Using Bacillus subtilis E20‐fermented soybean meal as replacement for fish meal in the diet of orange‐spotted grouper (Epinephelus coioides,Hamilton)

The potential of Bacillus subtilis E20‐fermented soybean meal (FSBM) as a partial alternative component of fish meal (FM) in fed diets of orange‐spotted grouper (Epinephelus coioides) was evaluated in this study. An FM‐based diet and seven diets containing 10%, 20% and 30% and 10%, 20%, 30% and 40% of FM replaced by soybean meal (SBM) and FSBM, respectively, were fed to grouper for 84 days to evaluate possible substitution levels of FM by tracking growth performance, digestive enzyme activity and morphological changes in the liver and distal intestine. No significant differences in survival and muscle composition of grouper were found between controls and treatments. Growth performance and feed efficiency of fish fed diets with FM replaced by FSBM up to 30% were not significantly different from controls, whereas significantly decreased growth performance and feed efficiency occurred with diets containing >20% of SBM. Based on the feed efficiency, the maximum substituted levels of FM by SBM and FSBM in grouper diets were 18.36% and 29.32%, respectively, based on broken‐line analyses. Histopathological changes in the liver and distal intestine, and significantly lower activity levels of digestive enzymes, including pepsin in the stomach and trypsin, chymotrypsin, amylase and lipase in the distal intestine, were found in fish fed a diet containing 30% of FM replaced by SBM. However, these parameters were improved by the substitution of FSBM. It is therefore believed that FSBM has great potential to be used as a protein source in grouper diets in partial replacement of FM.     

Immune response of largemouth bass, <Emphasis Type="Italic">Micropterus salmoides</Emphasis>, to whole cells of different <Emphasis Type="Italic">Nocardia seriolae</Emphasis> strains

Largemouth bass Micropterus salmoides were immunized with four different N. seriolae strains—two α-glucosidase-positive (961113, KU040801) and two α-glucosidase-negative (94260, OTTS) strains—along with Freund’s incomplete adjuvant. After primary immunization (week 0), a booster was administered at weeks 4 and 8. Nonspecific immune responses to multiple immunizations with the different N. seriolae strains were determined based on serum lysozyme activity and nitroblue tetrazolium (NBT)-positive cells in peripheral blood. The serum lysozyme activity and NBT-positive cells in peripheral blood were not significantly increased even after the two booster immunizations. Specific antibody responses against N. seriolae cells were investigated by enzyme-linked immunosorbent assay. At 4 weeks after immunization, all groups immunized with N. seriolae antigens showed significant increases in their specific antibody levels. The sera from fish immunized with different N. seriolae strains exhibited reactivity with N. seriolae sonicated antigens of 28, 30, 36 and 84 kDa by western blot analysis. After two boosters, fish were challenged with live N. seriolae to assess the vaccine’s efficacy; however, multiple injections of the N. seriolae strains did not reduce mortality, irrespective of the bacterin.     

Evolutionary implications of two rainbow trout growth hormone genes

The primary structures of two rainbow trout growth hormone mRNAs (GH1 and GH2) have been deduced by direct sequencing of their respective cDNA clones and portions of the mRNA. Both GH1 and GH2 mRNA contain open reading frames comprised of 630 nucleotides and encode 210 amino acid residues of which 11 are variant. The translated regions of both mRNA are flanked by a short but rather conserved 5′-end, and a relatively long but highly diverged 3′-end. The differences at translated and 3′-untranslated regions suggest that the GH1 and GH2 mRNA originate from different loci. The GH1 and GH2 mRNA are likely transcribed from two distinct loci which were duplicated during tetraploidization of salmonid genome between 50 to 100 million years ago. The GH2 gene has been isolated and sequenced from a rainbow trout genomic library. This gene spans a region of approximately 4 kilobases. The trout GH gene is comprised of 6 exons and 5 introns, in contrast to 5 exons and 4 introns in mammals. The additional intron in the trout gene interrupts the translated regions that are analogous to the last exon of the mammalian counterpart. The alleged internally repeating sequences in mammalian GH, prolactin (Pr1) and placental lactogen (PL) are not observed in the predicted polypeptide sequence of trout GH. In addition, direct repeats that flank exons I, III and V of mammalian GH, Pr1 and PL genes are absent in trout gene. These findings indicate that the rainbow trout GH gene structure does not support the current hypothesis that internally repeated regions in GH, Pr1 and PL arose from a small primordial gene.     

