中国鲤科鱼类染色体组型的研究Ⅸ.鳊亚科9种鱼和鲴亚科1种鱼的染色体组型

我们曾报道过分布于湖北省的鳊、鲴亚科鱼类的核型。本文继续报道采自四川和广东省的鳊、鲴亚科另10种鱼的核型考察结果。       

楚科奇海及其海台区粒度分级叶绿素a与初级生产力

2003年夏季中国第二次北极科学考察期间,在楚科奇海及其海台区进行了叶绿素a浓度与初级生产力的现场观测。结果表明,观测海区叶绿素a浓度范围为0.009～30.390μg/dm3。表层浓度为0.050～4.644μg/dm3,平均值为(0.875±0.981)μg/dm3;陆架区次表层和底层的浓度高于表层,海台区深层水的浓度较低,200m层的浓度为(0.015±0.007)μg/dm3。水柱平均叶绿素a浓度区域性特征明显,陆架区高于海台区。R断面进行3趟重复观测,平均叶绿素a浓度分别为(2.564±1.496)μg/dm3,(1.329±0.882)μg/dm3和(0.965±0.623)μg/dm3,浓度呈下降趋势。观测站潜在初级生产力为0.263～4.186mgC/(m.3h),陆架区平均潜在初级生产力((2.305±1.493)mgC/(m.3h))比海台区((0.527±0.374)mgC/(m.3h))高近4倍。平均同化数为(1.22±1.14)mgC/(mgChla.h)。观测区细胞粒径>20μm的小型浮游生物对总叶绿素a浓度和初级生产力的贡献率分别为63.13%和65.16%,细胞粒径2.0～20μm的微型浮游生物和细胞粒径<2.0μm的微微型浮游生物对总叶绿素a和初级生产力的贡献率相差甚小,其对总叶绿素a浓度的贡献率分别为19.18%和17.69%,对总初级生产力的贡献率分别为20.11%和14.73%。     

鱼类远缘杂交正反交杂种胚胎发育差异的细胞遗传学分析

本文报道了鲤(Cyprinus carpio)×鲢(Hypophthalmichthys molitrix)、鲫(Carassiusauratus)×鲢、白鲫(Carassius auratus cuvieri)×鲢和鲢×鲤、鲢×鲫、鲢×白鲫的正反交试验。在鲤×鲢、鲫×鲢和白鲫×鲢3个正交组中,胚胎发育基本正常,尽管孵出的鱼苗绝大多数生命力弱,但孵化率都在50％左右;而在鲢×鲤、鲢×鲫和鲢×白鲫3个反交组中,胚胎发育均为畸形,不能孵化出苗。 胚胎发育细胞遗传学分析表明,鲤×鲢、鲫×鲢和白鲫×鲢的杂种胚胎几乎都是整倍体,而鲢×鲤、鲢×鲫×鲢×白鲫的杂种胚胎基本上是非整倍体,染色体数变化较大。这些正反交杂种胚胎发育的显著差异可能与其亲本物种间的基因组大小有关。文中还分析讨论了这些正反交差异与天然多倍体物种以及胚胎发育速度的相关性,认为天然多倍体物种可能具有一些不同于普通二倍体物种协调外源基因组的能力。     

SARS病毒巨细胞病毒合并感染真菌及其染色方法的应用比较

目的几种染色方法显示星形隐球菌和曲菌的比较。方法Grocott-Gomori六胺银改良法,Gomori氏嗜银法和PAS结果Grocott-Gomori氏六胺银改良法显示上述两种真菌效果最好,该法对真菌的显示颜色鲜艳,图像清晰,真菌的孢子和菌丝被染成深黑色,易与其它成份相区别;Gomori氏嗜银法对大量含有菌丝的组织有一定的染色效果,PAS法也能将上述两种真菌显示出来,但所着染成份较多,较难区别。结论Grocott-Gomori氏六胺银改良法是染真菌的最好方法。     

A new Multi-PCR-SSCP assay for simultaneous detection of isoniazid and rifampin resistance in Mycobacterium tuberculosis

Prompt detection of drug resistance in Mycobacterium tuberculosis is essential for effective control of tuberculosis (TB). We developed a Multi-PCR-SSCP method that detects more than 80% commonly observed isoniazid (INH) and rifampin (RIF) resistance M. tuberculosis in a single assay. The usefulness of the newly developed method was evaluated with 116 clinical isolates of M. tuberculosis. Distinct SSCP patterns were observed for different mutations and the correlation between Multi-PCR-SSCP results and DNA sequencing data was strong. Using the culture-based phenotypic drug susceptibility testing as a reference, the sensitivity of the newly developed Multi-PCR-SSCP assay was determined to be 80% and 81.8% for INH and RIF, respectively. The specificity of the assay was 100% and 92%, for INH and RIF, respectively. Multi-PCR-SSCP provides a rapid and potentially more cost-effective method of detecting multidrug-resistant TB.     

