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Citation: Murilla GA, Ndung'u K, Thuita JK, Gitonga PK, Kahiga DT, Auma JE, et al. (2014) Kenya Trypanosomiasis Research Institute Cryobank for Human and Animal Trypanosome Isolates to Support Research: Opportunities and Challenges. PLoS Negl Trop Dis 8(5): e2747. https://doi.org/10.1371/journal.pntd.0002747
Editor: Christian Tschudi, Yale School of Public Health, United States of America
Published: May 22, 2014
Copyright: © 2014 Murilla et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The cryobank was established in 1977 and is maintained by the Kenya Government. Between 2005 and 2006, KARI-TRC received equipment from WHO/TDR as part of upgrading of the bank to be able to collect, preserve, and store more isolates from trypanosomiasis endemic countries. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript
Competing interests: The authours declare that no competing interest exist.
Introduction
Human African trypanosomiasis (HAT) is classified in the category of the most neglected tropical diseases. In man, the disease is caused by two tsetse (Glossina spp.)-transmitted trypanosome subspecies: Trypanosoma brucei gambiense, which is responsible for the chronic form of HAT in West and Central Africa, and T. b. rhodesiense, which causes acute disease in eastern and southern Africa. African animal trypanosomiasis (AAT) is caused by various trypanosome species, the major ones being T. vivax, T. congolense, and T. evansi [1]. Current diagnostic tools are inadequate and diagnosis is complicated, whereas the drugs for treatment are highly toxic and not very effective; patients die if untreated [2]. In 2005, an annual prevalence of 50,000–70,000 cases per year and incidence rates of 15,000–17,000 cases per year were reported [3]. Although recent data from the World Health Organization (WHO) shows that the number of reported cases of HAT declined to less than 10,000 in 2009, leading to speculation that the disease could be eliminated [4], [5], there is great need to maintain vigilance.
The East African Trypanosomiasis Research Organization (EATRO) was established to carry out research and develop technologies for effective control of trypanosomiasis. In view of this, a trypanosome cryobank was established in Tororo, Uganda, in the mid-1950s to provide materials for research. At that time, dry ice was used as a refrigerant, but in 1977 it was replaced with liquid nitrogen. Following the collapse of the East African Community in 1977, the Kenya Trypanosomiasis Research Institute (KETRI) was established to take over the functions of tsetse and trypanosomiasis research in Kenya. The cryobank was therefore transferred to KETRI during this period. In 2003, following a reorganization of research institutions by the Government of Kenya, KETRI was merged with the Kenya Agricultural Research Institute (KARI) and renamed the Trypanosomiasis Research Centre (KARI-TRC). KARI-TRC continued with all the research programmes and activities that were being carried out under KETRI, including collection and preservation of trypanosome stabilates. The institution developed a policy on stabilate collection by scientists and clinicians for cryopreservation. We describe the establishment of the cryobank and procedures used in cryopreservation of stabilates and summarize the data (numbers and types) on trypanosome species stored in the cryobank, which are available for use in research by the scientific community.
The cryobank contains 2,347 stabilates, including 1,747 primary isolates, out of which there are 42 mixed infections and one miscellaneous Herpetomonas muscorum, and 600 derivatives, including six mixed infections. Primary isolates were collected mainly from countries in the eastern Africa region, including Kenya, Uganda, Tanzania, Sudan, and Ethiopia. However, collections or donations from countries outside the region, including Nigeria, Mozambique, Botswana, Germany, and South America, have been added as part of collaborations between KARI-TRC and other institutions around the world. The stabilates were isolated between 1934 and 2010. The majority of the stabilates were recovered between 1960 and 1970 (Figure 1), the same period when some of the worst epidemics occurred, after which the numbers added have been on the decline. The period from 1940 to 1949 coincided with World War II, when the work on trypanosomiasis research and control stalled: the laboratories in eastern Africa that were the source of isolates were closed, only to resume after 1945 when the war came to an end.
Trypanosomes
Trypanosomes are extracellular protozoan parasites which cause disease in humans and animals.
