Infection with endosymbiotic Spiroplasma disrupts tsetse (Glossina fuscipes fuscipes) metabolic and reproductive homeostasis.

Tsetse flies (Glossina spp.) house a population-dependent assortment of microorganisms that can include pathogenic African trypanosomes and maternally transmitted endosymbiotic bacteria, the latter of which mediate numerous aspects of their host's metabolic, reproductive, and immune physiologie...

Full description

Bibliographic Details
Main Authors: Jae Hak Son, Brian L Weiss, Daniela I Schneider, Kiswend-Sida M Dera, Fabian Gstöttenmayer, Robert Opiro, Richard Echodu, Norah P Saarman, Geoffrey M Attardo, Maria Onyango, Adly M M Abd-Alla, Serap Aksoy
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-09-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1009539
_version_ 1818311072945274880
author Jae Hak Son
Brian L Weiss
Daniela I Schneider
Kiswend-Sida M Dera
Fabian Gstöttenmayer
Robert Opiro
Richard Echodu
Norah P Saarman
Geoffrey M Attardo
Maria Onyango
Adly M M Abd-Alla
Serap Aksoy
author_facet Jae Hak Son
Brian L Weiss
Daniela I Schneider
Kiswend-Sida M Dera
Fabian Gstöttenmayer
Robert Opiro
Richard Echodu
Norah P Saarman
Geoffrey M Attardo
Maria Onyango
Adly M M Abd-Alla
Serap Aksoy
author_sort Jae Hak Son
collection DOAJ
description Tsetse flies (Glossina spp.) house a population-dependent assortment of microorganisms that can include pathogenic African trypanosomes and maternally transmitted endosymbiotic bacteria, the latter of which mediate numerous aspects of their host's metabolic, reproductive, and immune physiologies. One of these endosymbionts, Spiroplasma, was recently discovered to reside within multiple tissues of field captured and laboratory colonized tsetse flies grouped in the Palpalis subgenera. In various arthropods, Spiroplasma induces reproductive abnormalities and pathogen protective phenotypes. In tsetse, Spiroplasma infections also induce a protective phenotype by enhancing the fly's resistance to infection with trypanosomes. However, the potential impact of Spiroplasma on tsetse's viviparous reproductive physiology remains unknown. Herein we employed high-throughput RNA sequencing and laboratory-based functional assays to better characterize the association between Spiroplasma and the metabolic and reproductive physiologies of G. fuscipes fuscipes (Gff), a prominent vector of human disease. Using field-captured Gff, we discovered that Spiroplasma infection induces changes of sex-biased gene expression in reproductive tissues that may be critical for tsetse's reproductive fitness. Using a Gff lab line composed of individuals heterogeneously infected with Spiroplasma, we observed that the bacterium and tsetse host compete for finite nutrients, which negatively impact female fecundity by increasing the length of intrauterine larval development. Additionally, we found that when males are infected with Spiroplasma, the motility of their sperm is compromised following transfer to the female spermatheca. As such, Spiroplasma infections appear to adversely impact male reproductive fitness by decreasing the competitiveness of their sperm. Finally, we determined that the bacterium is maternally transmitted to intrauterine larva at a high frequency, while paternal transmission was also noted in a small number of matings. Taken together, our findings indicate that Spiroplasma exerts a negative impact on tsetse fecundity, an outcome that could be exploited for reducing tsetse population size and thus disease transmission.
first_indexed 2024-12-13T07:56:09Z
format Article
id doaj.art-f411699219a84846aee98d0f354ea7a4
institution Directory Open Access Journal
issn 1553-7366
1553-7374
language English
last_indexed 2024-12-13T07:56:09Z
publishDate 2021-09-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS Pathogens
