Haemophilus influenzae antibiotic resistant strains isolated in Moscow in 2002-2004]

The results of 3-year observation on emergence of H. influenzae antibiotic resistant strains in Moscow are summarized. The study included 566 strains isolated from patients in 2002-2004. The susceptibility was determined by the 2-fold microdilution method on the Haemophilus test medium. The percentage of the resistant strains isolated in 2002, 2003 and 2004 was the following: ampicillin --4.9, 3.2 and 3.6%, tetracycline--3.3, 3.2 and 1.8% and co-trimoxazole--10.9, 20.9 and 20% respectively. The strains isolated in 2003 and 2004 were resistant to azithromycin in 0.6 and 1.8% of the isolates and to clarithromycin in 1.3 and 3.2% of the isolates respectively. Five isolates differed by the minimum resistance to ampicillin whereas producing no beta-lactamase (BLNAR strains). The drugs of choice for the treatment of respiratory tract infections mainly due to H. influenzae, i.e. acute otitis and sinusitis, chronic bronchitis exacerbation and sometimes pneumonia remain betalactam antibiotics. From the microbiological viewpoint the inhibitor-protected aminopenicillins, cefuroxime and cefotaxime have no significant advantages vs. amoxycillin. The use of cotrimoxazole and chloramphenicol should be considered inexpedient.     

The use of clip cages to restrain insects reduces leaf expansion systemically in Rumex obtusifolius

Abstract. 1. Clip cages have been used widely by experimental ecologists to contain insects on plants.
2. Under controlled conditions, the effect of applying clip cages alone and clip cages and the chrysomelid beetle Gastrophysa viridula on systemic leaf expansion of Rumex obtusifolius was investigated. Treatments were applied to the fully expanded fourth leaf and expansion of leaf 8 was measured over a period of 22 days.
3. The application of clip cages reduced the rate at which leaf area increased and led to reductions in final leaf areas.
4. Clip cages have systemic effects on plant development and these effects are sustained even after the clip cage is removed. Investigators should take this into account in designing experiments.     

GENESIS OF THE APYRENE PARASPERM IN THE APPLE SNAIL POMACEA CANALICULATA (GASTROPODA: AMPULLARIIDAE): AN ULTRASTRUCTURAL STUDY

The apyrene paraspermatogenesis in the freshwater gastropod Pomaceacanaliculata has been studied with electron microscopy. Matureapyrene parasperm result from a cytodifferentiation processwithout maturation division. The atypical condition is recognizedearly. Paraspermatogonia are characterized by voluminous nucleiwith irregular clusters of heterochromatin, numerous dilated cisternaeof the rough endoplasmic reticulum and small electron-dense granulesspread through the cytoplasm. As this process advances, the nucleibecome lobed and chromatin degenerates. The remnant chromatin condensesto form dense bodies which are finally excreted from the cells.At the cytoplasmic level a centriolar multiplication with the consequentflagellogenesis takes place. The axonemal microtubules run alongthe entire length of the cell and emerge from the posteriorend forming a tuft of three or more free flagella. The roughendoplasmic reticulum and the Golgi complex are involved inthe production of secretory granules, some of which are laterreleased by exocytosis. At the end of paraspermatogenesis matureapyrene parasperm are fusiform-shaped anuclear ciliated cells. (Received 20 January 2000; accepted 18 July 2000)     

Expansion of repetitive DNA into cytogenetically visible elements.

Two cases of amplified repetitive elements accidentally identified in cancer samples are reported. In both cases, repeated DNA that is normally not visible by traditional chromosome banding had increased in amount to become cytogenetically visible. In one case, an addition to the short arm of chromosome 1 was originally diagnosed. However, upon molecular analysis the diagnosis could be corrected to an amplification of the D1Z2 repeat. In the second case, a strongly DAPI-positive band was visible at the top of the short arm of chromosome 22, and the original diagnosis was add(22). Staining for telomeric repeats revealed their presence inside the DAPI-positive element, thus confirming that the element in question was truly added to the end of the chromosome. Curiously, no telomeric repeats could be detected distal to the DAPI-positive element. The identity of the DAPI-positive element could not be established, as it was not stained by any of the specific probes applied, nor in a scanning hybridization with labeled Cot-1 DNA. It thus seems to represent an expansion from some lowly repetitive AT-rich DNA translocated to the tip of chromosome 22.     

Monosynaptic pathway responsible for generation of bursting activity in theHelix pomatia RPal neuron

The connection between a visceral ganglia interneuron initiating bursting pacemaker activity in the RPal neuron and the RPal neuron itself was investigated inHelix pomatia. Stimulating the interneuron either initiated or intensified bursting activity in the RPal neuron, depending on initial electrical activity in this cell. Replacing calcium with magnesium ions in the extracellular fluid and adding CdCl₂ to this fluid reversibly inhibited the effect of interneuronal stimulation on the RPal neuron. The latter effect was unaffected by increasing the concentration of extracellular Ca²⁺ 10 to 70 mM. Intracellular injection of both Cs⁺ and TEA into the interneuron produced an increase in the duration of its action potentials and rendered the link connecting the neurons more effective. It is deduced that a monosynaptic chemical connection exists between the interneuron and the RPal neuron for which a peptide compound serves as transmitter.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 19, No. 1, pp. 20–28, January–February, 1987.     

Short-term movements of chalk-stream invertebrates

SUMMARY 1. Trays of gravel were implanted for 24 h periods in several chalk streams. The trays were variously modified to monitor colonization from different sources, particularly drift (D), other downstream movements (DSM), upstream movements (USM), and all sources combined (ALL).
2. The abundance of invertebrates in the streams was high (maximum of 717 per 0.04 m²) and colonization of the trays was extensive, especially by Gammarus pulex , the predominant species in all but one of the streams (maximum number of individuals of G. pulex per tray: for D, 473; for DSM, 462; tor USM, 286; and tor ALL, 639). In some cases benthic densities were achieved in the trays in the 24 h exposure period, and in most cases any one source of colonization could provide benthic densities in a few days.
3. Patterns of movement differed between species, between size classes of G. pulex , and between sites for particular species. No one source of colonization could be regarded as generally predominant although downstream movements in total (D + DSM) usually far exceeded USM. DSM was usually an important source of colonization.
4. The extent and direction of movement appeared to be determined by local factors and were explained in terms of the high densities of invertebrates and the current and substratum characteristics of each site.
5. Estimates of the relative importance of different sources of colonization varied greatly according to the criteria used in determining proportions.     

Construction of DNA-probes and their immunochemical detection using nonradioactive hybridization tests

Simple and efficient chemical approaches to preparation of DNA probes carrying 2,4-dinitrophenyl, dansyl or biotin residues were developed. The residues were introduced using following DNA derivatization procedures: a) transamination of cytidine residues with O-(4-aminobutyl)hydroxylamine; b) mercuration of pyrimidine residues followed by beta-mercaptoethanol modification. It was shown that 2,4-dinitrophenyl-containing DNA probes can be used for nonradioactive hybridization detection of nucleic acids. DNP-DNA: DNA complexes were detected using mouse antibodies specific to 2,4-dinitrophenyl groups, which were developed with peroxidase-conjugated antimouse immunoglobulins. Peroxidase-catalyzed chemoluminescent reaction of luminol oxidation with hydrogen peroxide allowed to detect 10 picograms of the dinitrophenylated single-stranded DNA probe.