Gametophyte morphogenesis of Mexican species of Pleopeltis (Polypodiaceae, subfamily Pleopeltoideae)

The development and morphology of the gametophytes of seven species of ferns from genus Pleopeltis are described and compared. The spore germination is Vittaria-type in P. astrolepis, P. crassinervata, P. macrocarpa, P. polylepis and P. revoluta. For P. angusta and P. mexicana it was proposed a new germination pattern is Pleopeltis-type. The prothallial development is Drynaria-type in P. astrolepis, P. crassinervata, P. macrocarpa, P. polylepis and P. revoluta and Ceratopteris-type for P. angusta and P. mexicana. The gametangia are typical of the leptosporangiate ferns, sporophytes after six and a half months in culture did not appeared.     

Phosphorus status of some saline and non-saline hydromorphic soils of the Niger Delta of Nigeria

Summary The phosphorus status of some mangrove and fresh-water hydromorphic soils of the Nigerian Niger Delta was evaluated by determining the relative abundance of various P forms and the P-sorption capacity indices. Total P was high in all soils ranging from 352 to 2055 mg/kg, with a mean of 1011 mg/kg. The saline mangrove-swamp soils had generally higher values than the fresh-water soils. Organic P formed about 34% of total P. The relative abundance of the inorganic P forms was in decreasing order, active P, occluded P and residual P. The relative distribution of active P followed the decreasing order, Fe–P, Al–P and Ca–P.The adsorption capacity was generally low in all soils. The amount of P sorbed from the addition of 150 mg/100g of soil ranged from zero to 13 mg/100g, giving an average of about 7% of added P sorbed.The abundance of active P and low content of occluded P were attributed to the poorly drained and unweathered nature of the soils. The low P adsorption suggests little capacity of the soils to fix P. The relatively high content of active P and the low P sorption capacity generally indicate high availability of P to plant in these soils.     

Role of proline residues in the expression and function of the human noradrenaline transporter

The aim was to investigate the roles of proline residues in extracellular loop 2 (P172, P183, P188 and P209) and transmembrane domains 2, 5, 11 and 12 (P108, P270, P526, P551, P552 and P570) in determining noradrenaline transporter (NET) expression and function. Mutants of human NET with these residues mutated to alanine were pharmacologically characterized. Mutation of P108, P270 and P526 disrupted cell surface expression, from [3H]nisoxetine binding and confocal microscopy data. Mutations of P526, P551 and P570 reduced transporter turnover (Vmax of [3H]noradrenaline uptake/Bmax of [3H]nisoxetine binding) by 1.5-1.7-fold compared with wild-type NET, so these residues might be involved in conformational changes associated with substrate translocation. Conversely, mutations of P172, P183, P188 and P209 increased Vmax/Bmax by 2-3-fold compared with wild-type, indicating that the presence of these proline residues limits turnover of the NET. The mutations had few effects on apparent affinities of substrates or affinities of inhibitors, except decreases in inhibitor affinities after mutations of the P270 and P570 residues, and increases after mutation of the P526 residue. Hence, proline residues in extracellular loop 2 and in transmembrane domains have a range of roles in determining expression and function of the NET.     

Turnover of the phosphomonoester groups of polyphosphoinositol lipids in unstimulated human platelets

The metabolic activity of the polyphosphoinositol lipids in unstimulated human platelets was studied by short-term labelling with [32P]Pi, by replacement of [32P]Pi from pre-labelled platelets with unlabelled phosphate, and by depriving the cells of metabolic ATP. Under short-term labelling conditions, the 4- and 5-phosphate groups of phosphatidylinositol 4-phosphate (PtdIns4P) and phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2] had the same specific 32P radioactivity as the gamma-phosphate of metabolic ATP. The specific 32P radioactivity of the 1-phosphates of phosphatidylinositol, PtdIns4P and PtdIns(4,5)P2 was similar, but only 4-13% compared to that of the ATP-gamma-phosphate. When [32P]Pi pre-labelled platelets were incubated with up to 25 mM of unlabelled phosphate, the displacement of the 32P label from PtdIns4P, PtdIns(4,5)P2 and metabolic ATP followed similar kinetics. Inhibition of ATP regeneration in platelets pre-labelled with [32P]Pi resulted in a rapid fall in metabolic ATP with a much slower fall in [32P]PtdIns(4,5)P2, whereas [32P]PtdIns4P increased initially. However, ATP turnover was not abolished, as indicated by the marked (25% of the control) incorporation of extracellular [32P]Pi into PtdIns4P and PtdIns(4,5)P2 in metabolically inhibited platelets. This low phosphate turnover may explain the relative resistance of PtdIns4P and PtdIns(4,5)P2 to metabolic inhibition. We conclude that PtdIns4P and PtdIns(4,5)P2 are present as a single metabolic pool in human platelets. Turnover of the 4- and 5-phosphates of PtdIns4P and PtdIns(4,5)P2 in unstimulated platelets is as rapid as that of the gamma-phosphate of metabolic ATP, and accounts for about 7% of basal ATP consumption.     

