集場所(棚田周辺か平野部), 採集方法(ライトトラップか吸虫管)を問わず観察された。 Adults of rice-field mosquitoes were collected between May and September of 1996 and 1997 in Nishi Arita, Saga Prefecture, Japan, to determine their feeding pattern in an area where animals were available in large numbers. In total, 31,804 female Culex tritaeniorhynchus and Anopheles sinensis were collected from animal sheds using dry ice-baited light traps and mouth aspiration. Light traps in all the animal sheds captured large numbers of mosquitoes (cowsheds 7,933,pigsties 6,441 and chicken sheds 5,267 mosquitoes), although few fed upon the chickens. Overall, 62% (N=7,113) of fed Cx. triaeniorhynchus and 74% (N=7,261) of An. sinensis were caught by light traps at the cowsheds and pigsties compared to less than 5% (N=5,267) at the chickens sheds. The type of animal in the shed was the most important factor determining the feeding rates. Blood-meal identification by direct ELISA indicated that both Cx. tritaeniorhynchus and An. sinensis preferred cows and pigs to chickens. Over 90% (N=143) of the fed mosquitoes collected from one chicken shed had fed upon cows in an adjoining cowshed. The tendency to feed upon cows and pigs more than on chickens was observed both in the hillside (terraced) and lowland ricefields. This trend is shown in the results obtained by both the aspirator and light trap collection methods

特別養護老人ホームにおける看護の実態調査(その1) : S県の特別養護老人ホームにおける

特別養護老人ホームは、措置制度による運営から介護報酬による経営へ変わり、多くの課題が明らかになってきている。本稿では、特養の医療体制に着目し、施設長・看護職責任者・寮母職責任者を対象に、看護の実態を調査した。その結果、看護業務の現状と今後のあり方については、3者ともに最も多くの人が「医療的業務が主で生活援助が従」と回答した。看護職増員の必要性については、3者ともに半数以上が「必要」と回答した。「理由」は、3者ともに「施設内医療の必要性」をあげた者が8割以上を占めた。看護職の今後のあり方については、医療知識・技術を深め高齢者の健康状態の把握や状態変化への適切な対処ができ他職種と連携でき、介護職への医療技術指導ができることが望まれていることが明らかにされた

Phytochrome mediates the external light signal to repress FT orthologs in photoperiodic flowering of rice

Phytochromes confer the photoperiodic control of flowering in rice (Oryza sativa), a short-day plant. To better understand the molecular mechanisms of day-length recognition, we examined the interaction between phytochrome signals and circadian clocks in photoperiodic-flowering mutants of rice. Monitoring behaviors of circadian clocks revealed that phase setting of circadian clocks is not affected either under short-day (SD) or under long-day (LD) conditions in a phytochrome-deficient mutant that shows an early-flowering phenotype with no photoperiodic response. Non-24-hr-light/dark-cycle experiments revealed that a rice counterpart gene of Arabidopsis CONSTANS (CO), named PHOTOPERIOD SENSITIVITY 1 (Heading date 1) [SE1 (Hd1)], functions as an output of circadian clocks. In addition, the phytochrome deficiency does not affect the diurnal mRNA expression of SE1 upon floral transition. Downstream floral switch genes were further identified with rice orthologs of Arabidopsis FLOWERING LOCUS T (FT). Our RT-PCR data indicate that phytochrome signals repress mRNA expression of FT orthologs, whereas SE1 can function to promote and suppress mRNA expression of the FT orthologs under SD and LD, respectively. This SE1 transcriptional activity may be posttranscriptionally regulated and may depend on the coincidence with Pfr phytochromes. We propose a model to explain how a short-day plant recognizes the day length in photoperiodic flowering

Identification of QTLs for resistance to powdery mildew and SSR markers diagnostic for powdery mildew resistance genes in melon (Cucumis melo L.)

