Bacillus thuringiensis: Difference between revisions

From MicrobeWiki, the student-edited microbiology resource
No edit summary
 
(133 intermediate revisions by 3 users not shown)
Line 1: Line 1:
{{Curated}}
{{Biorealm Genus}}
{{Biorealm Genus}}


[[Image:Bt1.jpeg|frame|right|Bacillus thuringiensis under a Scanning Electron Microscope]][http://textbookofbacteriology.net/Bt1.jpeg]
 
==Classification==
==Classification==


===Higher order taxa===
===Higher order taxa===
    
    
Eubacteria (kingdom); Bacteria (domain); Firmicutes (phylum); Bacilli (class); Bacillales (order); Bacillaceae (family); Bacillus (genus)[http://microbewiki.kenyon.edu/index.php/Bacillus]; Bacillus cereus group
Eubacteria (kingdom); Bacteria (domain); Firmicutes (phylum); Bacilli (class); Bacillales (order); Bacillaceae (family); [http://microbewiki.kenyon.edu/index.php/Bacillus ''Bacillus''] (genus); Bacillus cereus group


===Species===
===Species===
Line 12: Line 13:


==Description and significance==
==Description and significance==
Describe the appearance, habitat, etc. of the organism, and why it is important enough to have its genome sequencedDescribe how and where it was isolated.
''B. thuringiensis'' (Bt) is a gram-positive, soil-dwelling, spore-forming, rod-shaped bacteria. It is approximately 1 µm in width and 5 µm in length.[3][11] It grows at body temperature and produces a diamond-shaped crystal from its crystal proteins (Cry proteins) and uses it to fend off insects, predators, and other pathogens.[2]
Include a picture or two (with sources) if you can find them.


<i>B. thuringiensis</i> is a gram positive, soil-dwelling, spore-forming, rod-shaped bacteria.  It grows at body temperature and produces diamond-shaped crystal from its crystal proteins (cry proteins) and uses it to fend off insects, predators, and other pathogens.[http://extoxnet.orst.edu/pips/bacillus.htm] [http://www.bt.ucsd.edu/what_is_bt.html]
[[Image:Bt2.jpeg|thumb|Bacillus thuringiensis crystal|150px|right|<i>Bacillus thuringiensis</i> crystal[http://www.bact.wisc.edu/themicrobialworld/structure.html]]]


It's genome was completely sequenced fairly recently (February 23rd, 2007) [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=genome&cmd=Retrieve&dopt=Overview&list_uids=20524].  It is critical to have <i>B. thuringiensis'</i> genome sequenced because it has many benefits for humans in the form of agriculture.  Farmers frequently use it as a pesticide for their crops to fend off insects.  Having sequenced the entire genome, scientists can witness and determine how mutations can create different variant strains which may eventually grow stronger against antibiotic pests.  What's great about <i>B. thuringiensis</i> pesticide is that the S-layer it produces (where the Cry protein and toxins lie) has no known negative effects on humans, vertebrates, or plants.[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16391064&dopt=Abstract]
Its genome was recently sequenced (February 23rd, 2007) [11].  It is critical to have ''B. thuringiensis' ''genome sequenced because it has many benefits for humans in the form of agriculture.  ''Bt'' is the most common environmentally-friendly insecticide used and is the basis of over 90% of the pesticides available in the market today.[1] Having sequenced the entire genome, scientists can witness and determine how mutations can create different variant strains that may eventually grow stronger against agricultural pests.  In 2005, over 26 million hectares of Bt-enduced transgenic corn and cotton were planted.[10]  Many pests were exterminated because the Cry protein family has many flexible toxin variants.  ''B. thuringiensis'' pesticide S-layer (where the Cry protein and toxins lie) has no known negative effects on humans, vertebrates, or plants.  


