Evidence map›Paper›PMID 40269010›Full record

ArticleScientific reports2025

Bacterial symbiont as game changers for Aphis craccivora Koch's fitness and survival across distinct climate types.

Minoo Heidari Latibari, Diana Carolina Arias-Penna, Mostafa Ghafouri Moghaddam, Buntika A Butcher

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

4 authors.

Minoo Heidari LatibariIntegrative Insect Ecology Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.ORCID http://orcid.org/0000-0003-4158-8034
Diana Carolina Arias-PennaDepartment of Entomology, University of Illinois, 320 Morrill Hall, 505 S. Goodwin Ave., Urbana, IL, 61801, USA.ORCID http://orcid.org/0000-0002-9601-3038
Mostafa Ghafouri MoghaddamIntegrative Insect Ecology Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand.ORCID http://orcid.org/0000-0002-1942-9689
Buntika A ButcherIntegrative Insect Ecology Research Unit, Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand. buntika.a@chula.ac.th.ORCID http://orcid.org/0000-0002-0541-0709

Funding

Thailand Science Research and Innovation BCG_FF_68_178_2300_039
6 · The paper itself

Abstract

Symbiotic bacteria play a crucial role in the survival, development, and adaptation of aphids to environmental conditions. Buchnera aphidicola (Enterobacterales: Erwiniaceae), the obligate endosymbiont of aphids, is essential for their fitness, while facultative symbionts may provide additional ecological advantages under specific conditions. A comprehensive understanding of how these symbiotic relationships respond to different climatic environments is essential for assessing aphid adaptability and potential implications for biological control. The present study investigates the vital interactions between the obligate bacterial endosymbiont, Buchnera aphidicola, and four facultative bacterial endosymbionts (Arsenophonus sp., Hamiltonella defensa, Serratia symbiotica, and Regiella insecticola), in black cowpea aphid (BCA), in the context of different climate conditions. The BCA specimens were obtained from the leaves of the host plant, alfalfa, cultivated in three distinct climates: cold semi-arid, hot desert, and humid subtropical climates. The findings, as anticipated, indicated a pervasive prevalence of B. aphidicola in BCAs infesting alfalfa crops across all three climate types. In contrast, the BCAs of each climate type exhibited a distinct array of facultative symbionts. The highest number of facultative endosymbionts was exhibited by BCAs from the humid subtropical climate, followed by BCAs from the cold semi-arid climate, whereas none of them were detected in BCAs from the hot desert climate. Rigiella insecticola was not detected molecularly in any of the BCAs from the three climates. Following the eradication of the obligate symbiont Buchnera aphidicola by the antibiotic rifampicin in BCAs, the effects on three categories of parameters were assessed, including life cycle stages, reproductive traits, and external morphological characteristics of adults. The most significant adverse effects were observed in BCAs inhabiting hot desert followed by those inhabiting cold semi-arid climate; detrimental effects in BCAs of the humid subtropical climate were considerably less pronounced. The observed discrepancies in the parameters of BCAs from the humid subtropical climate can be attributed to the presence of a greater number of facultative symbionts, especially the presence of Serratia symbiotica (Enterobacterales: Yersiniaceae). Following the eradication of B. aphidicola, this facultative symbiont continues to complement the functions of B. aphidicola in the host's survival. Conversely, the low presence of facultative symbionts in cold semi-arid climate or even their absence in hot desert climate exacerbates the negative effects of obligate symbiont eradication. These findings highlight the crucial role of symbionts in aphid biology across a spectrum of climatic conditions, and suggest that shifts in symbiotic relationships may modulate aphid fitness, which could have implications for biological control programs.

Indexed as

AphidsSymbiosisAnimalsBuchneraClimateEnterobacteriaceaeMedicago sativaSerratiaAntibioticBlack cowpea aphidClimateObligate and facultative symbiotic bacteria

Identifiers

PMID40269010
PMCPMC12019319

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Registered trials

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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.