Evidence map›Paper›PMID 33321227›Full record

ArticleInfection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases2021

Non-B variants of HIV-1 in San Francisco, California.

Kara J O'Keefe, Sharon Pipkin, Robin Fatch, Susan Scheer, Teri Liegler, Willi McFarland, Robert M Grant, Hong-Ha M Truong

Abstract read
In one paragraph

Article in Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases, 2021. 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

8 authors.

Kara J O'KeefeDepartment of Medicine, University of California, San Francisco, CA 94158, USA. Electronic address: kara.okeefe@gmail.com.
Sharon PipkinDepartment of Public Health, San Francisco, CA 94102, USA. Electronic address: sharon.pipkin@sfdph.org.
Robin FatchDepartment of Epidemiology and Biostatistics, University of California, San Francisco 94158, USA. Electronic address: robin.fatch@ucsf.edu.
Susan ScheerDepartment of Public Health, San Francisco, CA 94102, USA. Electronic address: susan.scheer@sfdph.org.
Teri LieglerDepartment of Medicine, University of California, San Francisco, CA 94158, USA.
Willi McFarlandDepartment of Public Health, San Francisco, CA 94102, USA; Department of Epidemiology and Biostatistics, University of California, San Francisco 94158, USA. Electronic address: willi.mcfarland@sfdph.org.
Robert M GrantDepartment of Medicine, University of California, San Francisco, CA 94158, USA. Electronic address: robert.grant@ucsf.edu.
Hong-Ha M TruongDepartment of Medicine, University of California, San Francisco, CA 94158, USA. Electronic address: Hong-Ha.Truong@ucsf.edu.

Funding

HIV Transmission Cluster Analysis to Inform PreventionR01MH096642 · NIMH · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI TRUONG, HONG-HA M · 2012 to 2016
$2.3M
NIMH NIH HHS R01 MH096642
6 · The paper itself

Abstract

The HIV-1 epidemic in the US has historically been dominated by subtype B. HIV subtype diversity has not been extensively examined in most US cities to determine whether non-B variants have become established, as has been observed in many other global regions. We describe the diversity of non-B variants and present evidence of local transmission of non-B HIV in San Francisco. Viral sequences collected from patients between 2000 and 2016 were matched to the San Francisco HIV/AIDS case registry. HIV subtype was determined using COMET. Phylogenies were reconstructed using the pol region of subtypes A, C, D, G, CRF01_AE, CRF02_AG, and CRF07_BC, with reference sequences from the LANL HIV database. Associations of non-B subtypes and circulating recombinant forms (CRFs) with patient characteristics were assessed using multivariable logistic regression. Out of 11,381 sequences, 10,669 were from 7235 registry cases, of which 141 (2%) had non-B subtypes and CRFs and 72 (1%) had unique recombinant forms. CRF01_AE (0.8%) and subtype C (0.5%) were the most prevalent non-B forms. The frequency of non-B subtypes and CRFs increased in San Francisco during years 2000-2016. Out of 146 transmission events involving non-B study sequences, 18% indicated local transmission within the study population and 74% appeared to be inward migration of the virus. Compared to 7016 cases with only subtype B, 141 cases with non-B sequences were more likely to be of non-US country of birth (aOR = 11.02; p < 0.001), of Asian/Pacific-Islander race/ethnicity (aOR = 3.17; p < 0.001), and diagnosed after 2009 (aOR = 4.81; p < 0.001). Results suggest that most non-B infections were likely acquired outside the US and that local transmission of non-B forms has occurred but so far has not produced extensive transmission networks. Thus, non-B variants were not widely established in San Francisco, an observation that differs from cities worldwide with more diverse epidemics.

Indexed as

AdultAgedFemaleHIV-1HIV InfectionsHumansMaleMiddle AgedPhylogenyPrevalenceSan FranciscoYoung AdultCirculating recombinant formsEpidemiologyHIVNon-B subtypePhylogenySan Francisco

Identifiers

PMID33321227
PMCPMC10686190

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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.