Recent data on the occurrence of species of the Paramecium aurelia complex in Europe

Among 15 species of the Paramecium aurelia complex known world-wide, 10 have been found in Europe, namely: P. primaurelia, P. biaurelia, P. triaurelia, P. tetraurelia, P. pentaurelia, P. sexaurelia, P. septaurelia, P. novaurelia, P. dodecaurelia, and P. tredecaurelia. Recent data on the frequency of occurrence of the species in Europe are given in the paper.     

国产兜兰属植物观赏价值评价及其在华南地区的应用前景分析

以植株的生长状况、整株姿态、叶片观赏性、开花性、花形、花色和花朵观赏期为评价指标,利用灰色关联分析,对我国原产的27种兜兰属植物的观赏价值进行了综合评价并分析了它们在华南地区的应用前景。结果表明:多花长瓣型的飘带兜兰与理想种的关联度最高,达到0.7304,是最值得在华南地区栽培的兜兰种类,其次为白旗兜兰。而紫纹兜兰、汉氏兜兰;文山兜兰、格利兜兰、带叶兜兰、亨利兜兰、同色兜兰,它们的关联度系数超过0.6;紫毛兜兰、巨瓣兜兰、红旗兜兰、天伦兜兰、长瓣兜兰、根茎兜兰的关联度均超过0.5;也是值得推广兜兰种类;杏黄兜兰、硬叶兜兰、白花兜兰由于生长状况差、开花性差等原因与理想种的关联度分别只有0.1900、0.1921、0.2917,不适于华南地区栽培;其它9种兜兰的关联度虽然介于0.35~0.50之间,但其中有些种类如虎斑兜兰、麻栗坡兜兰、波瓣兜兰、德氏兜兰等由于具有独特的观赏价值和育种潜力,也是值得在华南地区栽培的兜兰种类。     

Proteins of bacteriophage phi6.

We investigated the protein composition of the lipid-containing bacteriophage phi 6. We also studied the synthesis of phage-specific proteins in the host bacterium Pseudomonas phaseolicola HB10Y. The virion was found to contain 10 proteins of the following molecular weights: P1, 93,000; P2, 88,000; P3, 84,000; P4, 36,800; P5, 24,000; P6, 21,000; P7, 19,900; P8, 10,500; P9, 8,700; and P10, less than 6,000. Proteins P3, P9, and P10 were completely extracted from the virion with 1% Triton X-100. Protein P6 was partially extracted. Proteins P8 and P9 were purified by column chromatography. The amino acid composition of P9 was determined and was found to lack methionine. Labeling of viral proteins with [35S]methionine in infected cells indicated that proteins P5, P9, P10, and P11 lacked methionine. Treatment of host cells with UV light before infection allowed the synthesis of P1, P2, P4, and P7; however, the extent of viral protein synthesis fell off exponentially with increasing delay time between irradiation and infection. Treatment of host cells with rifampin during infection allowed preferential synthesis of viral proteins, but the extent of synthesis also fell off exponentially with increasing delay time between the addition of rifampin and the addition of radioactive amino acids. All of the virion proteins were seen in gels prepared from rifampin-treated infected cells. In addition, two proteins, P11 and P12, were observed; their molecular weights were 25,200 and 20,100, respectively. Proteins P1, P2, P4, and P7 were synthesized early, whereas the rest began to increase at 45 min post-infection.     

Plasmid-directed assembly of the lipid-containing membrane of bacteriophage phi 6.

