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At least 19 recordsLinked to original sources

Implantation and development of the gut flora in the newborn animal.

The newborn mammal, germfree in the mother's uterus, steps in complex microbial environment as soon as born. Bacterial development in the digestive cavities of the newborn animal, from the environmental bacteria, occurs very quickly. Within three hours after birth a small microbial population is present in the piglet, baby mouse or human baby. Within twelve hours after birth, dominant microbial population of the newborn animal can be as important as that of the adult animal. In any case, this highest level is reached within 24 h after birth. Studying several animal species, one observes a certain diversity in the steps of establishment of the principal bacterial groups. For instance, facultative anaerobic bacteria appear before strictly anaerobic bacteria in the young mouse, whereas the opposite situation happens in the young hare. In the calf and the piglet, strictly and facultative bacteria establish approximatively at the same time. On day one after birth E. coli and Streptococci establish in the human infant, and also species belonging to genus Bacteroides and Bifidobacterium. This last genus becomes dominant from 4 to 5 days after birth. The newborn successively meets three different bacterial ecosystems: maternal vagina, maternal feces and finally environment where it is reared. Each of these three ecosystems probably takes a role in the elaboration of the newborn animals flora, but in proportion difficult to estimate. Any way, one can state that the newborn possess powerful systems to sort out certain specific bacterial species among those constituting the environmental population to which he is exposed.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

[Evaluation of the adhesion, colonization and enterotoxigenicity of Vibrio cholerae in the enteral infection of intact and passively immunized newborn animals].

V. eltor were introduced into 323 suckling rabbits through a gastro-duodenal tube and into 629 suckling mice either by the same method, or per annum by a new specially developed technique. Passive immunization was achieved in suckling mice by the preliminary introduction of antibacterial sera into the small intestine or by feeding them with the milk of female mice immunized at the end of pregnancy, and in suckling rabbits by feeding them with the milk of goats immunized by introducing vibrios through the tests of the udder. To evaluate the results, the accumulation of liquid in the intestine and the development of diarrhea were taken into account, quantitative inoculation of homogenized intestinal matter was made; vibrios on the epithelium of the villi in the small intestine were counted and the changes of enterocytes and the lamina propria, observed in light and electron microscopy, were considered. The results of the complex quantitative evaluation in intact suckling animals revealed that the enterotoxigenicity of vibrios was manifested after their adhesion to and later colonization on the intestinal epithelium. Passive antibacterial immunization suppressed their adhesion and colonization, which resulted in protection from the enterotoxigenic effect of vibrios and their elimination from the intestine.

Animals↗

[Experimental candidiasis of the digestive organs in newborn animals].

Morphogenesis of alimentary tract candidosis was studied in the experimental neonate model. The infection was characterized by rapid progression, multiorgan involvement and weak cellular responses. Most commonly the oral cavity and esophagus were the sites of superficial lesions, while the stomach of deep ones. The penetration of the mucous membrane by fungal elements and the vascular invasion resulted in some cases in hematogenous dissemination of the infection.

Animals↗

Intestinal absorption of colostral lymphoid cells in newborn animals.

Intestinal absorption of colostral lymphoid cells was studied in 23 piglets of four sows and 17 lambs of ewes. From the colostrum and blood of the dams the lymphoid cells were isolated with Ficoll-Paque and labelled with technetium (Na99mTcO4). In the 7th hour after birth, 10 ml volume of the cell suspensions (piglets: 10(7) cells, lambs: 5 x 10(7) cells) were injected, following laparotomy, directly into the stomach or into the jejunum, or through a nasooesophageal tube. Cryostat sections of duodenum, jejunum and lymph node samples of animals were examined by autoradiography. It was found that lymphoid cells present in the colostrum of a piglet and lamb of their own mother were absorbed from the digestive tract and, via the lymphatic vessel, were transported to the mesenteric lypmph nodes. Electron microscopy revealed that absorption takes place intercellularly. Colostral cells of sows other than a piglet's own mother (allogeneic cells), the lymphoid cells isolated from the blood and heat-treated colostral lymphoid cells were not absorbed. The immunization of ewes and their lambs by tetanus anatoxin demonstrate, that the absorbed lymphoid cells remain immunologically active, and may transfer immune information to the lambs.

Animals↗

[Inhalation of organic solvents during the last third of pregnancy in Sprague-Dawley rats. Somatometric and cerebellar consequences in newborn animals].

Cerebellar morphogenesis as well as somatometric parameters of progenies from mothers exposed to ethyl-ether, chloroform, turpentine or thinner were registered a 24, 48 and 7 hours of age. 1. Mortality rate of 20 and 59% was observed in progenies of thinner or turpentine exposed mothers, correspondingly. 2. Delay of intrauterine growth manifested by body weight, size and cephalic diameter was evident in chloroform exposed groups (P < 0.01). 3. Cerebellar maturation delay was found in thinner or turpentine prenatally exposed litters. 4. The number of Purkinje cells was significantly reduced in ethyl-ether and chloroform exposed groups (P < 0.01). These cells were found less affected by thinner or turpentine exposure (P < 0.01).

Abnormalities, Drug-Induced↗