Evidence map›Paper›PMID 38855918›Full record

ArticleEnvironmental microbiology reports2024

Limited variation in microbial communities across populations of Macrosteles leafhoppers (Hemiptera: Cicadellidae).

Sandra Åhlén Mulio, Agnieszka Zwolińska, Tomasz Klejdysz, Monika Prus-Frankowska, Anna Michalik, Michał Kolasa, Piotr Łukasik

Abstract read
In one paragraph

Article in Environmental microbiology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Article
  6. The facultative intracellular symbiontFrontiers in microbiology · 2025
    Article
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  8. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Sandra Åhlén MulioInstitute of Environmental Sciences, Faculty of Biology, Jagiellonian University, Kraków, Poland.ORCID 0000-0002-0272-1229
Agnieszka ZwolińskaDepartment of Plant Physiology, Faculty of Biology, Adam Mickiewicz University, Poznan, Poland.ORCID 0000-0003-2681-2915
Tomasz KlejdyszInstitute of Plant Protection - National Research Institute, Research Centre for Registration of Agrochemicals, Poznań, Poland.ORCID 0000-0002-9660-9771
Monika Prus-FrankowskaInstitute of Environmental Sciences, Faculty of Biology, Jagiellonian University, Kraków, Poland.ORCID 0000-0002-6684-2556
Anna MichalikDepartment of Developmental Biology and Morphology of Invertebrates, Institute of Zoology and Biomedical Research, Faculty of Biology, Jagiellonian University, Kraków, Poland.ORCID 0000-0003-2952-9867
Michał KolasaInstitute of Environmental Sciences, Faculty of Biology, Jagiellonian University, Kraków, Poland.ORCID 0000-0003-2143-429X
Piotr ŁukasikInstitute of Environmental Sciences, Faculty of Biology, Jagiellonian University, Kraków, Poland.ORCID 0000-0002-4164-6487

Funding

Human Frontier Science Program RGP 0024/2015Narodowa Agencja Wymiany Akademickiej PPN/PPO/2018/1/00015Narodowe Centrum Nauki 2018/30/E/NZ8/00880Narodowe Centrum Nauki 2021/41/B/NZ8/04526
6 · The paper itself

Abstract

Microbial symbionts play crucial roles in insect biology, yet their diversity, distribution, and temporal dynamics across host populations remain poorly understood. In this study, we investigated the spatio-temporal distribution of bacterial symbionts within the widely distributed and economically significant leafhopper genus Macrosteles, with a focus on Macrosteles laevis. Using host and symbiont marker gene amplicon sequencing, we explored the intricate relationships between these insects and their microbial partners. Our analysis of the cytochrome oxidase subunit I (COI) gene data revealed several intriguing findings. First, there was no strong genetic differentiation across M. laevis populations, suggesting gene flow among them. Second, we observed significant levels of heteroplasmy, indicating the presence of multiple mitochondrial haplotypes within individuals. Third, parasitoid infections were prevalent, highlighting the complex ecological interactions involving leafhoppers. The 16S rRNA data confirmed the universal presence of ancient nutritional endosymbionts-Sulcia and Nasuia-in M. laevis. Additionally, we found a high prevalence of Arsenophonus, another common symbiont. Interestingly, unlike most previously studied species, M. laevis exhibited only occasional cases of infection with known facultative endosymbionts and other bacteria. Notably, there was no significant variation in symbiont prevalence across different populations or among sampling years within the same population. Comparatively, facultative endosymbionts such as Rickettsia, Wolbachia, Cardinium and Lariskella were more common in other Macrosteles species. These findings underscore the importance of considering both host and symbiont dynamics when studying microbial associations. By simultaneously characterizing host and symbiont marker gene amplicons in large insect collections, we gain valuable insights into the intricate interplay between insects and their microbial partners. Understanding these dynamics contributes to our broader comprehension of host-microbe interactions in natural ecosystems.

Indexed as

BacteriaHemipteraMicrobiotaRNA, Ribosomal, 16SSymbiosisAnimalsElectron Transport Complex IVPhylogenyElectron Transport Complex IVRNA, Ribosomal, 16S

Identifiers

PMID38855918
PMCPMC11163331

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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.