The influence of abiotic factors on the distribution of Biomphalaria pfeifferi (Krauss, 1848) (Planorbidae: Mollusca) and its lifecycle in South-Eastern Africa
- Authors: Appleton, Christopher Charles
- Date: 1976
- Subjects: Schistosomiasis , Mollusks as carriers of disease
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: vital:5835 , http://hdl.handle.net/10962/d1009495 , Schistosomiasis , Mollusks as carriers of disease
- Description: Previous studies on the influence of abiotic factors on the distribution of bilharzia intermediate host snails of the family Planorbidae are reviewed. Much of this work is basically descriptive and relatively few attempts have been made to examine the effects of these factors on snails in their natural habitats - to identify the factors precisely and to measure their critical levels. An account is given of recent studies on Eiomphalaria pfeifferi (Krauss) in two climatically different regions of southeastern Africa, at 6S5m altitude on the eastern Transvaal escarpment and 19m on the coastal peneplain of northern Zululand. These have shown the species to undergo a similar annual life-cycle of three overlapping generations in both areas. Further, in these areas where the snail has a discontinuous distribution, two abiotic factors, stream geology and water temperature, were found to be important in limiting its distribution. The longitudinal distribution of B. pfeifferi and another host snail Bulinus (Physopsis) globosus (Morelat), extended upstream in a perennial watercourse, the Gladdespruit, on the escarpment only as far as permanently lentic habitats were available. These habitats, usually detached from the channel, characterized the stream's lowest physical zone with its substratum of exposed granite, as opposed to the sandy-bottomed lotic zones upstream. The limit of the snails' occurrence lay close to the junction of these two substratum types. Granite is resistant to erosion but contains soft inclusions which erode more quickly than the hard matrix causing uneven weathering. This results in the formation of depressions in the stream bed (i.e. pools, potholes and backwaters) which provide the permanently lentic conditions necessary for the snails' survival. Temperature recordings made on this plain, upstream of the snails' limit, suggest that the water temperature here exceeded the critical lower levels required for a positive intrinsic rate of natural increase sufficiently often to permit the species to survive here, though not optimally. Above this point however, current velocities are continually in excess of the maximum tolerated (0.3 m/sec.) so that in this situation at least, current velocity is a dominant factor. A contrasting situation exists on the coastal peneplain of northern Zululand where B. pfeifferi occurs in some lentic habitats and not in others. This discontinuous distribution is shown to be related to the prolonged duration of temperatures above the level for optimal increase. The apparently suitable habitats from which B. pfeifferi was absent were found to be both very shallow and to experience these prolonged high temperatures during spring and early summer. This corresponds to the maturation period of the B. pfeifferi 1st generation as defined by Appleton (1974) and causes reduced fecundity probably through impaired gonad development. The density of its filial (2nd) generation is correspondingly reduced. A statistically significant partial-correlation (at a 1% level) was found between the fecundity of the 1st generation and increasing periods of temperatures above the species' optimal limit in the habitats involved during its maturation period (spring). It is interesting to nate here that B. (Ph.) globosus, which is known to be better adapted to high temperatures than B. pfeifferi (Shiff & Husting, 1966) occurred in all the waterbodies concerned. Both these factors therefore play important roles in determining the country-wide distribution pattern of the host snails. This distribution is closely correlated with the availability of permanently lentic habitats. In river systems, which form the main environment for these snails, such stable habitats occur almost entirely in low-gradient reaches over hard bed-rock which is resistant to erosion. Current velocities above 0.3 m/sec. render steeper reaches and those over soft, non-resistant rock and sand (unstable substrata) unsuitable and therefore constitute a most important limiting factor. Temperature however becomes a dominant factor in permanently lentic waterbodies. Biomphalaria pfeifferi is adversely affected by high temperature regimes and where such regimes occur in waterbodies which are too shallow to permit temperature gradient to develop, the species cannot survive whereas B. (Ph.) globosus can do so. This intolerance of high temperature regimes on the part of B. pfeifferi accounts for the species' adoption of a discontinuous distribution over the coastal plain of south-eastern Africa. A comparable pattern has been reported for the species over this plain northwards to approximately 16°S latitude in Mozambique and is probably due to a similar high-temperature effect. Further northwards in equatorial latitudes B. pfeifferi is restricted to the more elevated and cooler areas above an altitude of 500 - 600 m, probably because the very high temperature regimes prevailing in the lowlands there exclude the species altogether.
