Suppression of Trypanosoma congolense, T. vivax and T. brucei infection rates in tsetse flies maintained on goats immunized with uncoated forms of trypanosomes grown in vitro

Parasitology ◽  
1985 ◽  
Vol 91 (1) ◽  
pp. 53-66 ◽  
Author(s):  
M. Murray ◽  
H. Hirumi ◽  
S. K. Moloo

Significant suppression in the incidence of cyclical development of Trypanosonia congolense, T. vivax and T. brucei occurred in Glossina morsitans centralis maintained on goats immunized with in vitro-propagated uncoated forms of T. congolense, T. vivax and T. brucei, respectively. This was observed when tsetse given a T. congolense-infected feed were subsequently maintained on uninfected immunized goats and also when uninfected tsetse were fed on immunized goats infected with T. congolense, T. vivax and T. brucei. Suppression of infection rates in tsetse was trypanosome species specific, but was independent of the trypanosome stock used for immunization of goats. These findings were reflected in antibody responses to uncoated trypanosomes, as measured by immunofluorescence and the solid-phase immuno radiometric binding assay. Thus, antibody from goats immunized with uncoated trypano somes of one species exhibited minimal reactivity with uncoated forms of other species of trypanosomes, but showed high levels of activity with uncoated forms of the same or unrelated stocks of the same species. However, in view of the range of hosts upon which tsetse feed, it is open to question whether the use of a vaccine which suppresses trypanosome infection rates in tsetse would have any significant effect in the field.

1969 ◽  
Vol 58 (3) ◽  
pp. 537-548 ◽  
Author(s):  
D. A. T. Baldry

The distribution and trypanosome infection rates ofGlossina morsitans submorsitansNewst. were studied during the wet season of 1967 along 75 miles of the main trade cattle route which passes through the savannah country between Ilorin and Oyo in south-western Nigeria.G.m. submorsitanswas found inhabiting open woodland, grassland, farmland and the environs of towns associated with the cattle route. In comparison with the types of habitat this species occupies in its zone of wide distribution in northern Nigeria, those habitats studied were considered atypical. It is suggested that the presence ofG.m. submorsitansin the area investigated had resulted from a southward population advance over the last 50 years and this hypothesis is discussed in relation to existing knowledge ofG.m. submorsitansadvances.The trypanosome infection rates of 61.6 and 76.6 per cent, found in 364 examples ofG.m. submorsitansdissected are much higher than previously recorded for any of the subspecies ofG. morsitansWestw. A steady southward increase in the trypanosome infection rates ofG.m. submorsitanswas demonstrated for populations inhabiting 200 miles of cattle route. Trypanosome infections inG.m. submorsitansare attributed toTrypanosoma vivaxandT. congolense, and the absence ofbrucei-group infections is discussed in relation to the incidence ofT. bruceiinfections in trade cattle and limitations of the technique used for demonstrating infections in tsetse flies.It is stressed that epizootiological aspects of the present findings cannot be clarified until reliable data on trypanosome infections of trade cattle in the area studied are available.


1986 ◽  
Vol 23 (6) ◽  
pp. 661-667 ◽  
Author(s):  
J. A. Ellis ◽  
S. Z. Shapiro ◽  
O. Ole Moi-Yoi ◽  
S. K. Moloo

Rabbits exposed to feeding tsetse flies developed cutaneous hypersensitivity responses to fly bites. These responses had characteristics of immediate and delayed type hypersensitivity. Saliva components from the tsetse fly Glossina morsitans centralis were electrophoretically separated by sodium dodecyl sulfate-poly-acrylamide gel electrophoresis. Major salivary proteins of 160, 92, 66, 64, 55, 42, 33, 28, and 15 kilodaltons were identified. Separated salivary components were transferred to nitrocellulose filters and probed with lectins and with whole sera and purified IgG from rabbits which had been exposed, via fly feeding, to tsetse antigens for variable periods. Many of the salivary proteins were identified as glycoproteins. Several major salivary proteins were recognized by antibodies from sensitized rabbits.


1997 ◽  
Vol 41 (7) ◽  
pp. 1604-1606 ◽  
Author(s):  
A S Peregrine ◽  
M A Gray ◽  
S K Moloo

Resistance to isometamidium was increased 94-fold in a clone of Trypanosoma congolense (clone IL 1180) by repeated subcurative treatment of infected mice for 11 months. This was associated with 3.4-, 33-, and 4.2-fold increases in resistance to diminazene, homidium, and quinapyramine, respectively. Both T. congolense IL 1180 and the resistant derivative were able to undergo cyclical development in Glossina morsitans centralis tsetse flies, producing hypopharyngeal infection rates of 40.0 and 39.8%, respectively.