Powdery mildew caused by Podosphaera xanthii is an important foliar disease in melon. To find molecular markers for marker-assisted selection, we constructed a genetic linkage map of melon based on a population of 93 recombinant inbred lines derived from crosses between highly resistant AR 5 and susceptible ‘Earl’s Favourite (Harukei 3)’. The map spans 877 cM and consists of 167 markers, comprising 157 simple sequence repeats (SSRs), 7 sequence characterized amplified region/cleavage amplified polymorphic sequence markers and 3 phenotypic markers segregating into 20 linkage groups. Among them, 37 SSRs and 6 other markers were common to previous maps. Quantitative trait locus (QTL) analysis identified two loci for resistance to powdery mildew. The effects of these QTLs varied depending on strain and plant stage. The percentage of phenotypic variance explained for resistance to the pxA strain was similar between QTLs (R 2 = 22–28%). For resistance to pxB strain, the QTL on linkage group (LG) XII was responsible for much more of the variance (41–46%) than that on LG IIA (12–13%). The QTL on LG IIA was located between two SSR markers. Using an independent population, we demonstrated the effectiveness of these markers. This is the first report of universal and effective markers linked to a gene for powdery mildew resistance in melon.This work was supported by Green Technology Project (grant DM-1607) from the Ministry of Agriculture, Forestry and Fisheries of Japan and by KAKENHI 19580043 from the Ministry of Education, Culture, Sports, Science and Technology.Peer reviewe

Identification of Binding Targets of a Pyrrole-Imidazole Polyamide KR12 in the LS180 Colorectal Cancer Genome.

Pyrrole-imidazole polyamides are versatile DNA minor groove binders and attractive therapeutic options against oncological targets, especially upon functionalization with an alkylating agent such as seco-CBI. These molecules also provide an alternative for oncogenes deemed "undruggable" at the protein level, where the absence of solvent-accessible pockets or structural crevices prevent the formation of protein-inhibitor ligands; nevertheless, the genome-wide effect of pyrrole-imidazole polyamide binding remain largely unclear to-date. Here we propose a next-generation sequencing-based workflow combined with whole genome expression arrays to address such issue using a candidate anti-cancer alkylating agent, KR12, against codon 12 mutant KRAS. Biotinylating KR12 enables the means to identify its genome-wide effects in living cells and possible biological implications via a coupled workflow of enrichment-based sequencing and expression microarrays. The subsequent computational pathway and expression analyses allow the identification of its genomic binding sites, as well as a route to explore a polyamide's possible genome-wide effects. Among the 3,343 KR12 binding sites identified in the human LS180 colorectal cancer genome, the reduction of KR12-bound gene expressions was also observed. Additionally, the coupled microarray-sequencing analysis also revealed some insights about the effect of local chromatin structure on pyrrole-imidazole polyamide, which had not been fully understood to-date. A comparative analysis with KR12 in a different human colorectal cancer genome SW480 also showed agreeable agreements of KR12 binding affecting gene expressions. Combination of these analyses thus suggested the possibility of applying this approach to other pyrrole-imidazole polyamides to reveal further biological details about the effect of polyamide binding in a genome

Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer

Harlequin ichthyosis (HI) is a devastating skin disorder with an unknown underlying cause. Abnormal keratinocyte lamellar granules (LGs) are a hallmark of HI skin. ABCA12 is a member of the ATP-binding cassette transporter family, and members of the ABCA subfamily are known to have closely related functions as lipid transporters. ABCA3 is involved in lipid secretion via LGs from alveolar type II cells, and missense mutations in ABCA12 have been reported to cause lamellar ichthyosis type 2, a milder form of ichthyosis. Therefore, we hypothesized that HI might be caused by mutations that lead to serious ABCA12 defects. We identify 5 distinct ABCA12 mutations, either in a compound heterozygous or homozygous state, in patients from 4 HI families. All the mutations resulted in truncation or deletion of highly conserved regions of ABCA12. Immunoelectron microscopy revealed that ABCA12 localized to LGs in normal epidermal keratinocytes. We confirmed that ABCA12 defects cause congested lipid secretion in cultured HI keratinocytes and succeeded in obtaining the recovery of LG lipid secretion after corrective gene transfer of ABCA12. We concluded that ABCA12 works as an epidermal keratinocyte lipid transporter and that defective ABCA12 results in a loss of the skin lipid barrier, leading to HI. Our findings not only allow DNA-based early prenatal diagnosis but also suggest the possibility of gene therapy for HI