两种树叶在华南地区陆地与水环境中的分解速率比较

利用粗细2种孔径的分解袋对两种树叶(蒲桃和白兰)在广州长岗山自然保护小区的陆地和池塘中分别进行了为期210d和60d的分解研究.在陆地环境中,蒲桃在粗细网袋中的分解速率分别为0.003318d^-1和0.003728d^-1,白兰在粗细网袋中的分解速率分别为0.009238d^-1和0.004379d^-1;在静水环境中,蒲桃在粗细网袋中的分解速率分别为0.009536d^-1和0.012591d^-1,白兰在粗细网袋中的分解速率分别为0.017949d^-1和0.020759d^-1.结果表明,两种树叶在陆地中的分解速率均慢于水环境.另外,由于富含丹宁的蒲桃叶片具有抑菌作用,因此,无论在陆地还是水环境,蒲桃树叶的分解速率均慢于白兰树叶.     

Genetic relationship among species in the genus Sonneratia in China as revealed by inter-simple sequence repeat (ISSR) markers

Inter-simple sequence repeat (ISSR) analysis was used to establish the genetic relationship among six Sonneratia species in China. A total of 100 primers were screened, of which 11 polymorphic and informative patterns were selected to determine the genetic relationship. Four hundred and eighty five DNA bands were amplified, among which 481 bands (99.18%) were polymorphic. The average number of DNA bands amplified by each primer was 44. Similarity coefficients were calculated and a dendrogram was constructed by using UPGMA algorithm. The six Sonneratia species were divided into two major groups. Group I consisted of Sonneratia caseolaris, Sonneratia × gulngai, Sonneratia alba, and Group II included Sonneratia × hainanensis, Sonneratia ovata and Sonneratia apetala. In Group I, S. × gulngai was close to S. alba, and in Group II, S. × hainanensis was close to S. ovata. The genetic relationships estimated by the polymorphism of ISSR markers are basically in agreement with those previously inferred by morphological data. Thus, ISSR approach is a reliable marker system that can be used to study genetic relationship in the genus Sonneratia.     

植物提取物和药剂对蔬菜蚜虫种群的联合控制作用

研究白蝴蝶(Syngonium podophyllum)乙醇提取物、苍耳(Xanthium sibiricum)乙醇提取物、机油乳剂和0.3%印楝素乳油对桃蚜(Myzus persicae)和萝卜蚜(Lipaphis erysimi)的控制效果.室内四因子(1/2实施)二次正交回归旋转组合设计测试对有翅蚜的忌避作用,结果表明,对有翅桃蚜的主要忌避作用物为苍耳乙醇提取物,当苍耳提取物与白蝴蝶乙醇提取物混用,以及机油乳剂和印楝素混用时,对桃蚜有翅蚜的忌避效果提高;而对萝卜蚜有翅蚜的忌避作用主要受苍耳提取物和白蝴蝶提取物的影响.这些干扰作用均是非线性的.田间试验结果,单独使用白蝴蝶提取物对有翅成蚜有较强的驱避作用;对萝卜蚜自然种群的干扰控制作用以4种植物提取物和药剂混配效果最好,达95.7%;对桃蚜自然种群干扰控制效果最好的则是白蝴蝶提取物,控制效果达87%;同时,白蝴蝶提取物与印楝素乳油混配以及苍耳提取物与印楝素乳油混配,对两种蚜虫的控制效果均达80%以上.     

