Evidence map›Paper›PMID 41275102›Full record

ArticleBMC genomics2025

Comparative genomics and transcriptomics of the Spiroplasma glossinidia strain sGff reveal insights into host interaction and trypanosome resistance in Glossina fuscipes fuscipes.

Daniel J Bruzzese, Fabian Gstöttenmayer, Brian L Weiss, Hager Khalil, Robert L Mach, Adly M M Abd-Alla, Serap Aksoy

Abstract readComparative Study
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. bioRxiv : the preprint server for biology · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Daniel J BruzzeseDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, USA. daniel.bruzzese@yale.edu.
Fabian GstöttenmayerDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, USA. fabian.gstoettenmayer@yale.edu.
Brian L WeissDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, USA.
Hager KhalilInsect Pest Control Laboratory, Joint FAO/IAEA Centre of Nuclear Techniques in Food and Agriculture, Vienna, Austria.
Robert L MachInstitute of Chemical, Environmental, and Bioscience Engineering, Vienna University of Technology, Vienna, Austria.
Adly M M Abd-AllaInsect Pest Control Laboratory, Joint FAO/IAEA Centre of Nuclear Techniques in Food and Agriculture, Vienna, Austria.
Serap AksoyDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, USA.

Funding

Spiroplasma effects on Tsetse FliesR21AI163969 · NIAID · YALE UNIVERSITY · PI AKSOY, SERAP, WEISS, BRIAN L · 2021 to 2022
$430k
International Atomic Energy Agency D42017NIAID NIH HHS R21 AI163969NIH HHS R21AI163969
6 · The paper itself

Abstract

Tsetse (Glossina spp.) are vectors of African trypanosomes, the causative agents of Human and African Animal trypanosomiases, diseases that remain significant medical and socioeconomic challenges in sub-Saharan Africa. In addition to trypanosomes, tsetse harbor both obligate and facultative symbiotic bacteria that can influence vector competence and reproductive biology. One such facultative symbiont, Spiroplasma glossinidia, infects several tsetse species within the Palpalis subgroup. In Glossina fuscipes fuscipes (Gff), the Spiroplasma glossinidia strain sGff induces a trypanosome-refractory phenotype and negatively impacts reproductive fitness by reducing female fecundity. However, the mechanisms behind these Spiroplasma-derived phenotypes remain poorly understood. Here, we report successful in vitro cultivation of sGff and present complete genomes from three sources: in vitro cultured sGff and sGff isolated from both laboratory-maintained and wild-caught (Uganda) Gff flies. Comparative genomic analyses revealed a high degree of similarity in gene content and synteny among these sGff samples, confirming that they represent isolates of the same strain. Phylogenomic analyses placed sGff within the Spiroplasma poulsonii clade. We found the sGff genome to be highly dynamic, containing numerous mobile genetic elements. Additionally, in silico annotations indicated that sGff relies on its host for both lipids and carbohydrates and can produce several toxins, all of which could be implicated in the observed trypanosome refractory phenotype. Finally, comparative transcriptomic analysis of sGff from host hemolymph versus in vitro culture provided insights into potential factors relevant to host-symbiont interactions. Our findings provide a foundation for understanding the nutritional dialogue between sGff and its host and identify symbiotic products that may contribute to trypanosome resistance. Furthermore, the establishment of an in vitro culture system for sGff represents a significant resource for future functional studies with potential implications for vector control.

Indexed as

Gene Expression ProfilingGenomicsHost-Pathogen InteractionsSpiroplasmaTranscriptomeTrypanosomaTsetse FliesAnimalsFemaleGenome, BacterialPhylogenySymbiosisGlossina fuscipes fuscipesSpiroplasmaSpiroplasma glossinidiaSymbiosisTsetse

Identifiers

PMID41275102
PMCPMC12752236

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.