Many studies indicate and consider ''B. thuringiensis'' and ''B. cereus'' to be one species.  However, their phenotypes greatly differ in that ''Bt'' produces crystal proteins despite the fact that crystal protein synthesis is controlled by plasmid genes which can be susceptible to loss and transmission to related bacteria.  One response is that ''Bt'' strains produce enterotoxins (toxins released by micro-organisms in the lower intestine) that are involved in ''B. cereus'' pathogenesis and therefore signifies a fine-line between the two species.[1]


==Genome structure==
''B. thuringiensis'' has a circular chromosome and a GC-content of approximately 32%~35%.  It has a genome size of between 5.2–5.8 Megabases.[11]  It is a facultative anaerobic organism (an organism that makes ATP by aerobic respiration if oxygen is present but can also switch to fermentation).  It has many plasmids and ''Bt's'' strains harbors a diverse range of plasmids that vary in number and in size (2–200kb).[14]  The self-replicating plasmids are important to the organism's lineage and lifestyle.[11]


http://pmep.cce.cornell.edu/profiles/extoxnet/24d-captan/bt-ext.html
The largest class of genes consists of the "δ-endotoxins" (from the Cry proteins), which often are produced as 130–140 kDa protein precursors in the insect gut under high-pH conditions to yield a 60–65 kDa biologically active core toxin.[1] These δ-Endotoxins are frequently expressed in recombinant cotton, potatoes, rice and corn. These "δ-endotoxins" from the plasmids may be more than 50kb long and self-transmissible via a conjugation-like mechanism.[7]


==Genome structure==
==Cell structure and metabolism==
Describe the size and content of the genomeHow many chromosomes?  Circular or linear?  Other interesting features?  What is known about its sequence?
Because ''B. thuringiensis'' is gram-positive, it has a thick cell wall that is comprised of peptidoglycan (amino acid polypeptide and a sugar). Between the cell wall and the plasma membrane is a small section called the periplasmic space which is essential for biosynthesis and protection.   
Does it have any plasmids?  Are they important to the organism's lifestyle?


<i>B. thuringiensis</i> has a circular plasmid chromosomeDue to its 2% GC-content, it has more A/G base pairs. Compared to its bacterial relatives, Bt's genome is not big at all.  It genome is only 5,475 nucleotides long, has approximately 2.4 to 5.7 million base pairs [http://www.mrc-lmb.cam.ac.uk/genomes/madanm/articles/dnashuff.htm], and consists of only seven genes: pK1S1_p1, pK1S1_p2, pK1S1_p3, pK1S1_p4, pK1S1_p5, pK1S1_p6, and pK1S1_p7. [http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=genome&cmd=Retrieve&dopt=Overview&list_uids=20524]
Most research has been focused on the Cry toxin crystalsThough they are many strains that differ in "insecticidal spectra and divergence in amino acid sequences"[20], the Cry proteins' activity is similar. The most salient Cry toxin and best studied is the Cry1 subclass.  It is comprised of three distinct domains. Domain I (residues 33 to 253) contains eight alpha-helicies and no beta-sheets. Domain II (residues 265 to 461) contains three anti-parallel beta-sheets and two short alpha-helicies. Domain III (residues 463-609) contains a beta-sandwich of two anti-parallel beta-sheets.


[[Image:Bt3.JPG|thumb|<i>Bacillus thuringiensis'</i> plasmid genome map|600px|center|<i>Bacillus thuringiensis'</i> plasmid genome map[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=genome&cmd=Retrieve&dopt=Overview&list_uids=20524]]]


==Cell structure and metabolism==
The optimal condition for the Cry toxin to grow and sporulate is in the insect's alkaline gut.[20]  This facilitates the ability to infect insect guts. The following is a summary of the life cycle of ''Bt''.  Stage I: axial filament formation; Stage II: forespore formation; Stage III: engulfment; Stage IV-VI: formation of cell wall, cortex, and spore coats accompanied by transformation of the spore nucleoid; Stage VII: spore maturation.[15]
Describe any interesting features and/or cell structures; how it gains energy; what important molecules it produces.
[[Image:Bt5.JPG|thumb|Bacillus thuringiensis crystal life cycle |350px|center|<i>Bacillus thuringiensis</i> crystal life cycle [15]]]


==Ecology==
==Ecology==
Describe any interactions with other organisms (included eukaryotes), contributions to the environment, effect on environment, etc.
Several studies have been done on animals to test the effects of ''B. thuringiensis''.  When treated with ''Bt''176, a corn hybrid strain of ''B. thuringiensis'', experiments  with broilers or laying hens showed no pathology was attributed.  Researchers discovered neither feed intake, feed conversion ratio, nor weight gain were influenced by the genetic modification of the crop.[21]  High concentrations of ''Bt'' in fish and aquatic organisms failed to show any adverse effects .  Experiments performed on other animals showed similar negative results.  Conclusion: There seems to be no adverse effects on non-target organisms when exposed to ''Bt''.[22]
 
