Evidence map›Paper›PMID 34530992›Full record

ArticleGene2019

Dynamics of repeat-associated plasticity in the aaap gene family in Anaplasma marginale.

Heather M Fallquist, Jin Tao, Xiaoya Cheng, Sebastian Aguilar Pierlé, Shira L Broschat, Kelly A Brayton

Abstract read
PubMed Publisher
In one paragraph

Article in Gene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Heather M FallquistProgram in Genomics, Department of Veterinary Microbiology & Pathology, Washington State University, Pullman, WA 99164-7040, USA.
Jin TaoSchool of Electrical Engineering and Computer Science, Washington State University, Pullman, WA 99164-2752, USA.
Xiaoya ChengProgram in Genomics, Department of Veterinary Microbiology & Pathology, Washington State University, Pullman, WA 99164-7040, USA.
Sebastian Aguilar PierléProgram in Genomics, Department of Veterinary Microbiology & Pathology, Washington State University, Pullman, WA 99164-7040, USA.
Shira L BroschatProgram in Genomics, Department of Veterinary Microbiology & Pathology, Washington State University, Pullman, WA 99164-7040, USA; School of Electrical Engineering and Computer Science, Washington State University, Pullman, WA 99164-2752, USA; Paul G. Allen School for Global Animal Health, Washington State University, Pullman, WA 99164-7090, USA.
Kelly A BraytonProgram in Genomics, Department of Veterinary Microbiology & Pathology, Washington State University, Pullman, WA 99164-7040, USA; School of Electrical Engineering and Computer Science, Washington State University, Pullman, WA 99164-2752, USA; Paul G. Allen School for Global Animal Health, Washington State University, Pullman, WA 99164-7090, USA. Electronic address: kbrayton@wsu.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anaplasmosis, the most prevalent tick-transmitted disease of cattle, is caused by the rickettsial intracellular parasite Anaplasma marginale. The pathogen replicates within a parasitophorous vacuole formed from the invagination of the erythrocyte membrane. Several strains of A. marginale form "tails" or "appendages" which are attached to, and extend out from, the cytoplasmic side of the parasitophorous vacuole. Genomic analysis of the parasite antigen distributed along the appendage led to the discovery of the aaap (Anaplasma appendage associated protein) gene family located within a highly plastic region in the genome. The aaap gene family consists of aaap and several alps (for aaap-like proteins), depending on the strain. These genes/proteins are characterized by repeat sequences. To investigate locus plasticity, different versions of the locus were cloned from the same strain as well as from different strains, sequenced and aligned to identify changes. Our findings show that repeat sequences both within and between genes facilitated rearrangement events within the locus. Structural variation of the locus in the St. Maries strain was further investigated during infection of different cellular environments, i.e., bovine erythrocytes and tick cells, with a reduction in subpopulations of the aaap locus within the tick as compared to erythrocytes. Interestingly, subpopulations bearing alternative locus structures began to arise again when the pathogen was transferred from the tick environment into a naïve calf. Additionally, the Aaap protein expression profile between blood and tick samples showed a regulatory shift, indicating a host-specific response. Alignment of the protein sequences from different species of Anaplasma reveals six similar repeating motifs that appear to be unique to a few species of Anaplasma. The role the aaap locus may play in the pathogenesis of the bovine host or in tick infection/transmission remains unknown; however, the changes in aaap locus subpopulations, locus structure, and protein expression indicate that these genes have a role in strain diversification.

Indexed as

AlpAppendageGenome plasticityTick-borne pathogen

Identifiers

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.