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Thematische Bibliographien / Environmental aspects of African trypanosomiasis / Zeitschriftenartikel

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Zeitschriftenartikel zum Thema „Environmental aspects of African trypanosomiasis“

Autor: Grafiati

Veröffentlicht am 4. Juni 2021

Zuletzt aktualisiert am 28. Juli 2025

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1

Moore, Sean, Sourya Shrestha, Kyle W. Tomlinson, and Holly Vuong. "Predicting the effect of climate change on African trypanosomiasis: integrating epidemiology with parasite and vector biology." Journal of The Royal Society Interface 9, no. 70 (2011): 817–30. http://dx.doi.org/10.1098/rsif.2011.0654.

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Climate warming over the next century is expected to have a large impact on the interactions between pathogens and their animal and human hosts. Vector-borne diseases are particularly sensitive to warming because temperature changes can alter vector development rates, shift their geographical distribution and alter transmission dynamics. For this reason, African trypanosomiasis (sleeping sickness), a vector-borne disease of humans and animals, was recently identified as one of the 12 infectious diseases likely to spread owing to climate change. We combine a variety of direct effects of tempera

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2

Tripodi, Karina E. J., Simón M. Menendez Bravo, and Julia A. Cricco. "Role of Heme and Heme-Proteins in Trypanosomatid Essential Metabolic Pathways." Enzyme Research 2011 (April 10, 2011): 1–12. http://dx.doi.org/10.4061/2011/873230.

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Around the world, trypanosomatids are known for being etiological agents of several highly disabling and often fatal diseases like Chagas disease (Trypanosoma cruzi), leishmaniasis (Leishmania spp.), and African trypanosomiasis (Trypanosoma brucei). Throughout their life cycle, they must cope with diverse environmental conditions, and the mechanisms involved in these processes are crucial for their survival. In this review, we describe the role of heme in several essential metabolic pathways of these protozoans. Notwithstanding trypanosomatids lack of the complete heme biosynthetic pathway, we

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3

Kennedy, P. G. E. "Human African trypanosomiasis–neurological aspects." Journal of Neurology 253, no. 4 (2006): 411–16. http://dx.doi.org/10.1007/s00415-006-0093-3.

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4

Baker, J. R. "Trypanosomiasis control and African development." Transactions of the Royal Society of Tropical Medicine and Hygiene 81, no. 1 (1987): 84. http://dx.doi.org/10.1016/0035-9203(87)90292-6.

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5

Rice, Henry, Larry Ruben, Simon Gould, A. R. Njogu, and Curtis L. Patton. "Phenothiazines in murine African trypanosomiasis." Transactions of the Royal Society of Tropical Medicine and Hygiene 81, no. 6 (1987): 932. http://dx.doi.org/10.1016/0035-9203(87)90357-9.

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6

Baral, Toya Nath. "Immunobiology of African Trypanosomes: Need of Alternative Interventions." Journal of Biomedicine and Biotechnology 2010 (2010): 1–24. http://dx.doi.org/10.1155/2010/389153.

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Trypanosomiasis is one of the major parasitic diseases for which control is still far from reality. The vaccination approaches by using dominant surface proteins have not been successful, mainly due to antigenic variation of the parasite surface coat. On the other hand, the chemotherapeutic drugs in current use for the treatment of this disease are toxic and problems of resistance are increasing (see Kennedy (2004) and Legros et al. (2002)). Therefore, alternative approaches in both treatment and vaccination against trypanosomiasis are needed at this time. To be able to design and develop such

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7

Gibson, Wendy. "Report on African Trypanosomiasis (Sleeping Sickness)." Transactions of the Royal Society of Tropical Medicine and Hygiene 98, no. 6 (2004): 392. http://dx.doi.org/10.1016/j.trstmh.2004.02.001.

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8

Baker, J. R. "Control and surveillance of African trypanosomiasis." Transactions of the Royal Society of Tropical Medicine and Hygiene 93, no. 3 (1999): 323. http://dx.doi.org/10.1016/s0035-9203(99)90038-x.