Occurrence of pyrrolizidine alkaloids in three Ethiopian Solanecio species

Three Ethiopian Solanecio species, namely Solanecio angulatus (Vahl) C. Jeffrey, Solanecio mannii (Hook. f.) C. Jeffrey, and Solanecio tuberosus (Sch. Bip. ex A. Rich.) C. Jeffrey var. tuberosus were analysed by capillary gas chromatography–mass spectrometry (GLS–MS) for their pyrrolizidine alkaloid content. All the extracts investigated contain pyrrolizidine alkaloids. Whilst only traces of alkaloids could be detected in the leaf extract of S. angulatus, the content of alkaloids in the other samples ranged between 0.13% dry weight (for the flowers of S. angulatus) and 0.58% (for the tubers of S. tuberosus). Altogether 17 alkaloids were detected out of which 14 were unambiguously identified by comparing their retention indices, molecular masses and mass fragmentation patterns with defined reference data from PAs database or in some cases with reference compounds. The hepatotoxic macrocyclic diesters senecionine and retrosine figured as major alkaloids in the flowers of S. angulatus, whereas the platynecine type alkaloid, 7-O-senecioylplatynecine occurred in higher amount than the other alkaloids detected in the leaves of S. mannii. The tuberous annual herb, S. tuberosus contains eruciflorine as a major alkaloid in the leaves, flowers and tubers. Senecionine figures as one of the major components of the tubers of S. tuberosus. To the best of our knowledge this is the first published report on the occurrence of pyrrolizidine alkaloids in the genus Solanecio. In addition to the chemotaxonomic significance of the detected alkaloids, a brief remark is made on the findings in the light of the use of these plants as medicinal herbs and/or as nectar or pollen source for the production of honey.     

Phylogenetic identification of Sparganum proliferum as a pseudophyllidean cestode

Sparganum proliferum is characterized by continuous branching and budding, the resulting progeny invading all tissues of the human body, causing fatal sparganosis. Its life cycle, definitive hosts and the route of infection to humans have not yet been disclosed. Because its morphology is similar to Spirometra erinacei, the phylogeny of S. proliferum has been thought to be identical to or closely related to S. erinacei. However, the taxonomy of S. proliferum has not been established up to present due to the lack of definitive observations. In order to clarify the phylogenetic relationship between S. proliferum and S. erinacei, nucleotide sequences of mitochondrial NADH dehydrogenase subunit 3 gene (ND3) and four mitochondrial tRNA coding genes of S. proliferum and other pseudophyllidean cestodes were analyzed. The sequences of S. proliferum showed high similarity to those of S. erinacei, although they were clearly different from each other, indicating that the phylogeny of S. proliferum and S. erinacei is distinct. This is the first report showing the phylogenetic relationship among S. proliferum and other pseudophyllidean cestodes at the DNA sequence level.     

增温和升高CO2浓度对桑树幼苗的生长和叶片品质的影响

研究了增温(+2 ℃)、升高CO₂浓度(+300 ppm)及同时增温和升高CO₂浓度(+2 ℃和+300 ppm CO₂)处理60 d后1年生桑树幼苗的形态、生物量积累及叶片品质的变化.结果表明: 与对照相比,增温显著增加桑树的基径、叶片数、总叶面积、叶干质量、叶干质量分数和可溶性蛋白含量,分别增加了9.9%、17.4%、23.0%、9.2%、10.1%和23.1%;升高CO₂浓度显著增加了桑树幼苗的茎干质量、根干质量和总干质量,比对照分别增加10.7%、15.9%和9.2%,但对幼苗的形态和叶片品质无显著影响;同时增温和升高CO₂浓度条件下,叶片数、株高、基径、总叶面积、叶干质量、根干质量、总干质量、叶片可溶性糖和粗蛋白含量均显著升高,与对照相比分别增加28.8%、9.1%、19.4%、32.6%、12.4%、17.2%、10.1%、45.8%和11.9%,但粗纤维含量显著降低16.8%.短期增温和升高CO₂浓度对桑树幼苗的生长发育和叶片品质有促进作用.     

重组质粒pcDNA3-dnaJ/蛋白DnaJ异源免疫诱导Th1和Th17细胞免疫应答抵抗肺炎链球菌感染 *

目的 探索更有效的肺炎链球菌DNA疫苗和疫苗免疫策略,并探究其中的保护机制。方法 构建重组质粒pcDNA3-dnaJ并表达DnaJ蛋白,实验分别设置重组质粒pcDNA3-dnaJ/蛋白DnaJ免疫小鼠组及单独质粒pcDNA3-dnaJ免疫小鼠组,分别比较肺炎链球菌菌株攻毒后小鼠鼻腔灌洗液细菌载量及生存率,采用ELISA检测免疫小鼠血清抗体效价及炎症因子,流式细胞术分析体外BMDCs激活情况及Th1和Th17细胞免疫应答。结果 质粒pcDNA3-dnaJ免疫3次可诱导血清中抗原特异性抗体的产生,并减少肺炎链球菌攻毒后鼻咽部的细菌载量,但在防止致死性感染方面效果较差。然而,与重复质粒DNA接种三次相比,pcDNA3-dnaJ 1次/ DnaJ蛋白加强1次的免疫策略可以显著减少鼻咽中的肺炎链球菌定植,并能够更好的预防致死性感染。此外,与DNA质粒加强免疫相比,DnaJ蛋白加强免疫后可产生更高水平的IFN-γ和IL-17A。结论 重组质粒pcDNA3-dnaJ/蛋白DnaJ异源免疫可能通过活化树突状细胞,进而诱导Th1和Th17细胞免疫应答,抵抗肺炎链球菌感染。     