spelling doaj.art-f411699219a84846aee98d0f354ea7a42022-12-21T23:54:32ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742021-09-01179e100953910.1371/journal.ppat.1009539Infection with endosymbiotic Spiroplasma disrupts tsetse (Glossina fuscipes fuscipes) metabolic and reproductive homeostasis.Jae Hak SonBrian L WeissDaniela I SchneiderKiswend-Sida M DeraFabian GstöttenmayerRobert OpiroRichard EchoduNorah P SaarmanGeoffrey M AttardoMaria OnyangoAdly M M Abd-AllaSerap AksoyTsetse flies (Glossina spp.) house a population-dependent assortment of microorganisms that can include pathogenic African trypanosomes and maternally transmitted endosymbiotic bacteria, the latter of which mediate numerous aspects of their host's metabolic, reproductive, and immune physiologies. One of these endosymbionts, Spiroplasma, was recently discovered to reside within multiple tissues of field captured and laboratory colonized tsetse flies grouped in the Palpalis subgenera. In various arthropods, Spiroplasma induces reproductive abnormalities and pathogen protective phenotypes. In tsetse, Spiroplasma infections also induce a protective phenotype by enhancing the fly's resistance to infection with trypanosomes. However, the potential impact of Spiroplasma on tsetse's viviparous reproductive physiology remains unknown. Herein we employed high-throughput RNA sequencing and laboratory-based functional assays to better characterize the association between Spiroplasma and the metabolic and reproductive physiologies of G. fuscipes fuscipes (Gff), a prominent vector of human disease. Using field-captured Gff, we discovered that Spiroplasma infection induces changes of sex-biased gene expression in reproductive tissues that may be critical for tsetse's reproductive fitness. Using a Gff lab line composed of individuals heterogeneously infected with Spiroplasma, we observed that the bacterium and tsetse host compete for finite nutrients, which negatively impact female fecundity by increasing the length of intrauterine larval development. Additionally, we found that when males are infected with Spiroplasma, the motility of their sperm is compromised following transfer to the female spermatheca. As such, Spiroplasma infections appear to adversely impact male reproductive fitness by decreasing the competitiveness of their sperm. Finally, we determined that the bacterium is maternally transmitted to intrauterine larva at a high frequency, while paternal transmission was also noted in a small number of matings. Taken together, our findings indicate that Spiroplasma exerts a negative impact on tsetse fecundity, an outcome that could be exploited for reducing tsetse population size and thus disease transmission.https://doi.org/10.1371/journal.ppat.1009539
spellingShingle Jae Hak Son
Brian L Weiss
Daniela I Schneider
Kiswend-Sida M Dera
Fabian Gstöttenmayer
Robert Opiro
Richard Echodu
Norah P Saarman
Geoffrey M Attardo
Maria Onyango
Adly M M Abd-Alla
Serap Aksoy
Infection with endosymbiotic Spiroplasma disrupts tsetse (Glossina fuscipes fuscipes) metabolic and reproductive homeostasis.
PLoS Pathogens
title Infection with endosymbiotic Spiroplasma disrupts tsetse (Glossina fuscipes fuscipes) metabolic and reproductive homeostasis.
title_full Infection with endosymbiotic Spiroplasma disrupts tsetse (Glossina fuscipes fuscipes) metabolic and reproductive homeostasis.
title_fullStr Infection with endosymbiotic Spiroplasma disrupts tsetse (Glossina fuscipes fuscipes) metabolic and reproductive homeostasis.
title_full_unstemmed Infection with endosymbiotic Spiroplasma disrupts tsetse (Glossina fuscipes fuscipes) metabolic and reproductive homeostasis.
title_short Infection with endosymbiotic Spiroplasma disrupts tsetse (Glossina fuscipes fuscipes) metabolic and reproductive homeostasis.
title_sort infection with endosymbiotic spiroplasma disrupts tsetse glossina fuscipes fuscipes metabolic and reproductive homeostasis
url https://doi.org/10.1371/journal.ppat.1009539
work_keys_str_mv AT jaehakson infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT brianlweiss infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT danielaischneider infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT kiswendsidamdera infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT fabiangstottenmayer infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT robertopiro infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT richardechodu infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT norahpsaarman infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT geoffreymattardo infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT mariaonyango infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT adlymmabdalla infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis
AT serapaksoy infectionwithendosymbioticspiroplasmadisruptstsetseglossinafuscipesfuscipesmetabolicandreproductivehomeostasis