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9

Blum, Johannes, Caecilia Schmid, and Christian Burri. "Clinical aspects of 2541 patients with second stage human African trypanosomiasis." Acta Tropica 97, no. 1 (2006): 55–64. http://dx.doi.org/10.1016/j.actatropica.2005.08.001.

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10

Carrington, Mark. "Slippery customers: How African trypanosomes evade mammalian defences." Biochemist 31, no. 4 (2009): 8–11. http://dx.doi.org/10.1042/bio03104008.

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African trypanosomes are excellent parasites and can maintain an infection of a large mammalian host for months or years. In endemic areas, Human African Trypanosomiasis, also called sleeping sickness, has been largely unaffected by the advent of modern medicine, and trypanosomiasis of domestic livestock is a major restraint on productivity in endemic areas and is arguably the major contributor to the institutionalized poverty in much of rural sub-Saharan Africa1,2. A simple way of visualizing the effect of the livestock disease is to compare maps showing the distribution of livestock (www.ilr

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11

Baker, John. "Progress in human African Trypanosomiasis, sleeping sickness." Transactions of the Royal Society of Tropical Medicine and Hygiene 94, no. 1 (2000): 82. http://dx.doi.org/10.1016/s0035-9203(00)90449-8.

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12

Wamwiri, Florence Njeri, and Robert Emojong Changasi. "Tsetse Flies (Glossina) as Vectors of Human African Trypanosomiasis: A Review." BioMed Research International 2016 (2016): 1–8. http://dx.doi.org/10.1155/2016/6201350.

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Human African Trypanosomiasis (HAT) transmitted by the tsetse fly continues to be a public health issue, despite more than a century of research. There are two types of the disease, the chronicgambienseand the acuterhodesiense-HAT. Fly abundance and distribution have been affected by changes in land-use patterns and climate. However, disease transmission still continues. Here, we review some aspects of HAT ecoepidemiology in the context of altered infestation patterns and maintenance of the transmission cycle as well as emerging options in disease and vector control.

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13

Lopes, Rosane Lima, Suzete Araujo Oliveira Gomes, and Carolina Nascimento Spiegel. "An overview of studies on sex pheromones of insect vectors of pathogenic trypanosomatids of medical and veterinary importance." Research, Society and Development 11, no. 11 (2022): e13111132864. http://dx.doi.org/10.33448/rsd-v11i11.32864.

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Insect vectors of Leishmaniases, Chagas disease and African trypanosomiasis remain human health, veterinary and economic problems worldwide. Several sex pheromones molecules that contribute to mating behavior have been identified in these vectors. These chemical signals are potential alternatives to traditional chemical insecticides. This review discusses the diversity of sex pheromone molecules and their role in the mating behavior of insect vectors of Leishmaniases, Chagas disease and African trypanosomiasis. The selection of studies was made based on research and review articles that presen

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14

Giordani, Federica, Manoj Munde, W. David Wilson, et al. "Green Fluorescent Diamidines as Diagnostic Probes for Trypanosomes." Antimicrobial Agents and Chemotherapy 58, no. 3 (2013): 1793–96. http://dx.doi.org/10.1128/aac.02024-13.

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ABSTRACTLight-emitting diode (LED) fluorescence microscopy offers potential benefits in the diagnosis of human African trypanosomiasis and in other aspects of diseases management, such as detection of drug-resistant strains. To advance such approaches, reliable and specific fluorescent markers to stain parasites in human fluids are needed. Here we describe a series of novel green fluorescent diamidines and their suitability as probes with which to stain trypanosomes.

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15

Mejiozem, Brice Olivier Bogning, Gaspard Tékpa, Synthia Ningatoloum Nazita, et al. "Epidemiological, Clinical and Evolutionary Aspects of Human African Trypanosomiasis in Children in Nola." Open Journal of Pediatrics 14, no. 02 (2024): 344–58. http://dx.doi.org/10.4236/ojped.2024.142034.