中国水稻三化螟防治研究的进展

在中国为害水稻較重的螟虫已知有6种,以三化螟 Tryporyza incertulas (Wlk.)最为重要,分布于我国中南部稻区。本文阐述了气候、食料、水稻栽培制度和生物等因素对三化螟种群数量变动的影响,并指出作为螟虫食料的水稻及其栽培制度的作用更为明显。研究証明,三化螟的产卵、侵入、成活、繁殖和为害都与水稻的生育期有密切关系,水稻的分蘖期及孕穗期,都是水稻最易受害的生育期,在这两个时期被害,会造成枯心或白穗;而秧田期、移植至回青期、圓稈期和成熟期都对螟虫不利。螟虫的发生基数和生活环境条件,密切影响种群数量的变动,而这些都受水稻栽培制度的影响。发生基数决定于春季螟虫的有效虫源,其数量的大小对当年的螟虫,尤其对第一、二代的发生量有密切关系。螟害程度主要决定于:(1)种群数量和(2)水稻最易受害的生育期与螟虫盛发期配合程度的综合作用。为了加強防治,各地区必须因地制宜,利用耕作栽培措施,一方面尽可能消灭虫源、压低发生基数、控制以后各代螟虫的发生;另一方面力求改进栽培技术、調节水稻生育期,恶化螟虫的生活条件,避免或減輕螟害。化学防治也是治螟的一項重要措施。目前广泛应用的药剂是6％丙体六六六,每亩用量在防治枯心时为1.5斤,防治白穗为2斤。主要的施药方法为泼浇和撒毒土,两者对防治枯心的效果都很好;撒毒土防治白穗的效果虽稍差,但操作簡便易行。在螟虫发生期內,适值分蘖和孕穗的水稻田一般都要施药;但預测螟害低于1％的田块,可不防治。防治枯心的施药适期一般在孵化高峯前1—2天天开始,如虫量很大,要提前到盛孵始期用药。防治白穗的施药适期是:在蚁螟盛孵前孕穗的水稻,普通在盛孵始期开始施药;蚁螟盛孵后孕穗的水稻,在孕穗始期开始用药。稻螟是我国长期以来的一种严重害虫,解放前因螟害常年損失稻谷10％以上。解放后,在党和政府的領导下,科学技术有了显著的进展,治螟工作貫彻了“防治并举、以防为主”的方針,“以农业防治为基础,重点使用药剂綜合防治”的策略;采用了准确的預测預报;开展了群众性的防治活动,基本上控制了螟虫的危害,1663年的螟害率已压低到2％左右,不少地区已降低到1％以下。这都是在总路线、大跃进、人民公社三面紅旗光輝照耀下,領导、技术人員、群众三結合所取得的成果的     

Nanosize of zinc oxide and the effects on zinc digestibility,growth performances,immune response and serum parameters of weanling piglets

The aim of this study was to investigate the effect of dietary supplementation of nanosize zinc on zinc digestibility, growth performances, immune response and serum parameters of weanling piglets. Ninety‐six LYD weanling piglets were assigned to control, zinc oxide (ZnO), organic‐Zn (Zn‐methionine) and nanosize ZnO (nano‐Zn) groups with four replicates. The zinc was at the 120 mg/kg level in the treatment group's diet, while the control group's was 80 mg/kg Zn. The experiment results indicated that the nano‐Zn and organic‐Zn groups had significantly higher Zn digestibility compared to the ZnO and control groups. For the immune response traits, the IgG level and goat red blood cells (GRBC) antibody titer were nano‐Zn and organic‐Zn>ZnO>control; in the phytohemagglutinin (PHA) challenge test result, nano‐Zn>organic‐Zn>ZnO>control; in regard to the γ‐globulin level, nano‐Zn and organic‐Zn>ZnO and control, with significant difference between groups. In the serum parameters aspect, serum Zn concentration in nano‐Zn and organic‐Zn groups were higher than in the ZnO and control groups, serum growth hormone concentration was increased in the nano‐Zn group than in the other groups. In conclusion, nanosize zinc oxide for dietary supplementation can increase zinc digestibility, serum growth hormone levels and carbonic anhydrase activity and enhance the immune response of weanling piglets.     

