Colonization of the tsetse fly midgut with commensal Kosakonia cowanii Zambiae inhibits trypanosome infection establishment

• Published in: PLoS pathogens 2019-02, Vol.15 (2), p.e1007470
• Main Authors: Weiss, Brian L, Maltz, Michele A, Vigneron, Aurélien, Wu, Yineng, Walter, Katharine S, O'Neill, Michelle B, Wang, Jingwen, Aksoy, Serap
• Format: Article
• Language: English
• Subjects: 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
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1007470

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.