Colonization of the tsetse fly midgut with commensal Kosakonia cowanii Zambiae inhibits trypanosome infection establishment
Tsetse flies (Glossina spp.) vector pathogenic trypanosomes (Trypanosoma spp.) in sub-Saharan Africa. These parasites cause human and animal African trypanosomiases, which are debilitating diseases that inflict an enormous socio-economic burden on inhabitants of endemic regions. Current disease cont...
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Published in | PLoS pathogens Vol. 15; no. 2; p. e1007470 |
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Main Authors | , , , , , , , |
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Language | English |
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01.02.2019
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Abstract | Tsetse flies (Glossina spp.) vector pathogenic trypanosomes (Trypanosoma spp.) in sub-Saharan Africa. These parasites cause human and animal African trypanosomiases, which are debilitating diseases that inflict an enormous socio-economic burden on inhabitants of endemic regions. Current disease control strategies rely primarily on treating infected animals and reducing tsetse population densities. However, relevant programs are costly, labor intensive and difficult to sustain. As such, novel strategies aimed at reducing tsetse vector competence require development. Herein we investigated whether Kosakonia cowanii Zambiae (Kco_Z), which confers Anopheles gambiae with resistance to Plasmodium, is able to colonize tsetse and induce a trypanosome refractory phenotype in the fly. Kco_Z established stable infections in tsetse's gut and exhibited no adverse effect on the fly's survival. Flies with established Kco_Z infections in their gut were significantly more refractory to infection with two distinct trypanosome species (T. congolense, 6% infection; T. brucei, 32% infection) than were age-matched flies that did not house the exogenous bacterium (T. congolense, 36% infected; T. brucei, 70% infected). Additionally, 52% of Kco_Z colonized tsetse survived infection with entomopathogenic Serratia marcescens, compared with only 9% of their wild-type counterparts. These parasite and pathogen refractory phenotypes result from the fact that Kco_Z acidifies tsetse's midgut environment, which inhibits trypanosome and Serratia growth and thus infection establishment. Finally, we determined that Kco_Z infection does not impact the fecundity of male or female tsetse, nor the ability of male flies to compete with their wild-type counterparts for mates. We propose that Kco_Z could be used as one component of an integrated strategy aimed at reducing the ability of tsetse to transmit pathogenic trypanosomes. |
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AbstractList | Tsetse flies (
Glossina
spp.) vector pathogenic trypanosomes (
Trypanosoma
spp.) in sub-Saharan Africa. These parasites cause human and animal African trypanosomiases, which are debilitating diseases that inflict an enormous socio-economic burden on inhabitants of endemic regions. Current disease control strategies rely primarily on treating infected animals and reducing tsetse population densities. However, relevant programs are costly, labor intensive and difficult to sustain. As such, novel strategies aimed at reducing tsetse vector competence require development. Herein we investigated whether
Kosakonia cowanii
Zambiae (
Kco_Z
), which confers
Anopheles gambiae
with resistance to
Plasmodium
, is able to colonize tsetse and induce a trypanosome refractory phenotype in the fly.
Kco_Z
established stable infections in tsetse’s gut and exhibited no adverse effect on the fly’s survival. Flies with established
Kco_Z
infections in their gut were significantly more refractory to infection with two distinct trypanosome species (
T
.
congolense
, 6% infection;
T
.
brucei
, 32% infection) than were age-matched flies that did not house the exogenous bacterium (
T
.
congolense
, 36% infected;
T
.
brucei
, 70% infected). Additionally, 52% of
Kco_Z
colonized tsetse survived infection with entomopathogenic
Serratia
marcescens, compared with only 9% of their wild-type counterparts. These parasite and pathogen refractory phenotypes result from the fact that
Kco_Z
acidifies tsetse’s midgut environment, which inhibits trypanosome and
Serratia
growth and thus infection establishment. Finally, we determined that
Kco_Z
infection does not impact the fecundity of male or female tsetse, nor the ability of male flies to compete with their wild-type counterparts for mates. We propose that
Kco_Z
could be used as one component of an integrated strategy aimed at reducing the ability of tsetse to transmit pathogenic trypanosomes.
