Literature DB >> 1847313

In vitro myelosuppressive effects of the parvovirus minute virus of mice (MVMi) on hematopoietic stem and committed progenitor cells.

J C Segovia1, A Real, J A Bueren, J M Almendral.   

Abstract

The interaction of two strains of the parvovirus minute virus of mice (MVM) with the mouse hematopoietic system has been studied. The immunosuppressive strain MVMi, but not the prototype virus MVMp, inhibited hematopoiesis in vitro, as judged by colony-forming assays of the erythroid burst-forming unit and granulocyte-monocyte colony-forming unit (CFU-GM) progenitors. Interestingly, primitive hematopoietic cells of the stem compartment (CFU-S12d), were equally susceptible to the MVMi cytotoxic infection, unravelling an unprecedented feature of virus-hematopoiesis interactions. The replication of both strains of MVM virus was evaluated in primary myeloid cells of long-term bone marrow cultures. A high viral DNA synthesis and maturation was observed in MVMi-infected myeloid cells, but it was undetectable in MVMp infections; moreover, the expression of the cytotoxic nonstructural NS-1 protein, a more reliable parameter of cell permissiveness to MVM infection, was only detected in MVMi-infected cells. Correspondingly, MVMi was propagated to high titers of infectious virus and it mediated an acute myelosuppression in these cultures. We conclude that MVMi has a wider tropism than was previously suspected and it is proposed that cytotoxic infection of hematopoietic stem cells, besides that of committed progenitors, may provide an additional basis to understand the pathogenesis of certain animal and human bone marrow failures of viral etiology.

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Year:  1991        PMID: 1847313

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  21 in total

1.  A field strain of minute virus of mice (MVMm) exhibits age- and strain-specific pathogenesis.

Authors:  Rachel D Brownlee; Amir Ardeshir; Michael D Becker; April M Wagner; David G Besselsen
Journal:  J Gen Virol       Date:  2018-03-08       Impact factor: 3.891

2.  Parvovirus minute virus of mice strain i multiplication and pathogenesis in the newborn mouse brain are restricted to proliferative areas and to migratory cerebellar young neurons.

Authors:  J C Ramírez; A Fairén; J M Almendral
Journal:  J Virol       Date:  1996-11       Impact factor: 5.103

3.  Virulent variants emerging in mice infected with the apathogenic prototype strain of the parvovirus minute virus of mice exhibit a capsid with low avidity for a primary receptor.

Authors:  Mari-Paz Rubio; Alberto López-Bueno; José M Almendral
Journal:  J Virol       Date:  2005-09       Impact factor: 5.103

4.  Myeloid depression follows infection of susceptible newborn mice with the parvovirus minute virus of mice (strain i).

Authors:  J C Segovia; J A Bueren; J M Almendral
Journal:  J Virol       Date:  1995-05       Impact factor: 5.103

5.  Severe leukopenia and dysregulated erythropoiesis in SCID mice persistently infected with the parvovirus minute virus of mice.

Authors:  J C Segovia; J M Gallego; J A Bueren; J M Almendral
Journal:  J Virol       Date:  1999-03       Impact factor: 5.103

6.  Parvovirus infection suppresses long-term repopulating hematopoietic stem cells.

Authors:  José C Segovia; Guillermo Guenechea; Jesús M Gallego; José M Almendral; Juan A Bueren
Journal:  J Virol       Date:  2003-08       Impact factor: 5.103

7.  Protein species of the parvovirus minute virus of mice strain MVMp: involvement of phosphorylated VP-2 subtypes in viral morphogenesis.

Authors:  J F Santarén; J C Ramírez; J M Almendral
Journal:  J Virol       Date:  1993-09       Impact factor: 5.103

8.  The pathogenesis of infection with minute virus of mice depends on expression of the small nonstructural protein NS2 and on the genotype of the allotropic determinants VP1 and VP2.

Authors:  D G Brownstein; A L Smith; E A Johnson; D J Pintel; L K Naeger; P Tattersall
Journal:  J Virol       Date:  1992-05       Impact factor: 5.103

9.  High mutant frequency in populations of a DNA virus allows evasion from antibody therapy in an immunodeficient host.

Authors:  Alberto López-Bueno; Mauricio G Mateu; José M Almendral
Journal:  J Virol       Date:  2003-02       Impact factor: 5.103

10.  Enhanced cytoplasmic sequestration of the nuclear export receptor CRM1 by NS2 mutations developed in the host regulates parvovirus fitness.

Authors:  Alberto López-Bueno; Noelia Valle; Jesús M Gallego; Joel Pérez; José M Almendral
Journal:  J Virol       Date:  2004-10       Impact factor: 5.103

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