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- Date Issued: 1976
Isolation, identification and genetic characterisation of a microsporidium isolated from the carob moth, Ectomyelois ceratoniae (Lepidoptera: Pyralidae)
- Authors: Lloyd, Melissa
- Date: 2018
- Subjects: Pyralidae , Pyralidae -- Genetics , Pyralidae -- Phylogeny , Pyralidae -- Pathogens , Cladistic analysis , Transmission electron microscopy , Carob moth (Ectomyelois ceratoniae)
- Language: English
- Type: text , Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10962/61894 , vital:28075
- Description: Carob moth, Ectomyelois ceratoniae (Zeller) (Lepidoptera: Pyralidae) is an economically important pest, yet its biology and pest status on citrus in South Africa was, until recently, poorly understood. A study was initiated to determine the cause of collapse of a laboratory carob moth colony that was established to investigate the biology of carob moth on citrus and to develop integrated management strategies for the pest. An organism was isolated from deceased larvae and was morphologically identified as a microsporidium, based on transmission electron microscopy. Microsporidia are obligate intracellular parasites that have been found to infect almost all eukaryotes. Several Nosema species have been isolated from economically important insect pests, yet little genetic information is available from online databases for identification. Mature spores were recovered and measured using transmission electron microscopy. Spores were ovocylindrical with a wrinkled exospore, and had a length of 2.8 ± 0.02 pm and a width of 1.6 ± 0.04 pm. The identity of the microsporidium was confirmed by PCR amplification, sequencing and analysis of the regions encoding the ribosomal RNA. BLAST analysis of the different rRNA regions amplified showed that the microsporidium shared a 96 - 99 % identity with Nosema sp. M-Pr, Nosema carpocapsae, Nosema oulemae, Nosema sp. CO1, Microsporidium 57864, and Nosema bombi. Phylogenetic analysis of the SSU and LSU rRNA genes showed that the microsporidium clustered with the Nosema / Vairimorpha clade, supported by a bootstrap value of 100. The organisation of the RNA cistron was determined by PCR amplification using the primer set 18f and L1328r to be 5’-SSU-ITS-LSU-IGS-5S-3’, which confirms the placement of the microsporidium within the Nosema / Vairimorpha clade. Because the BLAST results showed a close relationship with Nosema carpocapsae, a microsporidium infecting codling moth, the pathogenicity of the microsporidium was tested against codling moth by inoculating artificial diet with a high spore concentration of 1.1 x 107 spores/ml and a low spore concentration of 1.1 x 104 spores/ml. DNA was extracted from deceased larvae inoculated with the high concentration, and PCR of the SSU rRNA gene and bacterial 16S region was performed. Mortality in the high concentration experiment was significant (p = 0.05), but the cause of infection was determined to be a bacterium, through sequencing and BLAST analysis of the bacterial 16S rDNA. The bacterium shared a 99 % identity with Bacillus cereus. Percentage mortality (p = 0.09), larval mass (p = 0.09) and instar (p = 0.24) did not differ significantly between treatments in the low concentration experiment. DNA was extracted from the larvae and PCR amplification of the SSU rRNA gene was performed to determine whether microsporidia were present. No SSU bands were observed in any of the treatments and percentage mortality was not significant, thus it was determined that no infection occurred. This is the first study to report the genetic characterisation of a microsporidium isolated from carob moth and provides important genetic information for classification of microsporidia within the Nosema / Vairimorpha clade. It is also one of few studies in which the complete rRNA cistron of a species within the Nosema / Vairimorpha clade has been sequenced. The identification of a microsporidium from a laboratory colony of carob moth is important as it provides information about pathogens infecting the carob moth and constraints to carob moth rearing, which is useful for further studies on rearing carob moth and for establishment of a clean colony for research purposes.
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- Date Issued: 2018