Isolation and cryopreservation of new trypanosome strains from patients in different HAT foci ensures availability of these stabilates for use in parasitological, biochemical, molecular, serological, and pharmacological studies many years after their isolation from the host. Brun et al. [1] observed that one of the major obstacles in the elucidation of the factors responsible for relapses after melarsopol treatment was lack of recent T. b. gambiense isolates from patients from various endemic areas where the problem had been reported. The WHO steering committee on human African trypanosomiasis treatment and the East African Network for Tsetse and Trypanosomiasis (EANETT) have therefore recommended that collection of stabilates be a continuous activity in order to monitor the occurrence and spatial distribution of treatment failure [6]. Since its inception, KETRI has established an institutional policy of encouraging collection of stabilates by scientists and clinicians for cryopreservation. In this paper, we describe the establishment of the cryobank and summarize the data (numbers and types) on trypanosome species stored in the cryobank, which are available for research by the wider scientific community.
Existing data
An electronic database has been developed for the existing data and can be accessed through the KARI website (www.kari.org), which is currently being updated, and the WIPO Re:Search website (www.wipo.int/research/en/partnership/). The data is categorized into human, animal, tsetse fly, derived, and isolates characterized by drug sensitivity and molecular techniques. The total number of stabilates, including localities and period of isolation, is shown in Table 1.
Human infective trypanosomes
Of the 1,745 primary stabilates in the cryobank, 416 (25%) are T. b. rhodesiense, of which 60 were isolated from cerebrospinal spinal fluid (CSF), and 48 (3%) are T. b. gambiense (Table 1). The T. b. gambiense isolates were collected mainly from Uganda and South Sudan. Four hundred and twenty–seven (92%) of the human infective parasites were recovered from patients, four from animals (Table 2), and 33 from tsetse flies (Table 3). The human infective trypanosomes include three which were isolated from one family consisting of a mother, son, and grandson in Lambwe Valley, Kenya.
A small number of the stabilates have been characterized using PCR, procyclic transmission test, and isoenzyme techniques (Table 4) and assessed for drug sensitivity profiles (Table 5). The data shows that only 22% of the cryobank primary isolates have been characterized at the molecular level (Table 4), indicating that there are numerous opportunities for new studies utilizing the uncharacterized stabilates. The infectivity characterization of T. b. gambiense isolates collected from Sudan revealed five isolates which successfully infected Swiss white mice [7].
Also available are trypanosome stabilates isolated from various body fluids, including blood, CSF, peritoneal fluid, and lymph nodes.
Isolates from animals
The cryobank contains 897 trypanosome stabilates that were recovered from different species of animals, including cattle, sheep, goats, camels, pigs, wildlife, rats, and lizards (Table 2). The stabilates consist mainly of T. brucei subsp., T. congolense, and T. vivax. Cattle were the main source of all animal-derived stabilates (71%), whereas camels and wildlife contributed 11.5% and 7%, respectively (Table 2). The wildlife-derived stabilates were isolated from lions, wildebeest, zebra, bushbuck, grey ducker, and impala, among others, before 1974. A total of 18 and 37 stabilates were isolated from goats and sheep, respectively, while a number of miscellaneous species, including T. theileri (2) and T. lewisi (8), were isolated in Uganda between 1966 and 1973. There are 45 stabilates (Table 1) of mixed infections, mainly of T. congolense with T. vivax, T. brucei, or T. simiae. The list also includes species of trypanosomes whose host of isolation was not documented.
Isolates from tsetse flies
The cryobank contains 422 primary trypanosome isolates that were collected from different species of tsetse flies including G. pallidipes, G. brevipalpis, G. morsitans morsitans, G. palpalis palpalis, G. fuscipes fuscipes, G. fuscipleuris, G. swynertoni, G. tachinoides, and G. austeni. Human infective T. b. rhodesiense trypanosomes constituted 8% (33/422) of all tsetse-derived trypanosome stabilates (Table 3).