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16

Chappuis, François, Louis Loutan, Pere Simarro, Veerle Lejon, and Philippe Büscher. "Options for Field Diagnosis of Human African Trypanosomiasis." Clinical Microbiology Reviews 18, no. 1 (2005): 133–46. http://dx.doi.org/10.1128/cmr.18.1.133-146.2005.

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SUMMARY Human African trypanosomiasis (HAT) due to Trypanosoma brucei gambiense or T. b. rhodesiense remains highly prevalent in several rural areas of sub-Saharan Africa and is lethal if left untreated. Therefore, accurate tools are absolutely required for field diagnosis. For T. b. gambiense HAT, highly sensitive tests are available for serological screening but the sensitivity of parasitological confirmatory tests remains insufficient and needs to be improved. Screening for T. b. rhodesiense infection still relies on clinical features in the absence of serological tests available for field

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17

Squarre, David, Ilunga Kabongo, Musso Munyeme, et al. "Human African Trypanosomiasis in the Kafue National Park, Zambia." PLOS Neglected Tropical Diseases 10, no. 5 (2016): e0004567. http://dx.doi.org/10.1371/journal.pntd.0004567.

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18

Schofield, C. J. "Historical aspects of American trypanosomiasis (Chagas' disease)." Transactions of the Royal Society of Tropical Medicine and Hygiene 91, no. 6 (1997): 734–35. http://dx.doi.org/10.1016/s0035-9203(97)90559-9.

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19

Courtin, David, Vincent Jamonneau, Jean-Francois Mathieu, et al. "Comparison of cytokine plasma levels in human African trypanosomiasis." Tropical Medicine and International Health 11, no. 5 (2006): 647–53. http://dx.doi.org/10.1111/j.1365-3156.2006.01612.x.

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20

Truc, P., P. Grébaut, A. Lando, et al. "Epidemiological aspects of the transmission of the parasites causing human African trypanosomiasis in Angola." Annals of Tropical Medicine & Parasitology 105, no. 3 (2011): 261–65. http://dx.doi.org/10.1179/136485911x12987676649467.

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21

Mudji, Junior, Esther Künzli, David Molyneux, and Johannes Blum. "Long-term sequelae of congenital gambiense human African trypanosomiasis." Transactions of The Royal Society of Tropical Medicine and Hygiene 115, no. 8 (2021): 932–36. http://dx.doi.org/10.1093/trstmh/trab082.

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Abstract Background The clinical presentation of gambiense human African trypanosomias (gHAT) is generally considered to be the same among children and adults. In general, when describing the clinical presentation of children with gHAT, no differentiation is made between congenital gHAT and gHAT acquired later. There is a lack of knowledge regarding the signs and symptoms attributable to congenital gHAT and its long-term sequelae. Methods Following an evaluation of the hospital register for gHAT, the authors observed that six children born to mothers with gHAT during their pregnancies still ha

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22

Gibson, Wendy. "Epidemiology and diagnosis of African trypanosomiasis using DNA probes." Transactions of the Royal Society of Tropical Medicine and Hygiene 96 (April 2002): S141—S143. http://dx.doi.org/10.1016/s0035-9203(02)90066-0.

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23

Huet, G., J. L. Lemesre, G. Grard, et al. "Serum lipid and lipoprotein abnormalities in human African trypanosomiasis." Transactions of the Royal Society of Tropical Medicine and Hygiene 84, no. 6 (1990): 792–94. http://dx.doi.org/10.1016/0035-9203(90)90083-q.

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24

Harries, A. D., and J. J. Wirima. "African trypanosomiasis in a Caucasian associated with anaphylactic shock." Transactions of the Royal Society of Tropical Medicine and Hygiene 82, no. 4 (1988): 578. http://dx.doi.org/10.1016/0035-9203(88)90516-0.