Concentration and Composition of Astaxanthin in Black Tiger Prawn Penaeus monodon Postlarvae Fed Artemia sp. Nauplii or Mauxia Shrimsp Acetes intermedius

Minced Taiwan mauxia shrimp Acetes intermedius , an alternative to brine shrimp Artemia sp. nauplii, has long been used as a principal or supplemental feed in prawn hatcheries in Southeast Asia and India. In this study, black tiger prawn Penaeus monodon postlarvae were fed with frozen brine shrimp nauplii (diet B) or minced Taiwan mauxia shrimp (diet M) for 4 wk to compare their astaxanthin concentration and composition, survival, and growth. Diet B contained two and a half times more total carotenoid (TC) than diet M, with canthaxanthin as a major (79%) carotenoid, but without astaxanthin, a predominant carotenoid in crustaceans. Of its TC in diet M, 55% was β-carotene and 17% astaxanthin. B-prawn (postlarvae fed with diet B) had a similar growth rate as M-prawn and twice the survival rate as M-prawn. The concentrations of total astaxanthin (TA), free astaxanthin (FA), astaxanthin monoester (MA), and astaxanthin di-ester (DA) in B-prawn were all higher than those in M-prawn. Except for FA, no reduction of TA, MA, or DA concentration during the feeding interval was found in B-prawn. However, concentrations of TA, FA, MA, and DA in M-prawn all decreased. TC content of the experimental diets had a greater influence on resulting prawn astaxanthin concentration and composition than carotenoid compositions of the diets.     

Acceleration of post‐mortem changes in Tsaiya duck (Anas platyrhynchos) breast muscle by lactic acid marination

1. The effect of lactic acid marination at 5°C on post mortem changes in breast muscle pectoralis major of spent layer Tsaiya duck was studied.

2. Myofibrils were prepared from 0.1 M and 0.2 M lactic acid marinated muscle and control (non‐marinated samples) sampled at 0, 1, 3, 7 and 14 d post mortem.

3. Changes in myofibril fragmentation index (MFI), myofibrillar proteins and Z‐line structure were examined.

4. Marination of duck breast muscle in lactic acid at 5°C enhanced fragmentation of myofibrils and degradation of myofibrillar proteins and Z‐line structure as compared to control samples.

5. In summary, lactic acid marination at 5°C can accelerate the post mortem degradation of myofibrils in Tsaiya duck breast muscle.     

Detection of race 1 strains of <Emphasis Type="Italic">Ralstonia solanacearum</Emphasis> in field samples in Taiwan using a BIO-PCR method

Bacterial wilt caused by race 1 strains of Ralstonia solanacearum is endemic on tomato produced in diverse agro-ecosystems in Taiwan. Using a new BIO-PCR protocol developed in this study, R. solanacearum was detected in soil, weed, and water samples collected from eight fields with different disease histories and cropping systems located in major tomato production areas. The sensitivity of the BIO-PCR was 1.9 CFU ml⁻¹ and 17 CFU g⁻¹ of soil for pure suspension and infested soil, respectively. The positive detection frequency of the BIO-PCR method was 66.6, 39.6, 23.1, and 31.8% for all tested samples of soil, weed rhizosphere soil, weed root, and water, respectively, and was higher than plating on MSM-1 medium. Detection of R. solanacearum from field soil indicated that spatial distribution of the pathogen in the field was not even regardless of the presence or absence of the disease and the different agro-ecosystems where the sampled fields were located, and the degree of unevenness was higher when tomato was absent from the field. Weed rhizosphere soils could be good sampling targets to monitor the pathogen in the field, because a higher positive detection proportion and population of R. solanacearum were found in the rhizosphere rather than the root of the collected weed samples. Symptomless weeds and contaminated irrigation, standing, or drainage waters were found to be important for the over-season survival and dissemination of R. solanacearum.