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Successful long-term maintenance of Mansonella perstans in an in vitro culture system

BACKGROUND: Approximately 114 million people are infected with Mansonella perstans in large proportions of Africa. In contrast to other filariae that infect humans, M. perstans-infected individuals show no distinct pathology or specific clinical picture, indicating a well-tuned adaptation to the hos...

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Autores principales: Njouendou, Abdel Jelil, Ritter, Manuel, Ndongmo, Winston Patrick Chounna, Kien, Chi Anizette, Narcisse, Gandjui Tchamatchoua Victor, Fombad, Fanny Fri, Tayong, Dizzle Bita, Pfarr, Kenneth, Layland, Laura E., Hoerauf, Achim, Wanji, Samuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681788/
https://www.ncbi.nlm.nih.gov/pubmed/29126431
http://dx.doi.org/10.1186/s13071-017-2515-8
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author Njouendou, Abdel Jelil
Ritter, Manuel
Ndongmo, Winston Patrick Chounna
Kien, Chi Anizette
Narcisse, Gandjui Tchamatchoua Victor
Fombad, Fanny Fri
Tayong, Dizzle Bita
Pfarr, Kenneth
Layland, Laura E.
Hoerauf, Achim
Wanji, Samuel
author_facet Njouendou, Abdel Jelil
Ritter, Manuel
Ndongmo, Winston Patrick Chounna
Kien, Chi Anizette
Narcisse, Gandjui Tchamatchoua Victor
Fombad, Fanny Fri
Tayong, Dizzle Bita
Pfarr, Kenneth
Layland, Laura E.
Hoerauf, Achim
Wanji, Samuel
author_sort Njouendou, Abdel Jelil
collection PubMed
description BACKGROUND: Approximately 114 million people are infected with Mansonella perstans in large proportions of Africa. In contrast to other filariae that infect humans, M. perstans-infected individuals show no distinct pathology or specific clinical picture, indicating a well-tuned adaptation to the host. In addition, since M. perstans adult worms reside in serous cavities which are difficult to access, research has been hindered and there is a paucity of knowledge about the biology of M. perstans, especially the development of the different life stages as well as M. perstans-driven immune responses. Thus in this study, an in vitro culture system was developed which allows an in-depth analysis of M. perstans. RESULTS: Culicoides species were caught in Ediki (Kumba), Southwest Region within Cameroon following a blood meal on a microfilaremic donor that had 1500 microfilariae/ml of peripheral blood and kept in captivity for 12 days at 23 °C. In a pilot experiment, 15 infective larvae were obtained from the midges and co-cultured with a confluent monolayer of monkey kidney epithelial cells (LLC-MK2) in DMEM medium supplemented with 10% FBS for up to 77 days. The resulting survival rates of 33% revealed that the cell-conditioned medium was suitable for long-term maintenance of M. perstans worms. To confirm these preliminary observations, 249 infective larvae were cultured for 50 days and their development was monitored daily and microscopically graded for motility. In total, 170 (68.3%) filariae survived and 124 (49.8%) larvae moulted between days 21–30 to become L5 stage larvae which were motile and showed continuous vigorous movement. CONCLUSION: We have established an in vitro culture system for the generation and long-term maintenance of viable M. perstans worms. This technique will be an important tool to study parasite biology and development, the role in host immunity, and might be helpful to discover novel treatment strategies against this filariae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-017-2515-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-56817882017-11-17 Successful long-term maintenance of Mansonella perstans in an in vitro culture system Njouendou, Abdel Jelil Ritter, Manuel Ndongmo, Winston Patrick Chounna Kien, Chi Anizette Narcisse, Gandjui Tchamatchoua Victor Fombad, Fanny Fri Tayong, Dizzle Bita Pfarr, Kenneth Layland, Laura E. Hoerauf, Achim Wanji, Samuel Parasit Vectors Short Report BACKGROUND: Approximately 114 million people are infected with Mansonella perstans in large proportions of Africa. In contrast to other filariae that infect humans, M. perstans-infected individuals show no distinct pathology or specific clinical picture, indicating a well-tuned adaptation to the host. In addition, since M. perstans adult worms reside in serous cavities which are difficult to access, research has been hindered and there is a paucity of knowledge about the biology of M. perstans, especially the development of the different life stages as well as M. perstans-driven immune responses. Thus in this study, an in vitro culture system was developed which allows an in-depth analysis of M. perstans. RESULTS: Culicoides species were caught in Ediki (Kumba), Southwest Region within Cameroon following a blood meal on a microfilaremic donor that had 1500 microfilariae/ml of peripheral blood and kept in captivity for 12 days at 23 °C. In a pilot experiment, 15 infective larvae were obtained from the midges and co-cultured with a confluent monolayer of monkey kidney epithelial cells (LLC-MK2) in DMEM medium supplemented with 10% FBS for up to 77 days. The resulting survival rates of 33% revealed that the cell-conditioned medium was suitable for long-term maintenance of M. perstans worms. To confirm these preliminary observations, 249 infective larvae were cultured for 50 days and their development was monitored daily and microscopically graded for motility. In total, 170 (68.3%) filariae survived and 124 (49.8%) larvae moulted between days 21–30 to become L5 stage larvae which were motile and showed continuous vigorous movement. CONCLUSION: We have established an in vitro culture system for the generation and long-term maintenance of viable M. perstans worms. This technique will be an important tool to study parasite biology and development, the role in host immunity, and might be helpful to discover novel treatment strategies against this filariae. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13071-017-2515-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-10 /pmc/articles/PMC5681788/ /pubmed/29126431 http://dx.doi.org/10.1186/s13071-017-2515-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Short Report
Njouendou, Abdel Jelil
Ritter, Manuel
Ndongmo, Winston Patrick Chounna
Kien, Chi Anizette
Narcisse, Gandjui Tchamatchoua Victor
Fombad, Fanny Fri
Tayong, Dizzle Bita
Pfarr, Kenneth
Layland, Laura E.
Hoerauf, Achim
Wanji, Samuel
Successful long-term maintenance of Mansonella perstans in an in vitro culture system
title Successful long-term maintenance of Mansonella perstans in an in vitro culture system
title_full Successful long-term maintenance of Mansonella perstans in an in vitro culture system
title_fullStr Successful long-term maintenance of Mansonella perstans in an in vitro culture system
title_full_unstemmed Successful long-term maintenance of Mansonella perstans in an in vitro culture system
title_short Successful long-term maintenance of Mansonella perstans in an in vitro culture system
title_sort successful long-term maintenance of mansonella perstans in an in vitro culture system
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681788/
https://www.ncbi.nlm.nih.gov/pubmed/29126431
http://dx.doi.org/10.1186/s13071-017-2515-8
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