Parasitology ◽  
1993 ◽  
Vol 107 (2) ◽  
pp. 141-145 ◽  
Author(s):  
S. C. Welburn ◽  
K. Arnold ◽  
I. Maudlin ◽  
G. W. Gooday

SUMMARYRickettsia-like organisms (RLO) from tsetse midguts and mosquito cell cultures showed high levels of endochitinase activity. A line of Glossina morsitans morsitans highly susceptible to midgut trypanosome infection and with high incidence of RLO infection showed significantly greater chitinolytic activity than G. austeni which had low RLO incidence and were correspondingly refractory to midgut infection. Midgut infection rates of Trypanosoma brucei rhodesiense in G. m. morsitans showed a dose-related increase when flies were fed N-acetyl-D-glucosamine (GlcNAc) in the infective meal and for 4 subsequent days. A model is proposed for susceptibility to trypanosome infection based on the generation of GlcNAc by RLO endochitinase activity in tsetse pupae inhibiting midgut lectin in teneral flies.


Parasitology ◽  
1991 ◽  
Vol 102 (2) ◽  
pp. 193-199 ◽  
Author(s):  
M. K. Shaw ◽  
S. K. Moloo

SUMMARYThe midgut epithelium ofGlossina morsitans centralis, G. austeni, G. pallidipes, G. palpalis palpalis, G. p. gambiensis, G. fuscipes fuscipes, G. tachinoidesandG. brevipalpisfrom ILRAD-bred colonies was examined, by electron microscopy, for the presence and distribution of Rickettsia-like organisms (RLOs). RLOs were present in the midgut epithelial cells of all non-teneral tsetse. InG. m. centralis, G. pallidipesand, to a much lesser extent,G. brevipalpis, RLOs were numerous and were present in all the specimens examined. RLOs were present in fewer numbers in the epithelial cells of tenerals of these three tsetse species. In contrast, RLOs occurred in very much lower numbers within the midgut cells of nonteneralG. austeni, G. p. palpalis, G. p. gambiensis, G. f. fuscipesandG. tachinoides; were not seen in every specimen, and were rarely observed in the midgut cells of teneral tsetse. The RLOs were typical rod-shaped bacteria with an inner and outer membrane, which occurred free within the host cell cytoplasm and appeared to cause no obvious pathology. The micro-organisms divided by binary fission and at least two distinct morphological forms plus a range of intermediate forms were seen in the midgut cells. A comparison of the presence and numbers of RLOs within the midgut cells and the midgut infection rates of bothTrypanosoma congolenseandT. b. brucei, both betweenGlossinaspecies and also within the same stock of tsetse, clearly indicates that the ability of trypanosomes to establish and develop to mature infections is unlikely to be correlated solely with the presence of RLOs within the tsetse midgut.


2020 ◽  
Author(s):  
Robert Opiro ◽  
Robert Opoke ◽  
Harriet Angwech ◽  
Esther Nakafu ◽  
Francis A. Oloya ◽  
...  

Abstract Background: African trypanosomiasis, caused by protozoa of the genus Trypanosoma and transmitted by the tsetse fly, is a serious parasitic disease of humans and animals. Reliable data on the vector distribution, feeding preference and the trypanosome species they carry is pertinent to planning sustainable control strategies.Methodology: We deployed 109 biconical traps in 10 villages in two districts of northwestern Uganda to obtain information on the apparent density, trypanosome infection rates and blood meal sources of tsetse flies. A subset (272) of the collected samples was analyzed for detection of trypanosomes species and sub-species using a nested PCR protocol based on primers amplifying the Internal Transcribed Spacer (ITS) region of ribosomal DNA. 34 blood-engorged adult tsetse midguts were analyzed for blood meal sources by sequencing of the mitochondrial cytochrome c oxidase 1 (COI) and cytochrome b (cytb) genes. Results: Out of the 109 traps deployed, we captured 622 Glossina fuscipes fuscipes tsetse flies (269 males and 353 females). Apparent density (AD) ranged from 0.6 to 3.7 flies/trap/day in the two districts. 29 (10.7%) of the flies were infected with one or more trypanosome species. Infection rate was not significantly associated with neither age group (χ2 = 5.001, df=2, 0.082), sex of the fly (χ2 = 0.099, df = 1, p = 0.753), district of origin (χ2= 0.629, df = 1, p = 0.428) nor village (χ2= 9.252, df = 9, p = 0.414). Nested PCR revealed several species of trypanosomes: T. vivax (6.62%), T. congolense (2.57%), T. brucei and T. simiae each at 0.73%. Blood meal analyses revealed five principal vertebrate hosts, namely, cattle (Bos taurus), humans (Homo sapiens), Nile monitor lizard (Varanus niloticus), African mud turtle (Pelusio schapini) and the African Savanna elephant (Loxodonta africana).Conclusion: We found an infection rate of 10.78 %, with all infections attributed to trypanosome species that are causative agents for the animal disease only. However, more verification of this finding using large-scale passive and active screening of human and tsetse samples should be done. Cattle and humans appear to be the most important tsetse hosts in the region and should be considered in the design of interventions.


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