Tetracycline-resistant Chlamydia trachomatis in Toulouse, France.

We report the first isolation of a tetracycline-resistant Chlamydia trachomatis strain in Toulouse, France. Culture of a post treatment endocervical specimen from a woman treated with tetracycline grew C. trachomatis. The patient was retreated with pristinamycin and cured. The minimal inhibitory concentration (MIC) and the minimal bactericidal concentration (MBC) of tetracycline for the patient isolate were > 64 micrograms/ml although 1% of the population of organisms showed resistance. Conversely for 34 C. trachomatis isolates recovered since 1988 from patients before treatment, in Toulouse, all the MICs of tetracycline were < or = 0.25 microgram/ml. If the isolation of tetracycline-resistant C. trachomatis was the result of persisting organisms, the management of chlamydial infections could be changed.

Characteristics of saliva secreted by patients with TCM-Piyinxu.

AIM: To investigate various characteristics of saliva secreted by patients with TCM-Piyinxu (Spleen-yin deficiency). METHODS: Twenty-five individuals with Piyinxu (15 males and 10 females; age range 26-70 years, mean age = 45 years) diagnosed based on criteria used in traditional Chinese medicine, were compared with 20 individuals with Shenyinxu (Kidney-yin deficiency) (11 males, 9 females; age range 35-75 years, mean age = 50) and 30 normal individuals (17 males, 13 females; age range 35-65 years, mean age = 49 years). After acid stimulation, the saliva flow in each group was measured, and the levels of amylase and protein in saliva were determined using an automatic biochemical analyzer. The resultant data were analyzed using the Kruskal-Wallis test and one-way factorial ANOVA test. RESULTS: The flow rates of saliva and amylase in Piyinxu patients (0.27 ± 0.016 mL/min and 2134.13 ± 343.51 IU/min, respectively) were lower than those in normal subjects (0.46 ± 0.027 mL/min and 3501.63 ± 1099.63 IU/min, respectively, P < 0.01), but higher than those in the Shenyinxu group (0.13 ± 0.051 mL/min and 951.62 ± 383.17 IU/min, respectively, P < 0.01). The three groups showed no significant difference in their level of total salivary protein (Piyinxu group, 3.07 ± 0.60 g/L; Shenyinxu group, 3.01 ± 0.90 g/L, and control group, 2.94 ± 1.13 g/L, P = 0.869), amount of amylase per saliva volume, or their ratio of amylase to protein in secreted saliva (P = 0.173 and P = 0.436, respectively). CONCLUSION: Piyinxu patients showed altered rates of saliva and amylase secretion when compared with those parameters in patients with Shenyinxu and normal subjects.

Electron microscopy of DNA molecules from blastoderm nuclei and yolk granules beneath blastoderm of fertilized and unincubated chicken eggs.

The DNA molecules isolated from the blastoderm nuclei and yolk granules beneath the blastoderm of fertilized and unincubated chicken eggs were observed under electron microscope, using the DNA sample of calf thymus as control. The results showed that both nuclear and yolk DNAs are linear, and their molecules are very similar to those of thymus DNA in shape. Since chromatin was first prepared from blastoderm nuclei and yolk granules respectively and then DNA was isolated from both of chromatin samples, it could be concluded that yolk granules possess both DNA chromatin as nuclei do.

Chromatin and DNA of yolk granules beneath "blastoderm region" of unfertilized chicken egg.

Electron microscopic study shows that the chromatin structure of yolk granules beneath the "blastoderm region" of the unfertilized chicken egg is identical to that of yolk granules beneath the blastoderm of the fertilized and unincubated chicken egg, and both chromatin structures are very similar to those of blastoderm nuclei. Furthermore the molecular shapes of DNA of both yolk granules are also very similar to those of the blastoderm nuclei, being all linear. Based on these observations, we have come to the conclusion that chromatin and DNA widely exist in the yolk when yolk granules have reached their development-specified competence. The results indicate further that the yolk granules are capable of synthesizing DNA, and provide the condition for the interaction of DNA with histones to form chromatin through self-organization.

Electron microscopic studies on the chromatin of blastoderm nuclei and yolk granules beneath blastoderm of fertilized and unincubated chicken eggs.

Chromatin prepared both from the yolk granules beneath the blastoderm and from the nuclei of the blastoderm cells of fertilized and unincubated chicken eggs was examined under electron microscope and its structure was compared. The results indicate that the above two kinds of chromatin fibers seem to have no apparent difference in structural relation and diameter. The electron microscopic appearances of the basic structures of both kinds of chromatin are all "beads-on-a-string"-shaped filaments. After the digestion of chromatin from both raw materials with DNase I, the connecting strings of chromatin fibers were cut off, only the scattered beads could be observed under electron microscope. The diameter of the scattered beads is equal to that of the beads on the chromatin fibers, and most of them are 150 A in diameter.

Time-lapse microcinematographic and phase contrast studies on the cell reformation of Chirocephalus yolk granules in vitro.

In this article we report on a time-lapse microcinematographic and phase contrast study of the cell reformation of yolk granules which were isolated from mature oocytes in the genital sac of the middle female intersex of Chirocephalus nankinensis. The observations on yolk granules were made in fixed positions and the morphological changes of cell reformation were continuously recorded in vitro. The transformation of yolk granules into cellular structures may be tentatively described as follows: At the early stages in culture, it can be seen that the granular or bubbly structures gradually appear within the hyaloid and homogeneous yolk granules; the appearance of yolk granules gradually changes from elliptical into round shape. With further transformation, their appearances in general take the shape of oblate spheroids, their size is smaller than before and inside the yolk granules their granular and bubbly structures become more and more obvious. Finally, the nuclear and cellular structures can be seen in these transforming yolks. By means of time-lapse microcinematographic and phase contrast examinations in fixed positions, single yolk granules obtained from the mature oocyte with little amounts of adhering cytoplasm are continuously recorded and have been shown to occur, steadily and gradually build up cellular structures by self-organization and self-assembly. Up to the present, we have cultured these kinds of cellular organizations repeatedly. Therefore, it can be concluded that the existence of cell reformation on the basis of yolk granules according to the dynamic morphological changes is an objective reality.