The nucleocapsid of bacteriophage phi 6 is enveloped within a lipid-containing membrane. The membrane is composed of proteins P3, P6, P9, P10, and P13 and phospholipids. The relationship between membrane protein P9 and morphogenetic protein P12 was studied in the absence of phage infection. cDNA copies of genes 9 and 12 were expressed on plasmids in Pseudomonas syringae pv. phaseolicola. Immunoblotting demonstrated the presence of protein P9 in strains carrying both gene 9 and gene 12 but not in strains with gene 9 alone. In the absence of P12, P9 was found to be unstable. Simultaneous synthesis of proteins P9 and P12 led to the formation of a low-density P9 particle having a buoyant density similar to that of precursor structures composed of phospholipid and proteins isolated from phi 6-infected cells. These results are consistent with results of previous genetic experiments suggesting that P9 and P12 are necessary and sufficient for the formation of the phi 6 envelope. Extensions of P9 at the C terminus do not impair particle formation; however, N-terminal extensions or C-terminal deletions that extend into the hydrophobic region of P9 do impair particle formation.     

Opioid Receptors of Neuroblastoma Cells Are in Two Domains of the Plasma Membrane that Differ in Content of G Proteins

Opioid receptors of NG 108-15 cell membranes are distributed in two membrane fractions sedimenting at 20,000 g (P2) and 200,000 g(P3). The number of receptors is identical in P2 and P3, but in P2 all sites are present in one high-affinity state (2 nM), whereas in P3 60% of these receptors display lower affinity (150 nM). Upon addition of GTP or pretreatment with pertussis toxin, 80% of the sites exist in low affinity in both P2 and P3. Therefore, the effect of GTP and pertussis toxin on agonist binding appears to be smaller in P2 than in P3. In contrast, sodium inhibits agonist binding in P2 and P3 to the same extent and with identical potency. Opioid-mediated stimulation of GTPase is much greater in P2 than in P3, whereas inhibition of adenylate cyclase does not differ in the two fractions. Using site-specific antibodies and pertussis toxin-catalyzed ADP-ribosylation, we found that the amount of G proteins in P3 is only 30-50% of that in P2. Treatment of intact cells with the hydrophilic protein-modifying agent sulfosuccinimido-biotin results in biotinylation of proteins from both fractions and in a similar reduction of opioid binding in P2 and P3. Likewise, exposure of intact cells to the alkylating opioid antagonist, chlornaltrexamine, produces identical degrees of receptor inactivation in P2 and P3. The rate of in vivo pertussis toxin-mediated modification of G proteins is not different in the two fractions.(ABSTRACT TRUNCATED AT 250 WORDS)     

The effect of long-range loop-loop interactions on folding of the Tetrahymena self-splicing RNA

Bas?e-pairing between the terminal loops of helices P2.1 and P9.1a (P13) and P2 and P5c (P14) stabilize the folded structure of the Tetrahymena group I intron. Using native gel electrophoresis to analyze the folding kinetics of a natural pre-RNA containing the Tetrahymena intron, we show that P13 and P14 are the only native loop-loop interactions among six possible combinations. Other base-pairing interactions of the loop sequences stabilize misfolded and inactive pre-RNAs. Mismatches in P13 or P14 raised the midpoints and decreased the cooperativity of the Mg(2+)-dependent eqXuilibrium folding transitions. Although some mutations in P13 resulted in slightly higher folding rates, others led to slower folding compared to the wild-type, suggesting that P13 promotes formation of P3 and P7. In contrast, mismatches in P14 increased the rate of folding, suggesting that base-pairing between P5c and P2 stabilizes intermediates in which the catalytic core is misfolded. Although the peripheral helices stabilize the native structure of the catalytic core, our results show that formation of long-range interactions, and competition between correct and incorrect loop-loop base-pairs, decrease the rate at which the active pre-RNA structure is assembled.     

First European record of Paramecium septaurelia and the discovery of new European habitats of P. pentaurelia and P. sexaurelia in Russia (Astrakhan and Volgograd regions)

The presence of several species of the P. aurelia complex was revealed in the studied regions. In the Volgograd region P. primaurelia, P. biaurelia, P. triaurelia, and P. novaurelia were recorded. In the Astrakhan Nature Reserve P. primaurelia, P. pentaurelia, P. sexaurelia, and P. septaurelia were identified. Among these species, P. septaurelia was recorded for the first time in Europe, known before only from the territory of the USA, P. pentaurelia and P. sexaurelia are species rare in Europe. The studied regions are very rich in species of the P. aurelia complex and worthy of future studies.     

