scholarly journals TrypanosomaInfection Rates inGlossinaSpecies in Mtito Andei Division, Makueni County, Kenya

2015 ◽  
Vol 2015 ◽  
pp. 1-8
Author(s):  
Daniel Mutiso Nthiwa ◽  
David O. Odongo ◽  
Horace Ochanda ◽  
Samoel Khamadi ◽  
Bernard M. Gichimu
Keyword(s):  
Infection Rate ◽  
Gel Electrophoresis ◽  
Internal Transcribed Spacer ◽  
Tsetse Fly ◽  
Transmission Risk ◽  
Agarose Gel Electrophoresis ◽  
Infection Rates ◽  
Pcr Assay ◽  
Internal Organs ◽  
Animal Trypanosomiasis

African Animal Trypanosomiasis (AAT) transmitted cyclically by tsetse fly (Glossinaspp.) is a major obstacle to livestock production in the tropical parts of Africa. The objective of this study was to determine the infection rates of trypanosomes inGlossinaspecies in Mtito Andei Division, Makueni County, Kenya. Tsetse fly species,G. longipennisandG. pallidipes, were trapped and DNA was isolated from their dissected internal organs (proboscis, salivary glands, and midguts). The DNA was then subjected to a nested PCR assay using internal transcribed spacer primers and individual trypanosome species were identified following agarose gel electrophoresis. Out of the 117 flies trapped in the area 39 (33.3%) were teneral while 78 (67%) were nonteneral.G. pallidipesconstituted the largest percentage of 58% whileG. longipenniswere 42%. The overall trypanosomes infection rate in all nonteneralGlossinaspp. was 11.53% withG. longipennisrecording the highest infection rate of 23.08% whileG. pallidipeshad an infection rate of 5.77%.T. vivaxwas the most infectious (10.26%) compared toT. congolense(1.28%). Mean apparent densities were strongly positively correlated with infection rates (r=0.95) confirming the importance of this parameter as an indicator of AAT transmission risk.

scholarly journals Apparent density, trypanosome infection rates and host preference of tsetse flies in the sleeping sickness endemic focus of   Northwestern Uganda

2020 ◽  
Author(s):  
Robert Opiro ◽  
Robert Opoke ◽  
Harriet Angwech ◽  
Esther Nakafu ◽  
Francis A. Oloya ◽  
...  
Keyword(s):  
Infection Rate ◽  
Apparent Density ◽  
Blood Meal ◽  
Nested Pcr ◽  
Tsetse Fly ◽  
Tsetse Flies ◽  
Trypanosome Species ◽  
Trypanosome Infection ◽  
Infection Rates ◽  
Monitor Lizard

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.

scholarly journals Apparent density, trypanosome infection rates and host preference of tsetse flies in the sleeping sickness endemic focus of Northwestern Uganda

2020 ◽  
Author(s):  
Robert Opiro ◽  
Robert Opoke ◽  
Harriet Angwech ◽  
Esther Nakafu ◽  
Francis A. Oloya ◽  
...  
Keyword(s):  
Infection Rate ◽  
Apparent Density ◽  
Blood Meal ◽  
Nested Pcr ◽  
Large Scale ◽  
Tsetse Fly ◽  
Tsetse Flies ◽  
Trypanosome Species ◽  
Infection Rates ◽  
Monitor Lizard

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, 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%), and 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 a moderately high infection rate of 10.78%, with all infections attributed to trypanosome species that are causative agents for the animal disease only. However, more validation 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.

scholarly journals Apparent Density, Trypanosome Infection Rates and Host Preference of Tsetse Flies in the Sleeping Sickness Endemic Focus of North-Western Uganda

2020 ◽  
Author(s):  
Robert Opiro ◽  
Robert Opoke ◽  
Harriet Angwech ◽  
Esther Nakafu ◽  
Francis A. Oloya ◽  
...  
Keyword(s):  
Infection Rate ◽  
Apparent Density ◽  
Blood Meal ◽  
Nested Pcr ◽  
Tsetse Fly ◽  
Tsetse Flies ◽  
Trypanosome Species ◽  
Trypanosome Infection ◽  
Infection Rates ◽  
Monitor Lizard

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 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, with infection rate significantly associated with age group (χ2 = 29.733, df = 2, p < 0.05) but not with sex (χ2 = 0.43, df = 1, p = 0.835) and district of origin (χ2 = 1.374, df = 1, p = 0.241). Nested PCR revealed several species of trypanosomes: T. vivax (62.1%), T. congolense (24.14 %), and T. brucei and T. simiae each at 6.89%. 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 a moderately high infection rate at 10.78%, with all infections attributed to trypanosome species that are causative agents for the animal disease only. However, more validation 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.

