scholarly journals THE COLONY MORPHOLOGY OF TUBERCLE BACILLI

1936 ◽  
Vol 63 (1) ◽  
pp. 95-108 ◽  
Author(s):  
Kenneth C. Smithburn

The colony topography of tubercle bacilli is significantly affected by altering the pH of the culture medium on which the organisms are grown. Under the conditions of these experiments, avian tubercle bacilli produce two variants, rough and smooth. The former are most numerous on the most acid medium used (pH 6.0); the smooth colonies are obtained over a broad range of pH. Three colonial variants of bovine and human tubercle bacilli are described. Both mammalian types produce greater numbers of rough colonies at pH 6.0. The bovine type strains produce greatest numbers of smooth colonies in the pH range 6.4 to 6.8, and intermediate colonies on alkaline medium. The human type strains produce greatest numbers of smooth colonies at pH 6.4 and large numbers of intermediate colonies at pH 6.8 and pH 7.2. Included among the avian and bovine strains studied are organisms of widely varying pathogenic properties. Virulent and attenuated strains of a given type produce similar colonial variants under similar environmental conditions.

1929 ◽  
Vol 50 (6) ◽  
pp. 747-765 ◽  
Author(s):  
Max B. Lurie

In agreement with previous work (6) it was found that in normal rabbits after a primary inoculation of 0.01 mg. of human tubercle bacilli the organism shows a preliminary growth, which commences at once in all the organs, and reaches its height in the second week in the liver, spleen, and bone marrow; thereafter destruction begins, and is practically complete by the sixth week in the liver and bone marrow and less complete in the spleen. In the lung and kidney the largest number are isolated in the fourth week and thereafter there is a tendency to destruction, but to destruction far less complete than in the other organs, for even two months after infection large numbers of tubercle bacilli persist. Associated with this multiplication of the human tubercle bacilli were found extensive or moderate tuberculous lesions in the lung and kidney with moderate or slight changes in the liver, spleen and bone marrow. In contrast to these observations, it was found that in rabbits reinfected with the same quantity of human tubercle bacilli, the organism was destroyed immediately without any preliminary multiplication in the liver, spleen and bone marrow, though a few bacilli persisted in these organs even two months after reinfection. Neither could definite evidence of multiplication of the tubercle bacilli of reinfection in the lung and kidney of these rabbits be obtained; although variable and at times very large numbers of tubercle bacilli persisted in these organs, probably due to the primary infection. Nor were tuberculous changes found in any of the organs due to reinfection. Again in rabbits that received a primary inoculation of 0.01 mg. of bovine tubercle bacilli the organism multiplied in all the organs. This multiplication reached its height in the liver, spleen and bone marrow between the fourth and sixth week, instead of in the second week as with human bacilli. Thereafter destruction was practically complete in the liver and much less complete in the spleen and bone marrow; in the lung and kidney multiplication continued unabated to the second month. Associated with these bacteriological data, there developed a massive pulmonary tuberculosis with extensive or moderate disease in the kidney, spleen, bone marrow and liver. In rabbits reinfected with the same quantity of bovine tubercle bacilli after a primary infection with human tubercle bacilli, the organism, in all but a few instances, was destroyed immediately in the liver, spleen and bone marrow. Here again, with the bovine type as with the human type, after reinfection as after primary infection, the destruction was not quite complete and a few isolated bacilli persisted even two months after reinfection. As to the lung and kidney, evidence was obtained that the variable and at times very large numbers of tubercle bacilli that were found in these organs were of human type in their cultural characteristics, and that in these organs also, the bovine tubercle bacilli of reinfection failed to grow. There was also as a rule complete absence of any tuberculous lesions in the liver, spleen and bone marrow. Nor were there any tuberculous changes found in the lung and kidney due to the reinfection, but those variable residual lesions that were found were present before reinfection, as shown in the lung by x-ray photographs. There were a few instances in which restricted multiplication of the virus took place and slight tuberculous lesions developed after reinfection in rabbits in which the primary lesions had all but disappeared. Thus in rabbits having considerable residual lesions from a primary human infection the tubercle bacilli of reinfection, whether human or bovine, are destroyed immediately though incompletely without any preliminary multiplication. Yet these rabbits, which so efficiently destroy the more virulent bovine bacilli of reinfection introduced from without, at times harbor tremendous numbers of human tubercle bacilli in the old lesions of the lung and kidney. Parallel with the bacteriological and pathological studies of these rabbits, the serum of some of them was studied for the presence of circulating antibodies by McCutcheon, Strumia, Mudd (S), Mudd (E. B. H.) and Lucké (7). These investigators found that on primary infection there was only a slight and slowly developing production of agglutinating and phagocytosis-promoting antibodies whereas, in the reinfected rabbits, which showed an immediate destruction of the bacilli, these antibodies rose promptly and in relatively large amount. They suggest that the prompt rise of antibodies in reinfected animals may play a rôle in the immunity to tuberculosis. In the previous study, which was preformed in 1927, emphasis was placed upon the comparatively slower original rate of growth of the bovine bacillus in the rabbit as compared with that of the human type, and in this delay was seen a partial explanation of the greater virulence of the bovine organism for this species. The more rapid the original growth the more rapid was the following destruction. In this series of experiments, which were performed early in 1929, although the delayed destruction of the bovine type in the rabbit was amply confirmed, the original rate of growth is not any slower than the human type. Coincident with this increasingly more rapid rate of growth of the bovine bacillus in the body is a gradual decrease in the virulence of the organism. In 1925 and 1926 0.01 mg. of this bovine strain regularly killed rabbits in about 30 days after intravenous inoculation (8), but in this experiment none of the 3 rabbits died within 65 days after a similar infection and 2 rabbits were still living 110 days after injection.