Derived trypanosome stabilates
These are secondary trypanosomes derived from primary trypanosomes after propagation in either culture or the animal host system. The cryobank has 600 derivatives, of which 26 are cloned stabilates. The clones include 16 T. b. rhodesiense, six T. b. brucei, three T. evansi, and one T. vivax. Derivatives were mainly prepared from T. brucei subsp. and T. congolense.
Isolates characterized using molecular and drug sensitivity techniques
The existing data on the molecular and drug sensitivity patterns of some of the trypanosome stabilates is shown in Tables 4 and 5, respectively. Trypanosomes not characterized by molecular techniques were assigned their species based on their morphology and animal host. These are now undergoing molecular confirmation.
Potential uses
The data contained in the KETRI cryobank, including (1) history of isolates, (2) diversity of localities and of sample sources, (3) size, (4) published and unpublished information on the stabilates, and (5) availability of T. b. gambiense stabilates susceptible to laboratory Swiss white mice, makes it a unique reference research facility on trypanosomiasis. This collection has potential uses in the development and validation of drugs, vaccines, diagnostics, and interrogation of biological phenomenon such as treatment failures. Studies on the effect of storage on the characteristics of the trypanosomes collected over time has been initiated.
Scientists wishing to collaborate and/or enter into partnership on the use of the biospecimens at the KETRI biobank should contact the Centre directly or through the WIPO Re:Search website (www.wipo.int/research/en/partnership/) for details. This data is published in anticipation that it will attract potential partners and collaborators to invest in this facility and make it self-sustaining. It is anticipated that other institutions working in trypanosomiasis-endemic areas will be encouraged to isolate and cryopreserve parasites during regular surveillance and control of African trypanosomiasis for future research and to avoid loss of vital biological information.
Box 1. Advantages and Improvements of the Cryobank
Advantages
- A large well-preserved stock of over 2,000 trypanosome stabilates of economic importance
- A unique collection of viable species of trypanosomes collected from different hosts and countries over a period of more than 50 years
- A collection of clones developed from different species of trypanosomes and availability of trypanosome isolates of mixed infections
Improvements
- Establishment of new networks and/or strengthen the current collaborations for sustained collection and cryopreservation of human and animal infective trypanosome isolates
- Replacement of the current equipment in order to reduce the liquid nitrogen usage and associated costs
- Review guidelines for access to isolates
Acknowledgments
We wish to thank the Director KARI for permission to publish this work. We are grateful to Drs. Dan Masiga and Zablon Njiru for their supervision during the preparation of the computerized database. Special thanks to Mr. John Walubengo for managing the bank since its transfer from Uganda to Kenya until 1998. Dr. Lawrence Godia is gratefully acknowledged for designing the Ms Access data entry database. Drs. Johnson K. Kinyua, Patrick Irungu, and John Kagira are acknowledged for reading and correcting earlier versions of this manuscript.
References
- 1. Brun R, Schumacher R, Schimid C, Kunz C, Burri C (2001) The phenomenon of treatment failures in Human African Trypanosomiasis. Trop Med Int Health 11: 906–914.
- 2. Hide G (1999) History of sleeping sickness in East Africa. Amer Soc Microbiol 12: 112–125.
- 3. WHO (2006) Human African trypanosomiasis (sleeping sickness): epidemiological update. Wkly Epidemiol Rec 81: 71–80.
- 4.
WHO (2010) African trypanosomiasis (sleeping sickness). Available: http://www.who.int/mediacentre/factsheets/fs259/en/. Accessed 14 February 2014.
- 5. Simarro PP, Cecchi G, Paone M, Franco JR, Ruiz ADJA, et al. (2010) The Atlas of human African trypanosomiasis: a contribution to global mapping of neglected tropical diseases. Int J Health Geogr 9: 57.
- 6. WHO (1998) Control and surveillance of African trypanosomiasis. Report of a WHO Expert Committee. World Health Organ Tech Rep Ser 881: 1–114.
- 7. Maina N, Oberle M, Otieno C, Kunz C, Maeser P, et al. (2007) Isolation and propagation of T.b.gambiense from sleeping sickness patients in S. Sudan. Trans R Soc Trop Med Hyg 101: 540–546.
