Literature DB >> 18260516

Glossina dynamics in and around the sleeping sickness endemic Serengeti ecosystem of northwestern Tanzania.

I I Malele1, S M Kinung'hi, H S Nyingilili, L E Matemba, J K Sahani, T D K Mlengeya, M Wambura, S N Kibona.   

Abstract

We investigated the dynamics of Glossina spp. and their role in the transmission of trypanosomiasis in the sleeping sickness endemic Serengeti ecosystem, northwestern Tanzania. The study investigated Glossina species composition, trap density, trypanosome infection rates, and the diversity of trypanosomes infecting the species. Tsetse were trapped using monopyramidal traps in the mornings between 06:00 to 11:00 and transported to the veterinary laboratory in Serengeti National Park where they were sorted into species and sex, and dissected microscopically to determine trypanosome infection rates. Age estimation of dissected flies was also conducted concurrently. Tsetse samples positive for trypanosomes were subjected to PCR to determine the identity of the detected trypanosomes. Out of 2,519 tsetse trapped, 1,522 (60.42%) were G. swynnertoni, 993 (39.42%) were G. pallidipes, three (0.12%) were G. m. morsitans, and one (0.04%) was G. brevipalpis. The trap density for G. swynnertoni was between 1.40 and 14.17 while that of G. pallidipes was between 0.23 and 9.70. Out of 677 dissected G. swynnertoni, 63 flies (9.3%) were infected, of which 62 (98.4%) were females. A total of 199 G. pallidipes was also dissected but none was infected. There was no significant difference between the apparent densities of G. swynnertoni compared to that of G. pallidipes (t = 1.42, p = 0.18). Molecular characterization of the 63 infected G. swynnertoni midguts showed that 19 (30.2%) were trypanosomes associated with suid animals while nine (14.3%) were trypanosomes associated with bovid animals and five samples (7.9%) had T. brucei s.l genomic DNA. Thirty (47.6%) tsetse samples could not be identified. Subsequent PCR to differentiate between T. b. brucei and T. b. rhodesiense showed that all five samples that contained the T. brucei s.l genomic DNA were positive for the SRA molecular marker indicating that they were T. b. rhodesiense. These results indicate that G. swynnertoni plays a major role in the transmission of trypaniosomiasis in the area and that deliberate and sustainable control measures should be initiated and scaled up.

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Year:  2007        PMID: 18260516     DOI: 10.3376/1081-1710(2007)32[263:gdiaat]2.0.co;2

Source DB:  PubMed          Journal:  J Vector Ecol        ISSN: 1081-1710            Impact factor:   1.671


  10 in total

1.  Prevalence of Trypanosoma sp. in cattle from Tanzania estimated by conventional PCR and loop-mediated isothermal amplification (LAMP).

Authors:  Dusit Laohasinnarong; Oriel M M Thekisoe; Imna Malele; Boniface Namangala; Akihiro Ishii; Yasuyuki Goto; Shin-Ichiro Kawazu; Chihiro Sugimoto; Noboru Inoue
Journal:  Parasitol Res       Date:  2011-07-08       Impact factor: 2.289

Review 2.  Improving Sterile Insect Technique (SIT) for tsetse flies through research on their symbionts and pathogens.

Authors:  Adly M M Abd-Alla; Max Bergoin; Andrew G Parker; Nguya K Maniania; Just M Vlak; Kostas Bourtzis; Drion G Boucias; Serap Aksoy
Journal:  J Invertebr Pathol       Date:  2012-07-24       Impact factor: 2.841

3.  Using molecular data for epidemiological inference: assessing the prevalence of Trypanosoma brucei rhodesiense in tsetse in Serengeti, Tanzania.

Authors:  Harriet K Auty; Kim Picozzi; Imna Malele; Steve J Torr; Sarah Cleaveland; Sue Welburn
Journal:  PLoS Negl Trop Dis       Date:  2012-01-31

4.  Sodalis glossinidius prevalence and trypanosome presence in tsetse from Luambe National Park, Zambia.

Authors:  Jonny W Dennis; Simon M Durkin; Jemima E Horsley Downie; Louise C Hamill; Neil E Anderson; Ewan T MacLeod
Journal:  Parasit Vectors       Date:  2014-08-19       Impact factor: 3.876

5.  A Multi-Host Agent-Based Model for a Zoonotic, Vector-Borne Disease. A Case Study on Trypanosomiasis in Eastern Province, Zambia.

Authors:  Simon Alderton; Ewan T Macleod; Neil E Anderson; Kathrin Schaten; Joanna Kuleszo; Martin Simuunza; Susan C Welburn; Peter M Atkinson
Journal:  PLoS Negl Trop Dis       Date:  2016-12-27

6.  Tsetse blood-meal sources, endosymbionts and trypanosome-associations in the Maasai Mara National Reserve, a wildlife-human-livestock interface.

Authors:  Edward Edmond Makhulu; Jandouwe Villinger; Vincent Owino Adunga; Maamun M Jeneby; Edwin Murungi Kimathi; Enock Mararo; Joseph Wang'ang'a Oundo; Ali Abdulahi Musa; Lillian Wambua
Journal:  PLoS Negl Trop Dis       Date:  2021-01-06

7.  Standardizing visual control devices for tsetse flies: East African species Glossina swynnertoni.

Authors:  Furaha Mramba; Francis Oloo; Mechtilda Byamungu; Thomas Kröber; Andrew McMullin; Steve Mihok; Patrick M Guerin
Journal:  PLoS Negl Trop Dis       Date:  2013-02-28

8.  Spatial distribution of Glossina sp. and Trypanosoma sp. in south-western Ethiopia.

Authors:  Reta Duguma; Senbeta Tasew; Abebe Olani; Delesa Damena; Dereje Alemu; Tesfaye Mulatu; Yoseph Alemayehu; Moti Yohannes; Merga Bekana; Antje Hoppenheit; Emmanuel Abatih; Tibebu Habtewold; Vincent Delespaux; Luc Duchateau
Journal:  Parasit Vectors       Date:  2015-08-19       Impact factor: 3.876

9.  Comparative performance of traps in catching tsetse flies (Diptera: Glossinidae) in Tanzania.

Authors:  Imna I Malele; Johnson O Ouma; Hamisi S Nyingilili; Winston A Kitwika; Deusdedit J Malulu; Henry B Magwisha; Eliningeya J Kweka
Journal:  Onderstepoort J Vet Res       Date:  2016-06-23       Impact factor: 1.792

10.  Standardising visual control devices for Tsetse: East and Central African Savannah species Glossina swynnertoni, Glossina morsitans centralis and Glossina pallidipes.

Authors:  Mechtilda Byamungu; Tusevo Zacarie; Alexis Makumyaviri M'Pondi; Philémon Mansinsa Diabakana; Andrew McMullin; Thomas Kröber; Steve Mihok; Patrick M Guerin
Journal:  PLoS Negl Trop Dis       Date:  2018-09-25
  10 in total

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