1934 ◽  
Vol 60 (4) ◽  
pp. 515-540 ◽  
Author(s):  
W. Steenken ◽  
W. H. Oatway ◽  
S. A. Petroff

1. The H37 strain of human tubercle bacillus has been dissociated into two variants,—the R, or avirulent, and the S, or virulent, variants. 2. When their dissociation is complete, colony morphology for each is distinctive and typical. 3. The morphology of the individual bacilli of the two variants is different and characteristic. 4. The R variant develops best in an acid medium; the S develops best in an alkaline medium. 5. A method of assortment to facilitate the procedure of forced dissociation has been described. 6. The difference in virulence has been proven by observations on the pathogenesis of the variants.


1931 ◽  
Vol 53 (4) ◽  
pp. 535-552 ◽  
Author(s):  
Leslie T. Webster ◽  
Thomas P. Hughes

1. Pneumococci were obtained at one time or another from the nasal passages or throats of 80 per cent of 105 adults and children studied. In adults, they were obtained more frequently from the throat; in children, as often from the nasal passages as from the throat. 2. Of 500 pneumococcus strains studied, 97 per cent proved to be serologically specific. They formed smooth colonies and were for the most part avirulent for mice. Types I and II were obtained from one and two individuals respectively on one occasion only. Type III was obtained from nine individuals; Type XIII from nine individuals; Type XVI and Type XVIII from three individuals, for varying periods in each case. Atypical pneumococci were secured from 13 persons on single and scattered occasions. They varied in colony morphology, did not kill mice, or agglutinate in saline, but flocculated in all types of antipneumococcus sera employed and over a wide pH range in acid buffers. Their occurrence was apparently not associated with any type-transformation or virulence-enhancement process in vivo. 3. Strains of pneumococcus obtained on successive cultures from a given carrier were, with rare exceptions, of the same serological type and were similar in colony morphology, virulence for mice, and other tested biological characteristics. 4. Pneumococci of Types I and II were obtained under conditions suggestive that they lacked a capacity to spread readily; pneumococci of Types III and XIII, on the other hand, were obtained under conditions suggestive that they were spreading from person to person. 5. The persons studied differed consistently with respect to the occurrence of pneumococci. Some were pneumococcus-free, some were transient carriers, some periodic, and some chronic carriers. Data are given which suggest that the differences were due to variations in host resistance. 6. The incidence of pneumococci in all individuals studied underwent a seasonal variation paralleling that of coryza and sore throats in the same persons.


1977 ◽  
Vol 28 (4) ◽  
pp. 439 ◽  
Author(s):  
DW Morton ◽  
IAE Bayly

Fifty-three temporary freshwater pools (mean depth 23 cm) located mainly in eastern Victoria were studied from February to September 1973. Chemical parameters determined were pH (range 5.7-8.2, mean 6.9), conductivity (K18, range 55-5500, mean 340 �S/cm), dissolved oxygen (range 23-170, mean 72% saturation) and turbidity (range 2-310, mean 50 Formazin turbidity units). A total of 60 microcrustacean species was recorded. The Australasian endemic cladoceran, Saycia cooki (King), was of common occurrence from June through to August. The fact that it tends to reach peak numbers early in the life of a pool is probably related to the production of large numbers of ephippial eggs. In contrast, cladocera which produce only one or two ephippial eggs, such as Chydorus, Moina and Simocephalus, tend to appear later in succession. Simocephalus expinosus (benthic) and Daphnia carinata, s.l. (planktonic) had mutually exclusive distributions and are apparently unable to coexist in shallow waters. Endemic cyclopoid copepods encountered included three new species of Microcyclops, M. arnaudi (Sars), Acanthocyclops australis Sars, and Acanthocyclops, sp. nov. Like Saycia, Microcyclops varicans and Acanthocyclops bisetosus exhibited maximal numbers early in succession. Several new combinations of coexisting calanoid copepod species belonging to the genera Boeckella and Hemiboeckella are reported. Computer analysis showed that the following four groups of species had a high probability of co-occurrence: (1) Cypretta sp., Attheyella australica, Ilyodromus sp., Saycia cooki; (2) Cyprinotus leanus, Acanthocyclops bisetosus, Moina tenuicornis; (3) Boeckella major, B. pseudochelae, Cypris sp., Daphnia carinata, s.l. ; (4) Simocephalus exspinosus, Microcyclops varicans.