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25

Barrett, Michael P. "The elimination of human African trypanosomiasis is in sight: Report from the third WHO stakeholders meeting on elimination of gambiense human African trypanosomiasis." PLOS Neglected Tropical Diseases 12, no. 12 (2018): e0006925. http://dx.doi.org/10.1371/journal.pntd.0006925.

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26

Das, Aatreyee M., Nakul Chitnis, Christian Burri, et al. "Modelling the impact of fexinidazole use on human African trypanosomiasis (HAT) transmission in the Democratic Republic of the Congo." PLOS Neglected Tropical Diseases 15, no. 11 (2021): e0009992. http://dx.doi.org/10.1371/journal.pntd.0009992.

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Gambiense human African trypanosomiasis is a deadly disease that has been declining in incidence since the start of the Century, primarily due to increased screening, diagnosis and treatment of infected people. The main treatment regimen currently in use requires a lumbar puncture as part of the diagnostic process to determine disease stage and hospital admission for drug administration. Fexinidazole is a new oral treatment for stage 1 and non-severe stage 2 human African trypanosomiasis. The World Health Organization has recently incorporated fexinidazole into its treatment guidelines for hum

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27

Wardrop, Nicola A., Peter M. Atkinson, Peter W. Gething, et al. "Bayesian Geostatistical Analysis and Prediction of Rhodesian Human African Trypanosomiasis." PLoS Neglected Tropical Diseases 4, no. 12 (2010): e914. http://dx.doi.org/10.1371/journal.pntd.0000914.

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28

Checchi, Francesco, François Chappuis, Unni Karunakara, Gerardo Priotto, and Daniel Chandramohan. "Accuracy of Five Algorithms to Diagnose Gambiense Human African Trypanosomiasis." PLoS Neglected Tropical Diseases 5, no. 7 (2011): e1233. http://dx.doi.org/10.1371/journal.pntd.0001233.

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29

Gómez-Junyent, Joan, María Jesús Pinazo, Pedro Castro, et al. "Human African Trypanosomiasis in a Spanish traveler returning from Tanzania." PLOS Neglected Tropical Diseases 11, no. 3 (2017): e0005324. http://dx.doi.org/10.1371/journal.pntd.0005324.

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30

Davis, Christopher N., Kat S. Rock, Erick Mwamba Miaka, and Matt J. Keeling. "Village-scale persistence and elimination of gambiense human African trypanosomiasis." PLOS Neglected Tropical Diseases 13, no. 10 (2019): e0007838. http://dx.doi.org/10.1371/journal.pntd.0007838.

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31

Lamour, Sabrina D., Maria Gomez-Romero, Panagiotis A. Vorkas, et al. "Discovery of Infection Associated Metabolic Markers in Human African Trypanosomiasis." PLOS Neglected Tropical Diseases 9, no. 10 (2015): e0004200. http://dx.doi.org/10.1371/journal.pntd.0004200.

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32

Franco, José R., Giuliano Cecchi, Gerardo Priotto, et al. "Monitoring the elimination of human African trypanosomiasis: Update to 2016." PLOS Neglected Tropical Diseases 12, no. 12 (2018): e0006890. http://dx.doi.org/10.1371/journal.pntd.0006890.

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33

Mumba Ngoyi, D., V. Lejon, F. X. N’Siesi, M. Boelaert, and P. Büscher. "Comparison of operational criteria for treatment outcome ingambiensehuman African trypanosomiasis." Tropical Medicine & International Health 14, no. 4 (2009): 438–44. http://dx.doi.org/10.1111/j.1365-3156.2009.02248.x.

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34

Courtioux, Bertrand, Lynda Pervieux, Gedeao Vatunga, et al. "Increased CXCL-13 levels in human African trypanosomiasis meningo-encephalitis." Tropical Medicine & International Health 14, no. 5 (2009): 529–34. http://dx.doi.org/10.1111/j.1365-3156.2009.02263.x.