根际酸化作用对杨树无性系磷营养效率的影响

应用土培盆栽技术,研究了杨树P营养效率的无性系差异与根际酸化作用的关系。P处理设4个水平,分别为0、40、80和120mg·kg^-1(P2O5),每个处理重复3次。各用土40kg,随机排列．结果表明,在缺P胁迫下,P营养高效型无性系S17、S19和105的根际pH值明显降低,最大为1．32个单位。降幅均在10％以上;而P营养低效型无性系106、797、I-69、1388和3244的根际pH值的降低则很小。最大的仅为0．21个单位,降幅均在2．5％以下。高效型无性系的根际pH值。随缺P胁迫的增加而逐渐降低。一旦缺P胁迫缓和,根际pH值随之增高,低效型无性系则不具有这种反应机理。S17、S19和105在缺P胁迫环境下,根际有效磷分别为2．64、3．27和3．28mg·kg^-1,根际有效磷的积累率均在60％以上;而无性系106、797、I-69、1388和3244的根际有效磷均不足2．00mg·kg^-1,根际有效磷的积累率不足10％。高效型无性系在缺P胁迫环境下对P的吸收量显著高于低效型无性系,统计分析也证明,缺P胁迫条件下。无性系根际有效磷的积累与根际pH值降低呈显著相关。说明根际酸化作用是根际有效磷增加的原因。     

Attachment organelle formation represented by localization of cytadherence proteins and formation of the electron-dense core in wild-type and mutant strains of Mycoplasma pneumoniae

Cytadherence proteins of Mycoplasma pneumoniae are localized at the attachment organelle, which is involved in adhesion, gliding motility, and cell division. The localization of these proteins in cytadherence-deficient mutants was examined by immunofluorescence microscopy. In the class I-2 mutant, which has a frameshift mutation in the hmw2 gene, fluorescent foci for HMW1 and HMW3 were found with reduced intensity, and P1 adhesin showed reduced focusing. However, foci for P90, P40, P30, and P65 were not observed in this mutant. In the class IV-22 mutant, which lacks expression of P1, P90, and P40, the other cytadherence proteins (HMW1, HMW3, P30, and P65) were focused. In a mutant lacking HMW1, signals for HMW3, P90, P40, P30, and P65 were not found, and P1 was distributed throughout the cell. These results suggest that HMW1 is essential for the localization of all other cytadherence proteins, while HMW2 is essential for the localization of P90, P40, P30, and P65. The electron-dense core in cytadherence mutants was observed by thin-section electron microscopy, suggesting that its formation depends on HMW1 and HMW2 and that P1 localization occurs independent of the formation of the electron-dense core. Doubly stained preparations visualized by immunofluorescence microscopy showed that the P1 adhesin, P90, and P40 colocalized to a subregion of the attachment organelle in the wild-type strain. HMW1 and HMW3 also colocalized to a different subregion of the attachment organelle, while P30 and P65 localized at more distal ends of cell poles than HMW1 and HMW3. These differences were more pronounced in cytadherence mutants. These results suggest that there are three distinct subcellular protein localization sites in the attachment organelle, which were represented by HMW1-HMW3, P1-P90-P40, and P30-P65.     

Role of alpha-helical conformation of histatin-5 in candidacidal activity examined by proline variants

Human salivary histatin-5 (Hsn-5) is a potent in vitro anticandidal agent. The aim of this study was to investigate the importance of alpha-helical structure of Hsn-5 for its candidacidal activity. The following three Hsn-5 variants, where one or more functionally nonessential residues were replaced with proline (potent alpha-helix breaker), were produced by Escherichia coli expression system: H21P (1P), H19P/H21P (2P), and E16P/H19P/H21P (3P). The activities of purified proteins were determined by candidacidal assays, and the secondary structures by circular dichroism (CD) spectroscopy in trifluoroethanol (TFE) that is considered the helix-promoting solvent, and lysophosphatidyl-glycerol (LPG) micelles, the environment that more closely resembles the biological membranes. Our results indicated that 3P variant displayed a candidacidal activity which was similar to that of unaltered Hsn-5 (0P), while 1P and 2P variants showed lower cidal activity. The CD spectra in TFE indicated that 3P variant has less helical characteristics than the 0P, 1P and 2P. These results suggested that the alpha-helical content of Hsn-5 proline variants does not correlate with the candidacidal activity. Further, the CD spectral analysis of peptides in LPG micelles indicated the formation of beta-turn structures in 0P and 3P variants. In conclusion, 3P variant which exhibited comparable candidacidal activity to 0P contains lower percentage of alpha-helical structure than 1P and 2P variants, which exhibited lower candidacidal activity. This suggests alpha-helix may not be important for anticandidal activity of Hsn-5.     