Size-fractionated chlorophyll a and primary productivity in the Chukchi Sea and its northern Chukchi Plateau

Investigations on chlorophyll a and primary productivity were carried out in the Chukchi Sea and its northern Chukchi Plateau during the 2^nd Chinese National Arctic Research Expedition in the summer of 2003. The results showed that chlorophyll a concentrations were 0.009–30.390 μg/dm³ at the surveyed waters; the surface chlorophyll a concentrations were 0.050–4.644 μg/dm³ and the average value was (0.875±0.981) μg/dm³ in the surveyed area. In the Chukchi Sea Shelf, chlorophyll a concentrations at the depth from 10 m to bottom were higher than that in the surface water, and the concentrations were lower at the depth below 75 m in the Chukchi Plateau. Chlorophyll a concentrations descended in 3 sequential samplings on Transect R, with average values of (2.564±1.496) μg/dm³, (1.329±0.882) μg/dm³ and (0.965±0.623) μg/dm³, respectively. The potential primary productivity ((2.305± 1.493) mgC/(m³·h)) in the Chukchi Sea was higher than that ((0.527±0.374) mgC/(m³·h)) in the Chukchi Plateau. The results of the size-fractionated chlorophyll a and primary productivity showed that microplankton accounted for the majority of the total chlorophyll a (63.13%) and primary productivity (65.16%) at the survey stations. The contributions of the nanoplankton and picoplankton to the total chlorophyll a and primary productivity were roughly the same.     

Genomic polymorphism of the pandemic A (H1N1) influenza viruses correlates with viral replication, virulence, and pathogenicity in vitro and in vivo

The novel pandemic A (H1N1) virus was first identified in Mexico in April 2009 and quickly spread worldwide. Like all influenzas, the H1N1 strain-specific properties of replication, virulence, and pathogenicity are a result of the particular genomic sequence and concerted expression of multiple genes. Thus, specific mutations may support increased virulence and may be useful as biomarkers of potential threat to human health. We performed comparative genomic analysis of ten strains of the 2009 pandemic A (H1N1) influenza viruses to determine whether genotypes associated with clinical phenotypes, which ranged from mild to severe illness and up to lethal. Virus replication capacity was tested for each strain in vitro using cultured epithelial cells, while virulence and pathogenicity were investigated in vivo using the BALB/c mouse model. The results indicated that A/Sichuan/1/2009 strain had significantly higher replication ability and virulence than the other strains, and five unique non-synonymous mutations were identified in important gene-encoding sequences. These mutations led to amino acid substitutions in HA (L32I), PA (A343T), PB1 (K353R and T566A), and PB2 (T471M), and may be critical molecular determinants for replication, virulence, and pathogenicity. Our results suggested that the replication capacity in vitro and virulence in vivo of the 2009 pandemic A (H1N1) viruses were not associated with the clinical phenotypes. This study offers new insights into the transmission and evolution of the 2009 pandemic A (H1N1) virus.     

Enhanced anti-angiogenic effect of a deletion mutant of plasminogen kringle 5 on neovascularization

Kringle 5 (K5), a proteolytic fragment of plasminogen, has been proved to be an angiogenic inhibitor. Previously, we have evaluated the effect of K5 on the vascular leakage and neovascularization in a rat model of oxygen-induced retinopathy. In this study, we expressed K5 and a deletion mutant of K5 (K5 mutant) in a prokaryocyte expression system and purified them by affinity chromatography. K5 mutant was generated by deleting 11 amino acids from K5 while retaining the three disulfide bonds. The anti-angiogenic activity of intact K5 and K5 mutant were compared in endothelial cells and retinal neovascularization rat model. K5 mutant inhibited the proliferation of primary human retinal capillary endothelial cells (HRCEC) in a concentration-dependent manner, with an apparent EC50 of approximate 35 nmol/L, which is twofold more potent than intact K5. In the even higher concentration range, K5 mutant did not inhibit pericytes from the same origin of HRCEC, which suggested an endothelial cell-specific inhibition. K5 mutant had no effect on normal liver cells and Bel7402 hepatoma cells even at high concentration range either. Intravitreal injection of the K5 and mutant in the oxygen-induced retinopathy rat model both resulted in significantly fewer neovascular tufts and nonperfusion area than controls with PBS injection, as shown by fluorescein angiography. Furthermore, K5 mutant exhibited more strong inhibition effect on neovascularization than intact K5 by quantification of vascular cells. These results suggest that this K5 deletion mutant is a more potent angiogenic inhibitor than intact K5 and may have therapeutic potential in the treatment of those disorders with neovascularization, such as solid tumor, diabetic retinopathy, age-related macular degeneration, rheumatoid arthritis, and hyperplasia of prostate.     

Target syntheses of saturated Keggin polyoxometalate-based extended solids

By the approach of target synthesis, three infinitely extended hybrid compounds based on the saturated Keggin polyoxoanions have been synthesized under hydrothermal conditions: , and (phen = 1,10-phenanthroline, trea = triethylamine). The isostructural compounds 1 and 2 belong to the monoclinic space group P2₁/c and both contain neutral 2D layers and discrete polyoxometalate clusters decorated by transitional metal complexes. They represent an important example of the family of intercalated solids, in which both the 2D layers and the intercalated molecules are polyoxometalates with covalently linked transitional metal complex fragments. Compound 3, crystallizing in the monoclinic space group C2/c, consists of 1D zigzag chains constructed from alternating polyoxoanions and [Ni(phen)₂]²⁺ fragments. More interestingly, these three compounds are constructed directly from saturated polyoxometalates, in which the intact skeletons of Keggin clusters are maintained under hydrothermal conditions. Variable-temperature magnetic susceptibility measurements of compounds 1 and 2 reveal the feature of antiferromagnetic exchange interaction in these compounds.