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35

Boberg, Mikael, Monica Cal, Marcel Kaiser, Rasmus Jansson-Löfmark, Pascal Mäser, and Michael Ashton. "Enantiospecific antitrypanosomal in vitro activity of eflornithine." PLOS Neglected Tropical Diseases 15, no. 7 (2021): e0009583. http://dx.doi.org/10.1371/journal.pntd.0009583.

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The polyamine synthesis inhibitor eflornithine is a recommended treatment for the neglected tropical disease Gambian human African trypanosomiasis in late stage. This parasitic disease, transmitted by the tsetse fly, is lethal unless treated. Eflornithine is administered by repeated intravenous infusions as a racemic mixture of L-eflornithine and D-eflornithine. The study compared the in vitro antitrypanosomal activity of the two enantiomers with the racemic mixture against three Trypanosoma brucei gambiense strains. Antitrypanosomal in vitro activity at varying drug concentrations was analyse

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Pepin, J., and F. Milord. "African trypanosomiasis and drug-induced encephalopathy: risk factors and pathogenesis." Transactions of the Royal Society of Tropical Medicine and Hygiene 85, no. 2 (1991): 222–24. http://dx.doi.org/10.1016/0035-9203(91)90032-t.

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37

McCann, Peter P., Alan J. Bitonti, Cyrus J. Bacchi, and Allen B. Clarkson. "Use of difluoromethylornithine (DFMO, eflornithine) for late-stage African trypanosomiasis." Transactions of the Royal Society of Tropical Medicine and Hygiene 81, no. 4 (1987): 701. http://dx.doi.org/10.1016/0035-9203(87)90465-2.

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38

Nnko, Happiness Jackson, Paul Simon Gwakisa, Anibariki Ngonyoka, Calvin Sindato, and Anna Bond Estes. "Potential impacts of climate change on geographical distribution of three primary vectors of African Trypanosomiasis in Tanzania’s Maasai Steppe: G. m. morsitans, G. pallidipes and G. swynnertoni." PLOS Neglected Tropical Diseases 15, no. 2 (2021): e0009081. http://dx.doi.org/10.1371/journal.pntd.0009081.

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In the Maasai Steppe, public health and economy are threatened by African Trypanosomiasis, a debilitating and fatal disease to livestock (African Animal Trypanosomiasis -AAT) and humans (Human African Trypanosomiasis—HAT), if not treated. The tsetse fly is the primary vector for both HAT and AAT and climate is an important predictor of their occurrence and the parasites they carry. While understanding tsetse fly distribution is essential for informing vector and disease control strategies, existing distribution maps are old and were based on coarse spatial resolution data, consequently, inaccu

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Wastling, Sally L., Kim Picozzi, Abbas S. L. Kakembo, and Susan C. Welburn. "LAMP for Human African Trypanosomiasis: A Comparative Study of Detection Formats." PLoS Neglected Tropical Diseases 4, no. 11 (2010): e865. http://dx.doi.org/10.1371/journal.pntd.0000865.

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40

Aksoy, Serap, Geoffrey Attardo, Matt Berriman, et al. "Human African Trypanosomiasis Research Gets a Boost: Unraveling the Tsetse Genome." PLoS Neglected Tropical Diseases 8, no. 4 (2014): e2624. http://dx.doi.org/10.1371/journal.pntd.0002624.

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41

Mbala, L., R. Matendo, T. Kinkela, M. Mavangu, and M. Mashako. "Congenital African Trypanosomiasis in a Newborn Child with Current Neurologic Symptomatology." Tropical Doctor 26, no. 4 (1996): 186–87. http://dx.doi.org/10.1177/004947559602600419.

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42

Franco, Jose R., Giuliano Cecchi, Gerardo Priotto, et al. "Human African trypanosomiasis cases diagnosed in non-endemic countries (2011–2020)." PLOS Neglected Tropical Diseases 16, no. 11 (2022): e0010885. http://dx.doi.org/10.1371/journal.pntd.0010885.