A cytotaxonomic study of some species of Pleione D. Don (Orchidaceae)

For taxonomic purposes in the genus Pleione D. Don (Orchidaceae) breeding studies, chromosome numbers, karyotypes and analyses of pollen mother cells have been investigated. In addition to confirming many previous chromosome numbers, new tetraploid, hexaploid and triploid counts establish the existence of a tetraploid taxon (P. speciosa) , a hexaploid (P. bulbocodioides) and a triploid hybrid (P.humilis 'Frank Kingdon-Ward'). The karyotypes of the diploid species P. bulbocodioides, P.yunnanensis, P. humilis, P.forrestii and P. hookeriana are distinct, whereas those of P.formosana and P. limprichtii have similar morphology to that of P. bulbocodioides , which was also represented in the polyploid taxa. Karyotype morphology provides evidence to trace the putative parents of P. x confusa and P. humilis 'Frank Kingdon-Ward'. Results from pollen mother cells and karyotype analyses suggest that P.formosana and P. limprichtii are not cytologically differentiated from P. bulbocodiodes , and the taxa P. speciosa, P. limprichtii (tetraploid form) and P. bulbocodioides (6x) are of autopolyploid origin, being derived from the P. bulbocodioides genome. The species limits are discussed.     

Mechanism for the regulation of mammalian cGMP phosphodiesterase6. 2: Isolation and characterization of the transducin-activated form

Rod photoreceptor cGMP phosphodiesterase (PDE6) consists of a catalytic subunit complex (Pαβ) and two inhibitory subunits (Pγ). In the accompanying article, using bovine photoreceptor outer segment homogenates, we show that Pγ as a complex with the GTP-bound transducin α subunit (GTP-Tα) dissociates from Pαβγγ on membranes, and the Pαβγγ becomes Pγ-depleted. Here, we identify and characterize the Pγ-depleted PDE. After incubation with or without guanosine 5′-O-(3-thiotriphosphate) (GTPγS), Pαβ complexes are extracted. When a hypotonic buffer is used, Pαβγγ, Pαβγ, and a negligible amount of a Pαβ complex containing Pγ are isolated with GTPγS, and only Pαβγγ is obtained without GTPγS. When an isotonic buffer containing Pδ, a prenyl-binding protein, is used, Pαβγγδ, Pαβγδδ, and a negligible amount of a Pαβ complex containing Pγ and Pδ are isolated with GTPγS, and Pαβγγδ is obtained without GTPγS. Neither Pαβ nor Pαβγγ complexed with GTPγS-Tα is found under any condition we examined. Pαβγ has ~12 times higher PDE activity and ~30 times higher Pγ sensitivity than those of Pαβγγ. These results indicate that the Pγ-depleted PDE is Pαβγ. Isolation of Pαβγγδ and Pαβγδδ suggests that one C-terminus of Pαβ is involved in the Pαβγγ interaction with membranes, and that Pγ dissociation opens another C-terminus for Pδ binding, which may lead to the expression of high PDE activity. Cone PDE behaves similarly to rod PDE in the anion exchange column chromatography. We conclude that the mechanisms for PDE activation are similar in mammalian and amphibian photoreceptors as well as in rods and cones.     

Purification of two isozymes of rat liver microsomal cytochrome P450 with testosterone 7 alpha-hydroxylase activity

