Diversifications in the Tube Dilution Test for Antibiotic Sensitivity of Microorganisms

The tube dilution method of performing antibiotic sensitivity tests is commonly employed as an accurate method for defining the minimal inhibitory concentration in relation to pathogenic organisms. It is also used as a reference for comparing minimal inhibitory concentrations with the size of the zone of inhibition in the agar diffusion test. Although surveys have shown that there is no standardized method and technique of performing the tube dilution test, it is generally assumed that all of the diversified methods will yield the same results and interpretations. With the assistance of five experts, seven different tube dilution methods were compared; 16 antibiotics, and three organisms for each antibiotic, were used. The conclusions drawn are that, although the accuracy of a single method within its own confines is acknowledged, the minimal inhibitory concentrations and interpretations cannot be interpolated from one laboratory to another where a different technique is employed. The results are frequently discrepant. It is suggested that a uniform method be developed and promulgated for general use.     

Competition in Bembicium auratum (Gastropoda) and its effect on microalgal standing stock in mangrove muds

Summary Field experiments were undertaken on the intertidal gastropod Bembicium auratum, which is one of the dominant organisms in sheltered bays and mangroves in New South Wales. Animals were caged at various densities ranging from natural levels to about four times normal density. Increased density resulted in increased mortality (particularly of juveniles), reduced body weight, and (less conclusively) a decline in growth rate. Chlorophyll levels of the mangrove mud within the cages were monitored as an index of food availability, and increased rapidly in the control cages in the absence of Bembicium, remained steady at normal Bembicium densities, and declined at higher densities. Parallel experiments were conducted on the effects of substratum on Bembicium. One series of animals was allowed access to a hard substratum and the other only to mud. Body weights and survivorship were proportionally lower in animals deprived of a hard substratum. Juveniles were particularly susceptible to a shortage of food and more dependent on a hard substratum than adults. The population structure also suggests a high juvenile mortality but high adult survival and longevity. Bembicium is very abundant low on the shore but numbers decline and body weights increase higher up. Chlorophyll levels and amounts of hard substratum also decline up the shore. Possibly juveniles settle selectively (or survive better) low on the shore where oysters provide a dense hard substratum. Adults are less dependent on the hard substratum and may disperse up the shore, explaining the patterns of abundance and size.As Bembicium limits its own food supply and seemingly is limited by it, predation is unlikely to play an important role in restricting population density.     

Outpatient Termination of Pregnancy

Termination of pregnancies ranging from 6 to 10 weeks'' gestation is described in 127 women who attended the hospital as outpatients. The technique employed was to aspirate the products of conception through a narrow plastic tube using a high negative pressure. Infiltration of the cervix with local anaesthetic proved so effective that the procedure could be carried out on the fully conscious patient. The short time taken to evacuate the uterus, the small blood loss, and the low incidence of complications in the latter part of the study suggest that the technique is a valuable procedure. Relatively more women can be terminated as outpatients than as inpatients with a corresponding reduction in the demands made on gynaecological beds.     

Investigation of endosomal compartments involved in endocytosis and transcytosis of polymeric immunoglobulin A by subcellular fractionation of perfused isolated rat liver.

1. A gamma camera was used to monitor continuously the uptake of radiolabelled polymeric immunoglobulin A (pIgA) into the rat body after intravenous injection. Uptake into liver was fast but, since the peak of liver labelling occurred only after 9-15 min, it was not sufficiently rapid to constitute a pulse dose. A perfused, isolated rat liver system was therefore established which could be given a single pass dose of pIgA; a variety of tests showed such livers remained viable for at least 3 h and could be subsequently fractionated on Ficoll and Nycodenz gradients with normal distributions of marker enzymes. 2. Subcellular fractionation at different times after a single pass dose of pIgA showed that whilst pIgA appeared sequentially in sinusoidal plasma membrane, light endosomes, dense endosomes, very dense endosomes and lysosomes as in vivo, the predominance of pIgA in the light endosome compartment disappeared much earlier than after injection in vivo of pIgA, presumably because this compartment was not being continuously loaded over the first 10-15 min. The time course of appearance of label in bile was unchanged. A large excess of unlabelled asialofetuin did not change these patterns, indicating that the asialoglycoprotein receptor was not involved. 3. Low doses of the microtubule agent colchicine reduced the proportion of pIgA reaching the bile, but subcellular fractionation of treated liver showed that distribution of label amongst liver fractions was little changed, although the overall liver pIgA content had increased. This would suggest that pIgA did not remain in the common compartment which could have supplied bile or lysosomes but rather flowed out of it as rapidly as in untreated liver but towards those compartments supplying the lysosomes. 4. Experiments with nocodazole, which reversibly disrupts microtubules, showed that very little of the pIgA taken into an inhibited liver appeared in the bile after nocodazole was removed 30 min later, even though a second dose of pIgA, given after nocodazole removal, appeared in bile with a normal time course. The first dose of pIgA must therefore have passed beyond the compartments competent to supply the bile before nocodazole was removed. Such compartments were undamaged since the second dose of pIgA appeared in bile normally. We therefore conclude that the bulk of pIgA must be supplied to the bile from light or dense endosomes rather than from very dense endosomes and lysosomes.