scholarly journals Apparent density, trypanosome infection rates and host preference of tsetse flies in the sleeping sickness endemic focus of Northwestern Uganda

2020 ◽  
Author(s):  
Robert Opiro ◽  
Robert Opoke ◽  
Harriet Angwech ◽  
Esther Nakafu ◽  
Francis A. Oloya ◽  
...  
Keyword(s):  
Infection Rate ◽  
Apparent Density ◽  
Blood Meal ◽  
Nested Pcr ◽  
Tsetse Fly ◽  
Tsetse Flies ◽  
Trypanosome Species ◽  
Trypanosome Infection ◽  
Infection Rates ◽  
Monitor Lizard

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 age group (χ2 = 5.001, df=2, p = 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) and village of origin (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.

Trypanosome infection rates inGlossina swynnertoniandG. pallidipesin Ikoma, Musoma District, Tanzania

Parasitology ◽  
1973 ◽  
Vol 66 (2) ◽  
pp. 259-267 ◽  
Author(s):  
S. K. Moloo ◽  
R. F. Steiger ◽  
R. Brun
Keyword(s):  
Salivary Gland ◽  
Infection Rate ◽  
Domestic Animals ◽  
Trypanosome Infection ◽  
Infection Rates ◽  
The Mean ◽  
Animal Trypanosomiasis ◽  
Type Infection

In a survey of animal trypanosomiasis in Musoma District, carried out in October and November 1970, 6344G. swynnertoniwere collected from six different localities of the Ikoma-Serengeti area and 623G. pallidipesfrom Ikoma. These were dissected and examined for trypanosome infections. The mean infection rates ofvivax-type inG. swynnertoniandG. pallidipeswere 12.6% and 7.5%, respectively. Thecongolensegroup infection rates were 2.0% inG. swynnertoniand 1.8% inG. pallidipes. No salivary gland infection was encountered. The incidence of vivax- and congolense-type infections in general increased with age of both the tsetse species, suggesting that the latter can become infected with these trypanosome types at all ages. The infection rate among female tsetse was higher than among males in the six wing-fray categories. This was due to the slower rate of fraying of the wings with age of the former, so that at each wing-fray category the females were generally older than the males.Vivax-type greatly exceededcongolense-type infection rate in bothG. swynnertoniandG. pallidipes. It is suggested that this probably reflects the known greater infectivity of the former group of trypanosomes toGlossina. It is concluded that in Ikoma, where game functions as the reservoir of animal trypanosomiasis and where infected tsetse are abundant, the domestic animals are exposed to a continuous trypanosome challenge.

Trypanosome infection rates inGlossina morsitans submorsitansNewst. in Northern Nigeria

1964 ◽  
Vol 55 (2) ◽  
pp. 219-231 ◽  
Author(s):  
A. M. Jordan
Keyword(s):  
Infection Rate ◽  
Dry Season ◽  
Tsetse Fly ◽  
Effect Of Temperature ◽  
General Effect ◽  
Northern Nigeria ◽  
Trypanosome Infection ◽  
Infection Rates ◽  
Wet Season ◽  
Significant Difference

