Evidence map›Paper›PMID 10456919›Full record

ArticleInfection and immunity1999

Preliminary characterization of a Mycobacterium abscessus mutant in human and murine models of infection.

T F Byrd, C R Lyons

Open access · bronzeAbstract read
In one paragraph

Article in Infection and immunity, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

112 citing papers in PubMed, 182 citations in OpenAlex.

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  13. International journal of molecular sciences · 2025
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  14. Microorganisms · 2025
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  17. Divergent host humoral innate immune response to the smooth-to-rough adaptation ofFrontiers in cellular and infection microbiology · 2025
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  18. Frontiers in cellular and infection microbiology · 2025
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52 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

T F ByrdDepartment of Medicine, Albuquerque Veterans Affairs Medical Center, Albuquerque, New Mexico 87108, USA. tfbyrd@pol.net
C R Lyons
University of New Mexico · USVeterans Health Administration · US

Funding

AEROSOL THERAPY FOR M TUBERCULOSIS INFECTIONR01HL055776 · NHLBI · UNIVERSITY OF NEW MEXICO · PI LYONS, CLIFFORD RICK · 1995 to 1999
–
IRON AND TNF IN CYTOKINE RESTRICTION OF M TUBERCULOSISR29AI035249 · NIAID · UNIVERSITY OF NEW MEXICO · PI BYRD, THOMAS F · 1993 to 1997
–
NHLBI NIH HHS HL55776NIAID NIH HHS AI35249
6 · The paper itself

Abstract

The ability to persist in the host after the establishment of infection is an important virulence determinant for mycobacteria. Mycobacterium abscessus is a rapidly growing mycobacterial species which causes a variety of clinical syndromes in humans. We have obtained a rough, wild-type human clinical isolate of M. abscessus (M. abscessus-R) and a smooth, attenuated mutant (M. abscessus-S) which spontaneously dissociated from the clinical isolate. We have found that M. abscessus-R is able to persist and multiply in a murine pulmonary infection model in contrast to M. abscessus-S, which is rapidly cleared. To understand the basis for this difference, we characterized the behavior of these variants in human tissue culture models of infection. M. abscessus-R is able to persist and multiply in human monocytes, while M. abscessus-S is deficient in this ability. Both of these variants are phagocytized by human monocytes. M. abscessus-R resides in a phagosome typical for pathogenic mycobacteria with a tightly adherent phagosomal membrane. In contrast, M. abscessus-S resides in a "loose" phagosome with the phagosomal membrane separated from the bacterial cell wall. Both M. abscessus variants also have distinctive growth patterns in a recently described fibroblast-mycobacterium microcolony assay, with M. abscessus-R exhibiting growth characteristics similar to those previously reported for virulent M. tuberculosis and M. abscessus-S exhibiting growth characteristics similar to those previously reported for avirulent M. tuberculosis. In both the monocyte infection assay and the murine pulmonary infection model, numerous infected mononuclear phagocyte aggregates develop at sites of M. abscessus-R infection, but are absent with M. abscessus-S infection. We conclude that a mutation has occurred in the M. abscessus-S variant which has altered the ability of this organism to persist and multiply in host cells and that this may be related to the phenotypic changes we have observed in our tissue culture models of infection.

Indexed as

MutationAnimalsCells, CulturedDisease Models, AnimalFemaleFibroblastsHumansLungMiceMice, Inbred BALB CMice, SCIDMonocytesMycobacterium Infections, NontuberculousNontuberculous MycobacteriaPhagosomes

Identifiers

PMID10456919
PMCPMC96797
OpenAlexW2119462342

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.