Application of lat gene disruption to increase the clavulanic acid production of Streptomyces clavuligerus

A 1.7 kb fragment of lat was obtained from Streptomyces clavuligerus NRRL 3585, and recombinant plasmid pKC1139-lat, which was used to disrupt the lat gene was constructed. pKC1139-lat was introduced into S. clavuligerus by bi-parental conjugation from Escherichia coli ET12567 to S. clavuligerus. The apramcin-resistant transformants were obtained and through homogeneous single-crossover between recombinant plasmid pKC1139-lat and the S. clavuligerus chromosome lat disrupted mutant strains were obtained. The genome of S. clavuligerus NRRL 3585 and the lat disrupted mutants were analyzed by PCR technique, the bioactivity of cephamycin C in the two kinds of strains were also tested. Both results proved that lat was disrupted by the insertion of pKC1139 in the lat disrupted mutants. And the production of clavulanic acid of these two kinds of strains were analyzed by HPLC with different incubation time interval (96 and 120 h), and the yield in the lat mutants was approximately 2.6 fold higher at their highest production point.     

The Aspergillus niger carbon catabolite repressor encoding gene, creA

In order to undertake a comparative analysis of carbon catabolite repression in two Aspergillus species, the creA gene has been isolated from A. niger by cross hybridization, using the cloned A. nidulans gene. The A. niger gene has been shown to be functional in A. nidulans by heterologous complementation of the creA204 mutation of A. nidulans. Overall, the genes show 90% sequence similarity (82% identity) at the amino acid (aa) level. There were some striking similarities between the aa sequences encoded by the two fungal creA genes and two genes involved in carbon catabolite repression in Saccharomyces cerevisiae. The zinc-finger regions showed 96% similarity (84% identity) with the zinc-finger region of the MIG1 gene of S. cerevisiae. The CREA protein contains a stretch of 42 aa that is identical in A. niger and A. nidulans, and these show 81% similarity (33% identity) with a region of the S. cerevisiae RGR1 gene.     

Millardia meltada, a new host for Acanthocheilonema viteae and a simple technique for separation of microfilariae from peripheral blood

, and 1992. Millardia meltada, a new host for Acanthocheilonema viteae and a simple technique for separation of microfilariae from peripheral blood. International Journal for Parasitology 22: 1165–1168. Millardia meltada were infected with Acanthocheilonema viteae and examined for their susceptibility. The morbidity of infected M. meltada was low compared with that of jirds. On day 47 post-infection (p.i.), 13 of 14 M. meltada developed microfilaremia. Male M. meltada then showed gradually increasing microfilaremia with a peak level of 7000 per 30 μl blood at week 20 p.i., which was much higher than that (3000) of male jirds. In contrast, microfilarial densities of female M. meltada were markedly low with a peak level of 200 during weeks 10–12 p.i. A simple centrifugation technique with Lympholyte-M was devised for microfilarial separation from the peripheral blood of infected M. meltada and yielded approximately 17 × 10⁵ viable microfilariae from 1 ml of blood. This method also makes it possible to collect microfilariae from the same individuals repeatedly. M. meltada, coupled with this microfilarial separation technique, serves as a useful animal model for microfilarial studies of A. viteae.     