- 8. Gibson W, Wilson A (1983) Characterization of Trypanosoma evansi from camels in Kenya using Isoenzyme electrophoresis. Resear Vet Sc 34: 114–118.
- 9. Masiga D, Gibson WC (1990) Specific probes for (Trypanozoon) evansi based on Kinetoplast DNA minicircles. Mol Bioche Parasitol 40: 279–284.
- 10. Waitumbi J, Murphy NB (1993) Inter- and intra-species differentiation of trypanosomes by genomic fingerprinting with arbitrary primers. Mol Biochem Parasitol 58: 181–186.
- 11. Legros D, Evans S, Maiso F, Enyaru JCK, Mbulamberi D (1999) Risk factors for treatment failure after melarsoprol for Trypanosoma brucei gambiense trypanosomiasis in Uganda. Trans R Soc Trop Med Hyg 93: 439–442.
- 12. Allsopp B, Newton S (1985) Characterization of Trypanosoma vivax from camels in Kenya using isoenzyme analysis. Inter J Parasitol 15: 265–270.
- 13. Godfrey D, Scott CM, Gibson WC, Mehlitz D, Zillmann U (1987) Enzyme polymorphism and the identity of Trypanosoma brucei gambiense. Parasitol 94: 337–347.
- 14. Gibson W, Gashumba JK (1983) Isoenzyme characterization of some Trypanozoo stocks from a recent trypanosomiasis epidemic in Uganda. Trans R Soc Trop Med Hyg 77: 114–118.
- 15. Gibson W, Backhouse T, Griffiths A (2002) The human serum resistance associated gene is ubiquitous and conserved in Trypanosoma brucei rhodesiense throughout East Africa. Infec Gen Evol 25: 1–8.
- 16. Gibson W, Stevens JR, Mwendia CMT, Makumi JN, Ngotho JM, et al. (2001) Unraveling the phylogenetic relationships of African trypanosomes of suids. Parasitology 122: 625–631.
- 17. Njiru Z, Ndung'u K, Matete G, Ndungu JM, Gibson WC (2004) Detection of Trypanosoma brucei rhodesiense in animals from sleeping sickness foci in East Africa using the serum resistance associated (SRA) gene. Acta Trop 90: 249–254.
- 18. Mukani O, Mukunza WF, Kimani J, Njoka PK, Walubengo J (1993) Evaluation of the in vitro transformation technique to distinguish Trypanosoma evansi from cyclically transmitted Trypanozoon stocks. Trop Med Parasitol 44: 108–110.
- 19. Bacchi C, Nathan HC, Glenn TL, Saric VM, Sayer PD, et al. (1990) Differential Susceptibility to DL-α- Difluoromethylornithine in clinical isolates of Trypanosoma brucei rhodesiense. Ant Agen Chemo 34: 1183–1188.
- 20. Yarlet N, Golberg B, Nathan HC, Garofalo J, Bacchi CJ (1991) Differential Sensitivity of Trypanosoma brucei rhodesiense isolates to invitro lysis by Arsenicals. Exp Parasitol 72: 205–215.
- 21. Kagira J, Maina N (2007) Occurrence of multiple drug resistance in Trypanosoma brucei isolated from sleeping sickness patients. Onderste J Vet Resear 74: 17–22.
- 22.
Mdachi RE, Murilla GA, Ochieng JO, Karanja WM, Kinyosi BW, et al.. (1995) The use of multiple doses of Berenil in treatment of resistant trypanosome infections in a mouse model. Kampala, Uganda: International Scientific Council for Trypanosomiasis Research Control. pp. 184–189.
- 23. Sones K, Njogu AR, Holmes PH (1988) Assessment of sensitivity of Trypanosoma congolense to isometamidium chloride: a comparison of tests using cattle and mice. Acta Trop 45: 153–164.
- 24. Gitatha S (1979) Drug trial in mice on T. evansi-like organisms isolated from camels in Kenya. Internat Scien Counc Trypan Resear Cont 3: 254–256.