Evidence map›Paper›PMID 40251883›Full record

ArticleMolecular ecology2025

Evidence for a Role of Extraintestinal Pathogenic Escherichia coli, Enterococcus faecalis and Streptococcus gallolyticus in the Aetiology of Exudative Cloacitis in the Critically Endangered Kākāpō (Strigops habroptilus).

Rebecca K French, Stephanie J Waller, Janelle R Wierenga, Rebecca M Grimwood, James Hodgkinson-Bean, Andrew Digby, Lydia Uddstrom, Daryl Eason, Kākāpō Recovery Team, Lisa S Argilla and 4 more

Abstract read
In one paragraph

Article in Molecular ecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

14 authors.

Rebecca K FrenchDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.ORCID https://orcid.org/0000-0002-5452-6994
Stephanie J WallerDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.ORCID https://orcid.org/0000-0003-0618-9556
Janelle R WierengaDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.ORCID https://orcid.org/0000-0002-4474-9289
Rebecca M GrimwoodDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.ORCID https://orcid.org/0000-0002-7529-9823
James Hodgkinson-BeanDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.ORCID https://orcid.org/0000-0001-9583-8794
Andrew DigbyKākāpō Recovery Programme, Department of Conservation/Te Papa Atawhai, Invercargill, New Zealand.ORCID https://orcid.org/0000-0002-1870-8811
Lydia UddstromKākāpō Recovery Programme, Department of Conservation/Te Papa Atawhai, Invercargill, New Zealand.
Daryl EasonKākāpō Recovery Programme, Department of Conservation/Te Papa Atawhai, Invercargill, New Zealand.
Kākāpō Recovery TeamKākāpō Recovery Programme, Department of Conservation/Te Papa Atawhai, Invercargill, New Zealand.
Lisa S ArgillaDunedin Wildlife Hospital, Otago Polytechnic School of Animal Health, Dunedin, New Zealand.ORCID https://orcid.org/0000-0002-2614-5000
Patrick J BiggsmEpiLab, School of Veterinary Sciences, Massey University, Palmerston North, New Zealand.ORCID https://orcid.org/0000-0002-0285-4101
Adrian CooksonmEpiLab, School of Veterinary Sciences, Massey University, Palmerston North, New Zealand.ORCID https://orcid.org/0000-0002-8197-3386
Nigel P FrenchTāwharau Ora, School of Veterinary Science, Massey University, Palmerston North, New Zealand.ORCID https://orcid.org/0000-0002-6334-0657
Jemma L GeogheganDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.ORCID https://orcid.org/0000-0003-0970-0153

Funding

Royal Society Te Apārangi RDF-20-UOO-007
6 · The paper itself

Abstract

The kākāpō is a critically endangered flightless parrot which suffers from exudative cloacitis, a debilitating disease resulting in inflammation of the vent margin or cloaca. Despite this disease emerging over 20 years ago, the cause of exudative cloacitis remains elusive. We used total RNA sequencing and metatranscriptomic analysis to characterise the infectome of lesions and cloacal swabs from nine kākāpō affected with exudative cloacitis, and compared this to cloacal swabs from 45 non-diseased kākāpō. We identified three bacterial species-Streptococcus gallolyticus, Enterococcus faecalis and Escherichia coli-as significantly more abundant in diseased kākāpō compared to healthy individuals. The genetic diversity observed in both S. gallolyticus and E. faecalis among diseased kākāpō suggests that these bacteria originate from exogenous sources rather than from kākāpō-to-kākāpō transmission. The presence of extraintestinal pathogenic E. coli (ExPEC)-associated virulence factors in the diseased kākāpō population suggests that E. coli may play a critical role in disease progression by facilitating iron acquisition and causing DNA damage in host cells, possibly in association with E. faecalis. No avian viral, fungal nor other parasitic species were identified. These results, combined with the consistent presence of one E. coli gnd sequence type across multiple diseased birds, suggest that this species may be the primary cause of exudative cloacitis. These findings shed light on possible causative agents of exudative cloacitis, and offer insights into the interplay of microbial factors influencing the disease.

Indexed as

Bird DiseasesEnterococcus faecalisEscherichia coliParrotsStreptococcus gallolyticusAnimalsCloacainfectomekakapometatranscriptomicspathogen discoverytotal RNA sequencingwildlife disease

Identifiers

PMID40251883
PMCPMC12717991

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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.