Identification of genes
View Patent ↗A method for identifying a microorganism having a reduced adaptation to a particular environment comprising the steps of: (1) providing a plurality of microorganisms each of which is independently mutated by the insertional inactivation of a gene with a nucleic acid comprising a unique marker sequence so that each mutant contains a different marker sequence, or clones of the said microorganism; (2) providing individually a stored sample of each mutant produced by step (1) and providing individually stored nucleic acid comprising the unique marker sequence from each individual mutant; (3) introducing a plurality of mutants produced by step (1) into the said particular environment and allowing those microorganisms which are able to do so to grow in the said environment; (4) retrieving microorganisms from the said environment or a selected part thereof and isolating the nucleic acid from the retrieved microorganisms; (5) comparing any marker sequences in the nucleic acid isolated in step (4) to the unique marker sequence of each individual mutant stored as in step (2); and (6) selecting an individual mutant which does not contain any of the marker sequences as isolated in step (4).
1. A method for identifying a mutant microorganism having a reduced adaptation to a particular environment comprising the steps of
(a) providing a plurality of mutant microorganisms wherein each mutant microorganism contains an insertional mutation which incorporates a different marker sequence in a gene of the genome of the microorganism;
(b) introducing the plurality of mutants of step (a) into the said particular environment and allowing those microorganisms which are able to do so to grow in the said environment;
(c) retrieving microorganisms from the said environment or a selected part thereof; and
(d) selecting an individual mutant having a reduced capacity to proliferate in the particular environment by comparing marker sequences, if any, in the nucleic acid present in the retrieved microorganisms in step (c) to the different marker sequences referred to in step (a).
2. The method according to claim 1 further comprising after step (a),
removing auxotrophs from the plurality of mutant microorganisms.
3. The method of claim 1 for identifying a gene which allows a microorganism to adapt to a particular environment further comprising the step:
(e) identifying the gene which is mutated in the individual mutant having a reduced capacity to proliferate in the particular environment.
4. The method of claim 3 for isolating a gene which allows a microorganism to adapt to a particular environment further comprising the step:
(f) isolating from a wild-type microorganism the corresponding wild-type gene.
5. The method of claim 4 wherein the particular environment is a differentiated multicellular organism.
6. The method of claim 5 wherein the multicellular organism is a plant.
7. The method of claim 6 wherein the microorganism is a bacterium pathogenic to plants.
8. The method of claim 6 wherein the microorganism is a fungus pathogenic to plants.
9. The method of claim 5 wherein the multicellular organism is a non-human animal.
10. The method of claim 9 wherein the animal is selected from the group consisting of a mouse, rat, rabbit, dog and monkey.
11. The method of claim 10 wherein the animal is a mouse.
12. The method of claim 9 wherein the microorganisms is a fungus pathogenic to animals.
13. The method of claim 12 wherein the fungus is selected from the group consisting of Aspergillus spp., Cryptococcus neoformans and Histoplasma capsulatum.
14. The method of claim 9 wherein in step (b) the microorganisms are introduced orally, intravenously, intranasally, or intraperitoneally.
15. The method of claim 14 wherein in step (c) the microorganisms are retrieved from the spleen.
16. The method of claim 9 wherein the microorganism is a bacterium pathogenic to animals.
17. The method of claim 16 wherein the bacterium is selected from the group consisting of Bordetella pertussis, Campylobacter jejuni Clostridium botulinum, Escherichia coli, Haemophilus decreyi Haemophilus influenzae, Helicobacter pylori, Klebsiella pneumoniae, Legionella pneumophila, Listeria spp., Neisseria gonorrhoeae, Neisseria meningitidis, Pseudomonas spp., Salmonella spp., Shigella spp., Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae, Vibrio spp., and Yersinia pestis.
18. The method of claim 5 wherein in step (c) the microorganisms are retrieved from the said environment at a site remote from the site of introduction in step (b).
19. The method of claim 1 wherein the microorganism is a bacterium.
20. The method of claim 1 wherein the microorganism is a fungus.
21. The method of claim 1 wherein in step (d) the comparison of any marker sequences in the nucleic acid of the mutants retrieved in step (c) to the marker sequences referred to in step (a) uses DNA amplification techniques and oligonucleotide primers.