Tsetse flies transmit pathogenic African trypanosomes, which are the causative agents of socio-economically devastating human and animal African trypanosomiases. These diseases are currently controlled in large part by reducing the population size of tsetse vectors through the use of insecticides, traps and sterile insect technique. However, logistic and monetary hurdles often preclude the prolonged application of procedures necessary to maintain these control programs. Thus, novel strategies, including those aimed at sustainably reducing the ability of tsetse to transmit trypanosomes, are presently under development. Herein we stably colonize tsetse flies with a bacterium (
Kosakonia cowanii
Zambiae,
Kco_Z
) that acidifies their midgut, thus rendering the environment inhospitable to infection with two distinct, epidemiologically important trypanosome strains as well as an entomopathogenic bacteria. In addition to inducing a trypanosome refractory phenotype, colonization of tsetse with
Kco_Z
exerts only a modest fitness cost on the fly. Taken together, these findings suggest that
Kco_Z
could be applied to enhance the effectiveness of currently employed tsetse control programs. Tsetse flies (Glossina spp.) vector pathogenic trypanosomes (Trypanosoma spp.) in sub-Saharan Africa. These parasites cause human and animal African trypanosomiases, which are debilitating diseases that inflict an enormous socio-economic burden on inhabitants of endemic regions. Current disease control strategies rely primarily on treating infected animals and reducing tsetse population densities. However, relevant programs are costly, labor intensive and difficult to sustain. As such, novel strategies aimed at reducing tsetse vector competence require development. Herein we investigated whether Kosakonia cowanii Zambiae (Kco_Z), which confers Anopheles gambiae with resistance to Plasmodium, is able to colonize tsetse and induce a trypanosome refractory phenotype in the fly. Kco_Z established stable infections in tsetse’s gut and exhibited no adverse effect on the fly’s survival. Flies with established Kco_Z infections in their gut were significantly more refractory to infection with two distinct trypanosome species (T. congolense, 6% infection; T. brucei, 32% infection) than were age-matched flies that did not house the exogenous bacterium (T. congolense, 36% infected; T. brucei, 70% infected). Additionally, 52% of Kco_Z colonized tsetse survived infection with entomopathogenic Serratia marcescens, compared with only 9% of their wild-type counterparts. These parasite and pathogen refractory phenotypes result from the fact that Kco_Z acidifies tsetse’s midgut environment, which inhibits trypanosome and Serratia growth and thus infection establishment. Finally, we determined that Kco_Z infection does not impact the fecundity of male or female tsetse, nor the ability of male flies to compete with their wild-type counterparts for mates. We propose that Kco_Z could be used as one component of an integrated strategy aimed at reducing the ability of tsetse to transmit pathogenic trypanosomes. |
Audience | Academic |
Author | Maltz, Michele A Aksoy, Serap O'Neill, Michelle B Wu, Yineng Vigneron, Aurélien Wang, Jingwen Weiss, Brian L Walter, Katharine S |
AuthorAffiliation | Pennsylvania State University, UNITED STATES 2 Southern Connecticut State University, New Haven, Connecticut, United States of America 1 Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America |
AuthorAffiliation_xml | – name: 2 Southern Connecticut State University, New Haven, Connecticut, United States of America – name: 1 Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America – name: Pennsylvania State University, UNITED STATES |
Author_xml | – sequence: 1 givenname: Brian L orcidid: 0000-0003-1576-3556 surname: Weiss fullname: Weiss, Brian L organization: Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America – sequence: 2 givenname: Michele A surname: Maltz fullname: Maltz, Michele A organization: Southern Connecticut State University, New Haven, Connecticut, United States of America – sequence: 3 givenname: Aurélien orcidid: 0000-0003-4986-6465 surname: Vigneron fullname: Vigneron, Aurélien organization: Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America – sequence: 4 givenname: Yineng surname: Wu fullname: Wu, Yineng organization: Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America – sequence: 5 givenname: Katharine S orcidid: 0000-0003-0065-2204 surname: Walter fullname: Walter, Katharine S organization: Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America – sequence: 6 givenname: Michelle B orcidid: 0000-0002-2079-4122 surname: O'Neill fullname: O'Neill, Michelle B organization: Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America – sequence: 7 givenname: Jingwen surname: Wang fullname: Wang, Jingwen organization: Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America – sequence: 8 givenname: Serap orcidid: 0000-0001-9941-143X surname: Aksoy fullname: Aksoy, Serap organization: Yale School of Public Health, Department of Epidemiology of Microbial Diseases, New Haven, Connecticut, United States of America |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30817773$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | COPYRIGHT 2019 Public Library of Science 2019 Weiss et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2019 Weiss et al 2019 Weiss et al |
Copyright_xml | – notice: COPYRIGHT 2019 Public Library of Science – notice: 2019 Weiss et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: 2019 Weiss et al 2019 Weiss et al |
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DocumentTitleAlternate | Commensal Kosakonia inhibits trypanosome infection establishment in tsetse’s midgut |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The authors have declared that no competing interests exist. |
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Snippet | Tsetse flies (Glossina spp.) vector pathogenic trypanosomes (Trypanosoma spp.) in sub-Saharan Africa. These parasites cause human and animal African... Tsetse flies ( Glossina spp.) vector pathogenic trypanosomes ( Trypanosoma spp.) in sub-Saharan Africa. These parasites cause human and animal African... |
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SubjectTerms | Acidification Adult Africa South of the Sahara Analysis Animals Anopheles Anopheles - microbiology Bacteria Bacterial infections Biology and Life Sciences Colonization Commensalism Disease Disease control Enterobacteriaceae Epidemiology Fecundity Female Flies Humans Infections Investigations Male Medicine and Health Sciences Microbiota Midgut Mosquito Vectors - microbiology Mosquito Vectors - parasitology Mosquitoes Novels Parasites Phenotypes Public health Serratia marcescens Software Symbiosis Trends Trypanosoma Trypanosoma brucei brucei - pathogenicity Trypanosoma congolense - pathogenicity Trypanosome Trypanosomiasis, African - metabolism Trypanosomiasis, African - microbiology Trypanosomiasis, African - parasitology Trypanosomiasis, African - prevention & control Tsetse Flies - microbiology Tsetse Flies - parasitology |
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Title | Colonization of the tsetse fly midgut with commensal Kosakonia cowanii Zambiae inhibits trypanosome infection establishment |
URI | https://www.ncbi.nlm.nih.gov/pubmed/30817773 https://www.proquest.com/docview/2251133566 https://search.proquest.com/docview/2187534491 https://pubmed.ncbi.nlm.nih.gov/PMC6394900 https://doaj.org/article/76e43cc865064dd09e6cb410c889bb72 http://dx.doi.org/10.1371/journal.ppat.1007470 |
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