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Background Sleeping sickness, or human African trypanosomiasis (HAT), is transmitted by tsetse flies in endemic foci in sub-Saharan Africa. Because of international travel and population movements, cases are also occasionally diagnosed in non-endemic countries. Methodology/Principal findings Antitrypanosomal medicines to treat the disease are available gratis through the World Health Organization (WHO) thanks to a public-private partnership, and exclusive distribution of the majority of them enables WHO to gather information on all exported cases. Data collected by WHO are complemented by case

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Junyent, J. Ma Grau, M. Rozman, M. Corachán, R. Estruch, and A. Urbano-Marquez. "An unusual course of West African trypanosomiasis in a Caucasian man." Transactions of the Royal Society of Tropical Medicine and Hygiene 81, no. 6 (1987): 931–32. http://dx.doi.org/10.1016/0035-9203(87)90356-7.

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44

Mulenga, Gloria M., Boniface Namangala, Kalinga Chilongo, et al. "Challenges in the Diagnostic Performance of Parasitological and Molecular Tests in the Surveillance of African Trypanosomiasis in Eastern Zambia." Tropical Medicine and Infectious Disease 6, no. 2 (2021): 68. http://dx.doi.org/10.3390/tropicalmed6020068.

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African animal trypanosomiasis (AAT) control programs rely on active case detection through the screening of animals reared in disease endemic areas. This study compared the application of the polymerase chain reaction (PCR) and microscopy in the detection of trypanosomes in cattle blood in Mambwe, a rural district in eastern Zambia. Blood samples were collected from 227 cattle and tested for infection with trypanosomes using microscopy and Ribosomal RNA Internal Transcribed Spacers (ITS)-PCR. Microscopy on the buffy coat detected 17 cases, whilst thin and thick smears detected 26 cases and 28

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Mumba, Dieudonne, Elaine Bohorquez, Jane Messina, et al. "Prevalence of Human African Trypanosomiasis in the Democratic Republic of the Congo." PLoS Neglected Tropical Diseases 5, no. 8 (2011): e1246. http://dx.doi.org/10.1371/journal.pntd.0001246.

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46

Palmer, Jennifer J., Elizeous I. Surur, Garang W. Goch, et al. "Syndromic Algorithms for Detection of Gambiense Human African Trypanosomiasis in South Sudan." PLoS Neglected Tropical Diseases 7, no. 1 (2013): e2003. http://dx.doi.org/10.1371/journal.pntd.0002003.

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47

Priotto, Gerardo, François Chappuis, Mathieu Bastard, Laurence Flevaud, and Jean-François Etard. "Early Prediction of Treatment Efficacy in Second-Stage Gambiense Human African Trypanosomiasis." PLoS Neglected Tropical Diseases 6, no. 6 (2012): e1662. http://dx.doi.org/10.1371/journal.pntd.0001662.

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48

Kaboré, Justin Windingoudi, Hamidou Ilboudo, Harry Noyes, et al. "Candidate gene polymorphisms study between human African trypanosomiasis clinical phenotypes in Guinea." PLOS Neglected Tropical Diseases 11, no. 8 (2017): e0005833. http://dx.doi.org/10.1371/journal.pntd.0005833.

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49

Holmes, Peter. "First WHO Meeting of Stakeholders on Elimination of Gambiense Human African Trypanosomiasis." PLoS Neglected Tropical Diseases 8, no. 10 (2014): e3244. http://dx.doi.org/10.1371/journal.pntd.0003244.

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50

Hasker, Epco, Jean Kwete, Raquel Inocencio da Luz, et al. "Innovative digital technologies for quality assurance of diagnosis of human African trypanosomiasis." PLOS Neglected Tropical Diseases 12, no. 9 (2018): e0006664. http://dx.doi.org/10.1371/journal.pntd.0006664.

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