Genome ◽  
2006 ◽  
Vol 49 (4) ◽  
pp. 346-353 ◽  
Author(s):  
Ellen C Jensen ◽  
Jacob M Hornby ◽  
Nicole E Pagliaccetti ◽  
Chuleeon M Wolter ◽  
Kenneth W Nickerson ◽  
...  

Candida albicans is a diploid fungus that undergoes a morphological transition between budding yeast, hyphal, and pseudohyphal forms. The morphological transition is strongly correlated with virulence and is regulated in part by quorum sensing. Candida albicans produces and secretes farnesol that regulates the yeast to mycelia morphological transition. Mutants that fail to synthesize or respond to farnesol could be locked in the filamentous mode. To test this hypothesis, a collection of C. albicans mutants were isolated that have altered colony morphologies indicative of the presence of hyphal cells under environmental conditions where C. albicans normally grows only as yeasts. All mutants were characterized for their ability to respond to farnesol. Of these, 95.9% fully or partially reverted to wild-type morphology on yeast malt (YM) agar plates supplemented with farnesol. All mutants that respond to farnesol regained their hyphal morphology when restreaked on YM plates without farnesol. The observation that farnesol remedial mutants are so common (95.9%) relative to mutants that fail to respond to farnesol (4.1%) suggests that farnesol activates and (or) induces a pathway that can override many of the morphogenesis defects in these mutants. Additionally, 9 mutants chosen at random were screened for farnesol production. Two mutants failed to produce detectable levels of farnesol.Key words: farnesol-remedial mutants, farnesol-sensing mutants, farnesol-synthesis mutants, quorum sensing, Candida albicans, morphological transition.


1994 ◽  
Vol 353 ◽  
Author(s):  
S. Fukunaga ◽  
H. Yoshikawa ◽  
K. Fujiki ◽  
H. Asano

AbstractThe active range ofDesulfovibrio desulfuricans. a species of sulfate-reducing bacteria, was examined in terms of pH and Eh using a fermenter at controlled pH and Eh. Such research is important because sulfate-reducing bacteria (SRB) are thought to exist underground at depths equal to those of supposed repositories for high-level radioactive wastes and to be capable of inducing corrosion of the metals used in containment vessels.SRB activity was estimated at 35°C, with lactate as an electron donor, at a pH range from 7 to 11 and Eh range from 0 to -380 mV. Activity increased as pH approached neutral and Eh declined. The upper pH limit for activity was between 9.9 and 10.3, at Eh of -360 to -384 mV. The upper Eh limit for activity was between -68 and -3 mV, at pH 7.1. These results show that SRB can be made active at higher pH by decreasing Eh, and that the higher pH levels of 8 to 10 produced by use of the buffer material bentonite does not suppress SRB completely.A chart was obtained showing the active range ofDesulfovibrio desulfuricansin terms of pH and Eh. Such charts can be used to estimate the viability of SRB and other microorganisms when the environmental conditions of a repository are specified.


1987 ◽  
Vol 88 (5) ◽  
pp. 669-678
Author(s):  
P.L. McNeil ◽  
E. Warder

We describe and characterize an exceptionally rapid and simple new technique for loading large numbers of cultured cells with large macromolecules. The culture medium of the cell monolayer is replaced by a small volume of the macromolecule to be loaded. Glass beads (75–500 micron diameter) are then sprinkled onto the cells, the cells are washed free of beads and exogenous macromolecules, and ‘bead-loading’ is completed. The conditions for bead-loading can readily be modified to accommodate cell type and loading objectives: for example, the amount of loading per cell increases if bead size is increased or if beads are agitated after sprinkling onto the monolayer, but at the expense of increased cell loss. As many as 97% of a population of bovine aortic endothelial (BAE) cells were loaded with a 10,000 Mr dextran; and 79% with a 150,000 Mr dextran using bead-loading. Various cell lines have been loaded using glass beads. Moreover, bead-loading has the advantage of producing loaded cells that remain adherent and well-spread, thus minimizing recovery time and permitting immediate microscopic examination.