Previous records and new data on trypanosome infection rates inGlossina morsitans submorsitansNewst. in Northern Nigeria are presented, and discussed in relation to the hosts fed on by this tsetse fly. The new observations were carried out in three areas: at Mando and Gamagira, both lying in a fly-belt north of Kaduna, and in the Yankari Game Reserve in Bauchi Province.Infection rates were obtained by dissection of flies, and the trypanosomes were identified by their locus; the validity of this method of identification is discussed. All infections withTrypanosomaspp. were attributable either to thevivaxgroup or to theconrgolensegroup; nobrucen-group trypanosomes were identified. More than 260 flies from each area were examined during March 1962, at the end of the dry season, and similar numbers during October 1962, at the end of the wet season.There was no significant difference between dry-season and wet-season infection rates in any area. Taking the two seasons together, the rate at Yankari (12%) was significantly higher than the rates at Mando (5%) and Gamagira (3%), which did not differ significantly. These contrasting infection rates could be related to the host species principally fed on by flies in the different areas as shown by blood-meal determinations. The lowest infection rates occurred where Suidae furnished a high proportion of meals (Mando, 51%; Gamagira, 67%) and Bovidae a small proportion (Mando, 16%; Gamagira, 9%). The high infection rate at Yankari was associated with a high proportion of Bovid meals (53%), especially from buffalo (Syncerus nanus) and bushbuck (Tragelaphus scriptus), and a lower proportion of Suid meals (33%). For the three areas the relationship between infection rate and percentage of Bovid meals was statistically significant.The species groups of infecting trypanosomes showed further contrasts between the three areas which were unrelated to the total infection rates. At Gamagira, 81 per cent, of infections werecongolensegroup, and this proportion was significantly higher than that at Mando (45%) or Yankari (37%). The differences could be related to the types of host from which blood-meals were principally derived. The highest proportion ofcongolense-group infections occurred where the highest percentage of meals came from Suidae (Gamagira, 67%), and lower proportions occurred at Mando and Yankari where Suid feeds were relatively fewer (51% and 33%, respectively).These findings are discussed in the light of existing evidence on the factors governing infection rates inGlossina. It is concluded that, within the over-riding influence exerted by temperature through geographical latitude, infection rates are determined by the type of host that forms the principal source of food. In some populations of Glossina the influence of the nature of the main food source can be sufficient to obscure the general effect of temperature in determining the level of infection. Some of the reasons for these relationships are discussed.

scholarly journals Rapid and Accurate Identification of Candida albicans and Candida dubliniensis by Real-Time PCR and Melting Curve Analysis

2018 ◽  
Vol 27 (6) ◽  
pp. 543-548 ◽  
Author(s):  
Mohammad Asadzadeh ◽  
Suhail Ahmad ◽  
Noura Al-Sweih ◽  
Ziauddin Khan
Keyword(s):  
Real Time ◽  
Real Time Pcr ◽  
Gel Electrophoresis ◽  
Melting Curve ◽  
Melting Curve Analysis ◽  
Agarose Gel ◽  
Agarose Gel Electrophoresis ◽  
Pcr Assay ◽  
Candida Spp ◽  
Accurate Identification

Objective: Candida albicans and Candida dubliniensis are germ tube-positive pathogenic yeast species. Accurate identification of these two species is warranted since C. albicans is a highly pathogenic species while C. dubliniensis exhibits increased adherence to buccal epithelial cells, reduced susceptibility to azoles and resistance to flucytosine. We have developed a duplex real-time PCR assay for rapid detection and differentiation between clinical C. albicans and C. dubliniensis isolates. Materials and Methods: A duplex real-time PCR assay was developed by using two species-specific primer pairs and SYBR Green dye to differentiate C. albicans and C. dubliniensis isolates via melting curve analysis of real-time PCR amplicons. Amplification products were also analyzed by agarose gel electrophoresis to confirm real-time PCR results. Results: Melting temperatures (Tm) for reference strains of C. albicans and C. dubliniensis were 86.55 and 82.75°C, respectively. No amplicon was obtained with DNA from reference strains of 8 other common Candida spp. When real-time PCR was applied on 226 clinical isolates previously identified by the Vitek 2 system and/or PCR sequencing of rDNA, Tm values for C. albicans (n = 113) and C. dubliniensis (n = 98) were 86.68 ± 0.529 and 82.616 ± 0.535°C, respectively. The results were confirmed by agarose gel electrophoresis. No amplicon was obtained from 15 isolates belonging to 9 other Candida spp. Conclusions: The real-time PCR assay described here does not require prior identification of clinical yeast isolates as C. albicans/C. dubliniensis by germ tube formation and accurately reports results within 2 h. Detection of amplicons by agarose gel electrophoresis is also suitable for resource-poor settings devoid of real-time PCR facilities.

Luminography – an Alternative Assay for Detection of von Willebrand Factor Multimers

1988 ◽  
Vol 60 (02) ◽  
pp. 133-136 ◽  
Author(s):  
R Schneppenheim ◽  
H Plendl ◽  
U Budde
Keyword(s):  
Von Willebrand Factor ◽  
Gel Electrophoresis ◽  
Detection Methods ◽  
Agarose Gel ◽  
Agarose Gel Electrophoresis ◽  
Luminescence Assay ◽  
Von Willebrand ◽  
Willebrand Factor

SummaryA luminescence assay was adapted for detection of von Willebrand factor multimers subsequent to SDS-agarose gel electrophoresis and electroblotting onto nitrocellulose. The method is as fast as chromogenic detection methods and appears to be as sensitive as autoradiography without the disadvantages of the latter.

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