Evidence map›Paper›PMID 34078265›Full record

ArticleBMC ecology and evolution2021

The reduced genome of a heritable symbiont from an ectoparasitic feather feeding louse.

Leila Alickovic, Kevin P Johnson, Bret M Boyd

Open access · goldAbstract read
In one paragraph

Article in BMC ecology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.5field-weighted citation impact, top 12% of its field
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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Independent and repeated acquisition ofRoyal Society open science · 2025
    Article
  3. An obligate symbiont ofApplied and environmental microbiology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
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

3 authors at 2 institutions in 1 country.

Leila AlickovicCenter for the Study of Biological Complexity, Virginia Commonwealth University, 1000 W. Cary St., Suite 111, Richmond, VA, 23284-2030, USA.
Kevin P JohnsonIllinois Natural History Survey, Prairie Research Institute, University of Illinois, Champaign, IL, USA.
Bret M BoydCenter for the Study of Biological Complexity, Virginia Commonwealth University, 1000 W. Cary St., Suite 111, Richmond, VA, 23284-2030, USA. boydbm@vcu.edu.
Virginia Commonwealth University · USUniversity of Illinois Urbana-Champaign · US

Funding

CELLULAR MECHANISMS OF CIRCADIAN PACEMAKER AGINGR01AG013426 · NIA · UNIVERSITY OF KENTUCKY · PI MCMAHON, DOUGLAS G · 1996 to 2000
$171k
2001 Gordon Conference on Cell DeathR13AG019269 · NIA · GORDON RESEARCH CONFERENCES · PI VAUX, DAVID L · 2001 to 2001
$10k
AGING AND ENERGY EXPENDITURE AMONG HISPANIC WOMENR03AG012397 · NIA · ST. LUKE'S ROOSEVELT HOSP CTR (NEW YORK) · PI NUNEZ, CHRISTOPHER · 1994 to 1994
–
Virginia Commonwealth University Life Sciences and National Science Foundation awards DEB-1239788Virginia Commonwealth University Life Sciences and National Science Foundation awards DEB-1342604Virginia Commonwealth University Life Sciences and National Science Foundation awards DEB-1855812Virginia Commonwealth University Life Sciences and National Science Foundation awards DEB-1926919
6 · The paper itself

Abstract

backgroundFeather feeding lice are abundant and diverse ectoparasites that complete their entire life cycle on an avian host. The principal or sole source of nutrition for these lice is feathers. Feathers appear to lack four amino acids that the lice would require to complete development and reproduce. Several insect groups have acquired heritable and intracellular bacteria that can synthesize metabolites absent in an insect's diet, allowing insects to feed exclusively on nutrient-poor resources. Multiple species of feather feeding lice have been shown to harbor heritable and intracellular bacteria. We expected that these bacteria augment the louse's diet with amino acids and facilitated the evolution of these diverse and specialized parasites. Heritable symbionts of insects often have small genomes that contain a minimal set of genes needed to maintain essential cell functions and synthesize metabolites absent in the host insect's diet. Therefore, we expected the genome of a bacterial endosymbiont in feather lice would be small, but encode pathways for biosynthesis of amino acids.

resultsWe sequenced the genome of a bacterial symbiont from a feather feeding louse (Columbicola wolffhuegeli) that parasitizes the Pied Imperial Pigeon (Ducula bicolor) and used its genome to predict metabolism of amino acids based on the presence or absence of genes. We found that this bacterial symbiont has a small genome, similar to the genomes of heritable symbionts described in other insect groups. However, we failed to identify many of the genes that we expected would support metabolism of amino acids in the symbiont genome. We also evaluated other gene pathways and features of the highly reduced genome of this symbiotic bacterium.

conclusionsBased on the data collected in this study, it does not appear that this bacterial symbiont can synthesize amino acids needed to complement the diet of a feather feeding louse. Our results raise additional questions about the biology of feather chewing lice and the roles of symbiotic bacteria in evolution of diverse avian parasites.

Indexed as

IschnoceraParasitesAnimalsBacteriaGenome, BacterialSymbiosisEndosymbiontGenome reductionKeratinMetabolic complementationPhthiraptera

Identifiers

PMID34078265
PMCPMC8173840
OpenAlexW3165640234

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.