Evidence map›Paper›PMID 16041027›Full record

ArticleInfection and immunity2005

Establishment of cloned Anaplasma phagocytophilum and analysis of p44 gene conversion within an infected horse and infected SCID mice.

Quan Lin, Yasuko Rikihisa

Open access · greenAbstract read
In one paragraph

Article in Infection and immunity, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Generation of Population-Level Diversity inPathogens (Basel, Switzerland) · 2025
    Article
  3. Differential Susceptibility of Male Versus Female Laboratory Mice toTropical medicine and infectious disease · 2018
    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

2 authors at 1 institution in 1 country.

Quan LinDepartment of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, 1925 Coffey Road, Columbus, OH 43210-1093, USA.
Yasuko Rikihisa
The Ohio State University · US

Funding

Comparison of Human Ehrlichiosis Agent GenomesR01AI047885 · NIAID · OHIO STATE UNIVERSITY · PI RIKIHISA, YASUKO · 2000 to 2010
$3.0M
GENE EXPRESSION BY HUMAN GRANULOCYTIC EHRLICHIOSIS AGR01AI047407 · NIAID · OHIO STATE UNIVERSITY · PI RIKIHISA, YASUKO · 2000 to 2004
$1.6M
NIAID NIH HHS AI47407NIAID NIH HHS R01 AI047407NIAID NIH HHS R01 AI047885NIAID NIH HHS R01 AI47885
6 · The paper itself

Abstract

Diverse p44 alleles at the p44 expression locus (p44Es) encoding surface-exposed major membrane proteins, P44s, of Anaplasma phagocytophilum were hypothesized to be garnered by recombination to enact antigenic variation. However, this hypothesis has not been proven so far, due to inability to clone this obligate intragranulocytic rickettsia. To define the p44E recombination, we developed a novel method to clone A. phagocytophilum. This isogenic cloned population containing a defined p44E was used to infect a naive horse and severe combined immunodeficiency (SCID) mice. During a 58-day infection period in the blood of the horse, p44E conversion was evident in a total of 11 new p44Es, 48% (115/242) of the sequenced p44E population. During a 50-day infection period in the blood of SCID mice, p44E conversion was manifested in a total of 13 new p44Es, 42% (192/460) of the p44E population. Thus, similar levels of p44E convertants were detected in either the presence or absence of an acquired immune system, suggesting that T- and B-cell immune pressure was not essential for recombination and/or selection of the p44E variants. Analysis of sequentially changed p44Es revealed that the entire central hypervariable region of donor p44 pseudogenes or of donor full-length p44s replaced the same region of the resident p44E as a cassette. Putative recombination points were detected within p44 conserved regions flanking the central hypervariable region by the TOPALi analysis. Our results unambiguously demonstrated p44E recombination. The cloning method developed would facilitate precise analysis of the recombination process and the extent of diversity which the recombination creates in the antigenic repertoire.

Indexed as

Gene ConversionAnaplasma phagocytophilumAnimalsBacterial Outer Membrane ProteinsBase SequenceCell Culture TechniquesEhrlichiosisHorsesMiceMice, SCIDMolecular Sequence DataBacterial Outer Membrane Proteinsp44 protein, Anaplasma phagocytophila

Identifiers

PMID16041027
PMCPMC1201200
OpenAlexW2137034833

What OpenQuestion holds

Textmetadata
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.