The Mycobacterium tuberculosis mysB gene product is a functional equivalent of the Escherichia coli sigma factor, KatF

Mycobacterium tuberculosis, the causative agent of tuberculosis, may remain dormant within its host for many years. The nature of this dormant or latent state is not known, but it may be a specialized form of the stationary growth phase. In Escherichia coli, KatF (or RpoS) is the major stationary phase sigma factor regulating an array of genes expressed in this phase of growth. A potential M. tuberculosis katF homologue was cloned using a fragment of the E. coli katF gene as a probe. DNA sequence analysis of a resultant clone showed 100% identity to a fragment of DNA encoding the M. tuberculosis mysA and mysB genes. Overexpression of mysB in M. bovis BCG resulted in an increase in katG mRNA and catalase and peroxidase activity, and an increase in sensitivity of the cells to isoniazid. An increase in katG promoter activity from a reporter vector was demonstrated when mysB was overexpressed from the same plasmid, indicating a direct relationship between MysB and katG expression.     

Biosystematics and genetic relationships of Solea aegyptiaca and S. senegalensis

The isoenzymes from seven populations of Solea senegalensis or aegyptiaca were compared et 24–30 loci, six of which display significant differences in their allelic frequencies. In addition, these populations were compared to six other Soleidae species, namely Solea vulgaris, S. impar, S. lascaris, S. lutea, Michrochirus azevia, and M. variegatus. It was shown that S. senegalensis and S. aegyptiaca can be separated into two distinct genetic groups. Their high genetic similarity in comparison with the other species of Soleidae studied suggests that they have a common origin. The systematic status (species or semispecies) of these taxa could not, however, be elucidated. The high degree of genetic polymorphism observed in the regions where the two taxe are found together suggests that there still is some gene flow between them. However, this could be due to selection.     

Hfr-mediated conjugative transfer of pBR322 vector carrying the chromosomal DNA of Escherichia coli

Hybrid plasmids consisting of a non-mobilized plasmid, pBR322, and a segment of chromosomal DNA of Escherichia coli could be transferred from an Hfr donor to recipient cells by a bacterial mating. When the chromosomal DNA in the plasmid corresponded to the early transfer region of the Hfr, the frequency of the transfer was high. The recA function of both donor and recipient cells was required in the transfer. The physical association of the hybrid plasmid with the transferring Hfr chromosome through the homologous sequences may mediate the transfer of the non-mobilized plasmid. This phenomenon is useful for the determination of the chromosomal location of an unidentified fragment cloned in a non-mobilized plasmid.     

Host specificity testing and suitability of a European biotype of the braconid parasitoid Microctonus aethiopoides as a biological control agent against Sitona lepidus (Coleoptera: Curculionidae) in New Zealand

The European biotype of the parasitoid Microctonus aethiopoides Loan (Hymenoptera: Braconidae) is being considered for release against Sitona lepidus Gyllenhal (Coleoptera: Curculionidae) in New Zealand. Host specificity was evaluated in the laboratory using both endemic and introduced weed biological control curculionid species, with 12 no-choice and three choice experiments carried out comparing the S. lepidus and test weevils. Two further no-choice tests used the Moroccan M. aethiopoides biotype to compare attack rate between European and Moroccan M. aethiopoides, the latter released in 1982 to control the lucerne pest S. discoideus. Across all experiments, total parasitism of S. lepidus was 69% compared with 15% for the test weevils. European M. aethiopoides was able to develop in the native weevils Irenimus aequalis, Nicaeana cervina, Catoptes cuspidatus, Protolobus porculus and Steriphus variabilis with parasitism rates of 13, 28, 2, 7 and 8%, respectively. These levels were significantly less than those in the corresponding S. lepidus control. Total parasitism of I. aequalis and C. cuspidatus increased significantly in the presence of S. lepidus than recorded under no-choice conditions. The presence of European M. aethiopoides caused minor, if any, test weevil mortality prior to the onset of prepupal emergence and there was no significant reproductive suppression in parasitoid-exposed test weevils. Parasitism of the introduced weed control agent R. conicus by European M. aethiopoides was significantly lower (1.1%) compared to the Moroccan biotype (47.5%). Based on these and other experiments, should the European M. aethiopoides be released as a biological control agent of S. lepidus, its ecological impacts are likely to be less severe than those already exhibited by the Moroccan M. aethiopoides.     

