PubMed · 4374695
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
H E Meyer. 1974-12-17. [Amebiasis].. https://pubmed.ncbi.nlm.nih.gov/4374695/
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
A cell-free growth medium for the opportunistic pathogenic ameba Balamuthia mandrillaris is presented. This represents an advance over the use of monkey kidney cells for growth of the amebas and can be helpful in isolation of these amebas from brain tissue from cases in which amebic meningoencephalitis is a diagnostic possibility, as well as for biochemical and molecular biological studies. Three isolates of Balamuthia have been cultured in this medium. The cell-free growth system was also used to screen cultures for sensitivity to a variety of antimicrobial agents. Of the various drugs tested, pentamidine isethionate was most effective against amebas (ca. 90% inhibition after 6 days of exposure), but the drug was amebastatic and not amebacidal in the axenic system at the highest concentration tested (10 micrograms/ml).
In the protozoan parasite Entamoeba histolytica (which causes amoebiasis in humans), the rRNA genes (rDNA) in the nucleus are carried on an extrachromosomal circular plasmid. For strain HM-1:IMSS, the size of the rDNA plasmid is 24.5 kb, and 200 copies per genome are present. Each circle contains two rRNA transcription units as inverted repeats separated by upstream and downstream spacers. We have studied the replication of this molecule by neutral/neutral two-dimensional gel electrophoresis and by electron microscopy. All restriction fragments analyzed by two-dimensional gel electrophoresis gave signals corresponding to simple Y's and bubbles. This showed that replication initiated in this plasmid at multiple, dispersed locations spread throughout the plasmid. On the basis of the intensity of the bubble arcs, initiations from the rRNA transcription units seemed to occur more frequently than those from intergenic spacers. Multiple, dispersed initiation sites were also seen in the rDNA plasmid of strain HK-9 when it was analyzed by two-dimensional gel electrophoresis. Electron microscopic visualization of replicating plasmid molecules in strain HM-1:IMISS showed multiple replication bubbles in the same molecule. The location of bubbles on the rDNA circle was mapped by digesting with PvuI or BsaHI, which linearize the molecule, and with SacII, which cuts the circle twice. The distance of the bubbles from one end of the molecule was measured by electron microscopy. The data corroborated those from two-dimensional gels and showed that replication bubbles were distributed throughout the molecule and that they appeared more frequently in rRNA transcription units. The same interpretation was drawn from electron microscopic analysis of the HK-9 plasmid. Direct demonstration of more than one bubble in the same molecule is clear evidence that replication of this plasmid initiates at multiple sites. Potential replication origins are distributed throughout the plasmid. Such a mechanism is not known to operate in any naturally occurring prokaryotic or eukaryotic plasmid.
Individuals from 13 wild mammalian species collected in southwestern Tennessee were serologically positive for anti-Naegleria spp. antibodies (ANA). This is the first report of ANA in wild mammals. Interspecific differences in the occurrence of ANA and titers indicate that wild mammals have differing degrees of contact with Naegleria spp. based on ecological or behavioral adaptations, and possibly the innate ability of a species to produce ANA. Intraspecifically, it appears that if a mammal is exposed to Naegleria spp. in the environment, titers of ANA will not significantly differ, regardless of age or sex. Adults of many species had significantly higher occurrences of ANA. Populations of juvenile wild mammals are probably at higher risk than adults to naeglerial infection in the environment, not because of lower titers, but because their chance of having ANA is less than adults. Differences in the occurrence of ANA in wild mammals may also reflect how humans are exposed to Naegleria spp. in the environment.