Plant Disease ◽  
1998 ◽  
Vol 82 (6) ◽  
pp. 631-638 ◽  
Author(s):  
Kenneth L. Conn ◽  
Edlira Leci ◽  
Giora Kritzman ◽  
George Lazarovits

A procedure is described for estimating Streptomyces populations in soil. Soils are air-dried, 10g quantities are shaken in plastic bags containing 0.1% water agar and homogenized with a Stomacher homogenizer, serial dilutions are plated on a semi-selective culture (STR) medium and incubated for 2 weeks at 22°C, and the Streptomyces colonies are enumerated. Use of STR medium reduced the bacterial and fungal colonies recovered from soil to levels below that of the Streptomyces spp. while not affecting the number of Streptomyces colonies compared with those enumerated on yeast malt extract medium. A procedure for screening large numbers of Streptomyces strains for thaxtomin production, a phytotoxin recognized as a virulence marker in S. scabies, is also described. Strains are grown on oatmeal medium, and the thaxtomin is extracted from the medium by facilitated diffusion and detected by miniature thin layer chromatography. S. scabies and S. acidiscabies strains (approximately 130 from Ontario and 70 from other locations in North America) that produced thaxtomin did not form aerial mycelia or sporulate on STR medium within 2 weeks at 22°C. Ontario S. scabies strains that produced thaxtomin A also produced melanin on STR medium. All S. scabies strains from scab lesions that produced thaxtomin A had this colony morphology, whereas only 4 to 9% of strains from soil with this colony morphology produced thaxtomin A. Using these procedures, we determined that the population of thaxtomin-producing S. scabies in soil from a potato field in Ontario with a history of potato scab was about 20,000 CFU/g soil.


1979 ◽  
Author(s):  
W.E. Laug

Cloned endothelial cells obtained from the aorta of 1-2 day old calves produced high fibrinolytic activity, which was 90% dependent upon the presence of plasminogen when grown on 125 I fibrin coated dishes. High plasminogen-dependent proteolytic activity was also demonstrated in the cell lysate and in the culture medium of the cells. The production and secretion of this prtitease were found to increase during the log phase of cell growth and to reach a maximum at con fluency. Thereafter they remained constantly high. This protease, partially purified from the culture medium of confluent endothelial cell cultures, is aiginine specific and activates plasminogen by piOteolytic cleavage to plasmin. Its proteolytic activity which is highest in the pH range of 7.5 to 8.0 is irreversibly inhibited by diisopropyl fluorophosphate, suggesting that it is a serine protease. The molecular weight of this protease is approximately S2000.


1938 ◽  
Vol 21 (5) ◽  
pp. 601-620 ◽  
Author(s):  
M. Kunitz

1. A powerful kinase which changes trypsinogen to trypsin was found to be present in the synthetic liquid culture medium of a mold of the genus Penicillium. 2. The concentration of kinase in the medium is increased gradually during the growth of the mold organism and continues to increase for some time even after the mold has ceased growing. 3. Mold kinase transforms trypsinogen to trypsin only in an acid medium. It differs thus from enterokinase and trypsin which activate trypsinogen best in a slightly alkaline medium. 4. The action of the mold kinase in the process of transformation of trypsinogen is that of a typical enzyme. The process follows the course of a catalytic unimolecular reaction, the rate of formation of a definite amount of trypsin being proportional to the concentration of kinase added. The ultimate amount of trypsin formed, however, is independent of the concentration of kinase used. 5. The formation of trypsin from trypsinogen by mold kinase is not accompanied by any measurable loss of protein. 6. The temperature coefficient of formation of trypsin from trypsinogen by mold kinase varies from Q5–15 = 1.70 to Q25–30 = 1.25 with a corresponding variation in the value of µ from 8100 to 4250. 7. Trypsin formed from trypsinogen by means of mold kinase is identical in crystalline form with the crystalline trypsin obtained by spontaneous autocatalytic activation of trypsinogen at pH 8.0. The two products have within the experimental error the same solubility and specific activity. A solution saturated with the crystals of either one of the trypsin preparations does not show any increase in protein concentration or activity when crystals of the other trypsin preparation are added. 8. The Penicillium mold kinase has a slight activating effect on chymo-trypsinogen the rate being only 1–2 per cent of that of trypsinogen. The activation, as in the case of trypsinogen, takes place only in an acid medium. 9. Mold kinase is rapidly destroyed when brought to pH 6.5 or higher, and also when heated to 70°C. In the temperature range of 50–60°C. the inactivation of kinase follows a unimolecular course with a temperature coefficient of Q10 = 12.1 and µ = 53,500. The molecular weight of mold kinase, as determined by diffusion, is 40,000.


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