Cytochrome P450a was purified to electrophoretic homogeneity from liver microsomes from immature male Long-Evans rats treated with Aroclor 1254. Rabbit polyclonal antibody raised against cytochrome P450a cross-reacted with cytochromes P450b, P450e, and P450f (which are structurally related to cytochrome P450a). The cross-reacting antibodies were removed by passing anti-P450a over an N-octylamino-Sepharose column containing these heterologous antigens. The immunoabsorbed antibody recognized only a single protein (i.e., cytochrome P450a) in liver microsomes from immature male rats treated with Aroclor 1254 (i.e., the microsomes from which cytochrome P450a was purified). However, the immunoabsorbed antibody recognized three proteins in liver microsomes from mature male rats, as determined by Western immunoblot. As expected, one of these proteins (Mr 48,000) corresponded to cytochrome P450a. The other two proteins did not correspond to cytochromes P450b, P450e, or P450f (as might be expected if the antibody were incompletely immunoabsorbed), nor did they correspond to cytochromes P450c, P450d, P450g, P450h, P450i, P450j, P450k, or P450p. One of these proteins was designated cytochrome P450m (Mr approximately 49,000), the other cytochrome P450n (Mr approximately 50,000). Like cytochrome P450a, cytochrome P450n was present in liver microsomes from both male and female rats. However, whereas cytochrome P450a was detectable in liver microsomes from 1-week-old rats, cytochrome P450n was barely detectable until the rats were at least 3 weeks old. Furthermore, in contrast to cytochrome P450a, the levels of cytochrome P450n did not decline appreciably with age in postpubertal male rats. Cytochrome P450m was detectable only in liver microsomes from postpubertal (greater than 4 week-old) male rats. Cytochromes P450m and P450n were isolated from liver microsomes from mature male rats and purified to remove cytochrome P450a. When reconstituted with NADPH-cytochrome P450 reductase and lipid, cytochrome P450n exhibited little testosterone hydroxylase activity, whereas cytochrome P450m catalyzed the 15 alpha-, 18-, 6 beta-, and 7 alpha-hydroxylations of testosterone at 10.8, 4.6, 2.0, and 1.9 nmol/nmol P450/min, respectively. The ability of cytochrome P450m to catalyze the 7 alpha-hydroxylation of testosterone was not due to contamination with cytochrome P450a, which catalyzed this reaction at approximately 25 nmol/nmol P450a/min. Cytochrome P450m also converted testosterone to several minor metabolites, including androstenedione and 15 beta-, 14 alpha-, and 16 alpha-hydroxytestosterone.(ABSTRACT TRUNCATED AT 400 WORDS)     

高产磷高效水稻磷素吸收利用特征

通过正常供磷的大田试验（2011年）,以产量和磷籽粒生产效率为指标,将27份中熟水稻亲本材料划分为4个类型,再通过正常和低磷处理的土培试验（2012年）,筛选出高产磷高效水稻材料,并探讨各种磷效率对产量的贡献率.结果表明： 结合两年的试验结果,供试材料的产量和磷利用效率均存在显著的基因型差异,筛选出GR泸17/矮TTP//泸17_2（QR20）为高产磷高效材料.在两个供磷水平下,QR20的产量和磷利用效率均显著高于低产磷低效材料玉香B,其产量分别是玉香B的1.96和1.92倍.大田和土培试验结果均表明,磷积累量对产量的贡献率均高于磷籽粒生产效率和磷收获指数.正常供磷条件下,磷积累量和磷籽粒生产效率对产量的贡献率差异不大,低磷条件下差异较大（66.5%和26.6%）,磷收获指数对产量的贡献率最低,最高仅为11.8%（土培）.土培试验中,正常供磷条件下,拔节-抽穗阶段的磷积累量对产量和磷收获指数的贡献率最高,分别为93.4%和85.7%,对磷籽粒生产效率的贡献率为41.8%;在低磷条件下,分蘖-拔节阶段的磷积累量对产量和磷籽粒生产效率的贡献率最高,分别为56.9%和20.1%,对磷收获指数的贡献率为16.0%.土培正常供磷条件下,水稻QR20的产量、磷积累量和磷收获指数相对于低磷处理分别增加了20.6%、18.1%和18.2%,差异显著.综上,磷效率对水稻产量的贡献率大小依次为磷吸收效率＞利用效率＞转运效率;正常供磷条件下,拔节-抽穗阶段的磷积累量对产量的贡献率最高,低磷胁迫下,分蘖-拔节阶段的磷积累量对产量的贡献率最高,这两个阶段可能是水稻高产磷高效协调统一的关键时期.
     

猪圆环病毒PCR检测方法的优化

猪圆环病毒(Porcine circovirus,PCV)为无囊膜的单股负链DNA病毒,是目前发现的最小的动物病毒,大小约为17nm[1]。PCV根据抗原性及基因组的不同可以分为PCV1和PCV2两种基因型,PCV1分离自猪肾细胞系PK15,它不致病,能够在PK15中稳定存在而不形成细胞病变;PCV2对猪有致病性,可引起猪断奶后多系统衰竭综合征(PMWS)、猪皮炎与肾病综合征(PDNS)、断奶猪和育肥猪的呼吸道疾病、猪的繁殖障碍等疾病。近年来已成为严重危害我国养猪业的主要疾病之一。但迄今为止市场上还没有商品化疫苗和特效药物防治该病,并且该病有时呈亚临床感染,所以…