Strongylus asini (Nematoda, Strongyloidea): Genetic relationships with other strongylus species determined by ribosomal DNA

Genomic DNA was isolated from adult Strongylus asini collected from zebra. The second ribosomal transcribed spacer (ITS-2) was amplified and sequenced using polymerase chain reaction (PCR) based techniques. The DNA sequence was compared with previously published data for 3 related Strongylus species. A PCR-linked restriction fragment length polymorphism method allowed the 4 species to be differentiated unequivocally. The ITS-2 sequence of S. asini was found to be more similar to those of S. edentatus (87.1%) and S. equinus (95.3%) than to that of S. vulgaris (73.9%). This result confirms that S. asini and S. vulgaris represent separate species and supports the retention of the 4 species within 1 genus.     

Amplification and methylation of an esterase gene associated with insecticide-resistance in greenbugs, Schizaphis graminum (Rondani) (Homoptera: Aphididae)

The greenbug aphid, Schizaphis graminum (Rondani) has developed resistance to organophosphorus insecticides by the over-production of esterases that have been classified as Type I and Type II. The first twenty N-terminal amino acids of the Type I esterase were determined and used to design an oligonucleotide, which in conjunction with an active site primer derived from conserved sequences of other insect esterases and two internal primers specific for esterases from another aphid species resulted in a 0.85 kb genomic DNA fragment from resistant greenbugs. This was extended by 5′ RACE which provided approximately 1.2 kb of the 5′ end of the esterase gene. The 5′ DNA sequence corresponded to 19 of the 20 known amino acids of the Type I esterase, with the last needing only a one base change (probably resulting from a PCR artifact). Furthermore, the sequence showed very close similarity to the amplified E4/FE4 esterase genes of Myzus persicae (Sulzer). A comparison of sequences suggested that the S. graminum gene has introns in the same positions as the first two introns of E4/FE4, with the second intron being considerably larger in S. graminum. Probing of Southern blots with the 0.85 kb esterase fragment showed that the gene encoding the Type I esterase is amplified 4- to 8-fold in resistant S. graminum and that the amplified sequences contain 5-methylcytosine at MspI/HpaII sites, again in agreement with previous findings for M. persicae genes.     

Myriophyllum quitense Kunth (Haloragaceae) in Bolivia: A terrestrial growth-form with bisexual flowers

A terrestrial growth-form of Myriophyllum quitense growing in a lake bed in the interandean valley region of Bolivia represents the first report of a terrestrial growth-form for this species. While typically M. quitense possesses leaves and flowers in whorls of (3–) 4, this population is noteworthy for possessing 2–5% of individuals with both leaves and flowers in whorls of five, and for the presence of bisexual flowers. Observations regarding the distribution, habitat preferences and intraspecific variation of M. quitense in Bolivia are also given.     

防风根际真菌的分离鉴定及其生防潜力评价

作为世界性分布的镰刀属常见病原真菌,尖孢镰刀菌（Fusarium oxysporum）和木贼镰刀菌（F. equiseti）对包括经济作物及药用植物等的生长均有较大危害。利用源自于植物根际土壤的有益微生物防控尖孢镰刀菌和木贼镰刀菌引起的真菌性病害,是目前较为理想的植物病害管理策略。为获得可有效抑制尖孢镰刀菌和木贼镰刀菌的生防菌源,于防风根际土壤中分离纯化真菌104株,基于平板对峙法筛选获得1株对尖孢镰刀菌和木贼镰刀菌具有显著抑制效果的菌株MR-43,结合形态特征、ITS序列分析,将其确定为Sirastachys castanedae（GenBank登录号：OK287148.1）,隶属于Sirastachys组进化分支,发现其可宿生于植物根际土壤。基于盆栽试验法,探究MR-43在防风栽培土壤中的定殖能力,评价MR-43对由尖孢镰刀菌引起的防风枯萎病和由木贼镰刀菌引起的防风根腐病的防病能力,及其对防风植株的促生能力。结果显示,Sirastachys castanedae MR-43对尖孢镰刀菌、木贼镰刀菌的抑菌率为57%以上,且经多次验证抑菌效果稳定;菌株MR-43可稳定定殖于防风栽培土壤并实现有效扩繁;菌株MR-43的孢子悬液可有效控制防风枯萎病和防风根腐病,平均防效达68.52%,与多菌灵、代森锰锌的防病效果无显著性差异（P>0.05）;此外,MR-43对防风植株生长具有明显促进作用。因此,Sirastachys castanedae MR-43在防风枯萎病、根腐病等真菌性病害管理方面具有较好的开发价值及应用潜力。