Literature DB >> 3098686

Rickettsia prowazekii requires host cell serine and glycine for growth.

F E Austin, J Turco, H H Winkler.   

Abstract

The growth requirement of Rickettsia prowazekii for the amino acids serine and glycine was assessed in both wild-type cell lines and a mutant cell line. X-irradiated L929 cells supported the growth of R. prowazekii when the cells were incubated in Eagle minimal essential medium supplemented with serum. In contrast, in this medium, X-irradiated Vero cells did not support the growth of rickettsiae unless cycloheximide, serine, or glycine was added. Other nonessential amino acids, additional glucose, and potential products of host cell metabolism of serine and glycine were nonstimulatory. The concentration of serine or glycine required to support rickettsial growth had no effect on the doubling time of uninfected, unirradiated Vero cells. A comparison of intracellular amino acid pools indicated that the serine and glycine concentrations in mock-infected Vero cells were approximately 31 and 14% of the respective concentrations in mock-infected L929 cells. The pools of both amino acids in Vero cells increased markedly upon treatment of the cells with cycloheximide. Interconversion of serine and glycine catalyzed by serine hydroxymethyltransferase was detected in cell-free extracts of purified rickettsiae. However, this enzymatic activity did not permit rickettsial growth in a glycine-requiring clone (772-56d) of the Chinese hamster ovary cell CHO-K1 in the absence of glycine supplementation. These data indicate that R. prowazekii depends on the host cell for serine or glycine.

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Year:  1987        PMID: 3098686      PMCID: PMC260309          DOI: 10.1128/iai.55.1.240-244.1987

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  25 in total

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Authors:  H E HOPPS; E B JACKSON; J X DANAUSKAS; J E SMADEL
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Authors:  J C Williams; E Weiss
Journal:  J Bacteriol       Date:  1978-06       Impact factor: 3.490

4.  Competition between Chlamydia psittaci and L cells for host isoleucine pools: a limiting factor in chlamydial multiplication.

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5.  Separation of viable Rickettsia typhi from yolk sac and L cell host components by renografin density gradient centrifugation.

Authors:  E Weiss; J C Coolbaugh; J C Williams
Journal:  Appl Microbiol       Date:  1975-09

6.  Adenine nucleotide degradation by the obligate intracellular bacterium Rickettsia typhi.

Authors:  J C Williams
Journal:  Infect Immun       Date:  1980-04       Impact factor: 3.441

7.  High performance liquid chromatographic determination of amino acids in the picomole range.

Authors:  D W Hill; F H Walters; T D Wilson; J D Stuart
Journal:  Anal Chem       Date:  1979-07       Impact factor: 6.986

8.  Enzymatic activities leading to pyrimidine nucleotide biosynthesis from cell-free extracts of Rickettsia typhi.

Authors:  J C Williams; J C Peterson
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9.  Inhibitory and restorative effects of adenine nucleotides on rickettsial adsorption and hemolysis.

Authors:  H H Winkler
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10.  Differential requirements for enriched atmospheric carbon dioxide content for intracellular growth in cell culture among selected members of the genus Rickettsia.

Authors:  A I Kopmans-Gargantiel; C L Wisseman
Journal:  Infect Immun       Date:  1981-03       Impact factor: 3.441

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6.  Proline incorporation into protein by Rickettsia prowazekii during growth in Chinese hamster ovary (CHO-K1) cells.

Authors:  F E Austin; H H Winkler
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7.  Wholly Rickettsia! Reconstructed Metabolic Profile of the Quintessential Bacterial Parasite of Eukaryotic Cells.

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