Effects on the environment are largely considered mild.[22]  It is a soil bacterium and thrives at body temperature.[17]  When exposed to higher temperatures such as sunlight (UV light), however, its half-life greatly decreases to around 3.8 hours.  As soon as it is exposed to a warmer-than-normal medium, ''B. thuringiensis''' spores start deteriorating and lose viability within four days.  Normally, a short half-life is bad.  But in ''Bt's'' case, it is actually good in that the short half-life minimizes insect resistance.[22]  Additionally, when field tests were performed on a sample of transgenic corn, researchers discovered better protection from root damage by Western corn rootworm than by chemical pesticides.[7]


==Pathology==
==Pathology==
[[Image:Bt4.JPG|frame|How Bacillus thuringiensis kills a caterpillar|200px|right|How <i>Bacillus thuringiensis</i> kills a caterpillar[http://www.bt.ucsd.edu/how_bt_work.html]]]
Common insect targets are "moths, mosquitoes, blackflies, beetles, hoppers, aphids, wasps and bees as well as nematodes"[17][18][19].  The toxicity and virulence lies in the crystals.  The virulence of the Cry toxins is mediated by a cadherin receptor (a class of transmembrane proteins that play important roles in cell adhesion), BT-R1, which has been identified gut of many pathogenistic larvae.  Here is a rough process on how ''B. thuringiensis'' causes disease.  (1). ''B. thuringiensis'' is digested and the toxins are mixed with the high pH (basic conditions) to bind specific receptors in the gut to attack the host insect. (2). This process punches holes in the gut-lining and thus, the insect becomes weak. (3). As the gut is continuing to break down, spores begin to germinate from the toxic crystals and other bacterial pathogens start to infect the host. (4). ''B. thuringiensis'' spores are continuously weakening the host and the insect dies soon thereafter.
How does this organism cause disease? Human, animal, plant hosts? Virulence factors, as well as patient symptoms.
 
The ''Bacillus thuringiensis'' toxin is species-specific and non-pathogenic to humans.[5]  Specifically, however, ''Bt'' targets pests in the orders Lepidoptera, Coleptera, and Diptera.[18]  The Cry crystal toxins contain proteins that are highly toxic towards invertebrates but nontoxic towards vertebrates.[8]  There are different variant strains of ''B. thuringiensis'' Cry toxin that effect different hosts. Despite this variability, there is still a high degree of structural conservation among Cry toxin which suggests that "they possess a fundamental mechanism". All Cry variants follow a similar two-phase mechanism when infecting the host: (1). solubilization and proteolytic activation in the gut and (2) binding to the intestinal cells with pore formation.[9]
 
==Application to Biotechnology==
''Bacillus thuringiensis'' produces the Cry crystal toxin that attacks the gut of pests and kills them internally.  These Cry toxins are good agricultural tools for growing plants. Instead of using chemicals that may have adverse effects on humans, genetic engineers integrate the ''Bt'' toxin into the plant's genome. These ''Bt'' Cry toxins are safe for humans and kill off species of pests that are susceptible to the ''Bacillus thuringiensis'' endospore.


==Current Research==
1. Current fortune has enabled humans to thrive without many ''Bt''-resistant pests.  Eventually, however, pests will evolve and acquire resistance to ''Bt''.  Researchers at the University of California, San Diego are studying how nematodes defend themselves from bacterial attack.  Dr. Raffi Aroian and his colleagues attempt to analyze how Cry proteins interact (host-toxin interaction) with gut cells and prevent cell death.  Aroian is looking at host responses to the toxin on a genomic scale and look to discover the transcription factors that enable resistance in pests.[24]


Common insect targets are "including moths, mosquitoes, blackflies, beetles, hoppers, aphids, wasps and bees as well as nematodes"[http://microgen.ouhsc.edu/b_thuring/b_thuringiensis_home.htm].  The toxicity lies in the crystalsHere is a rough map of how <i>B. thuringiensis</i> causes disease. 
2. China is becoming a world-leader in isolating new ''Bt'' genes worldwide.  Since 1997, Chinese researchers have isolated and discovered 50 new ''Bt'' genes.  Recently, Chinese scientists have been analyzing the ''cry8''-type genes, which were toxic to a number of colopteran pests and certain scarab species.  Researchers used PCR-RFLP (Restriction Fragment Length Polymorphism - a technique in which organisms may be differentiated by analysis of patterns derived from cleavage in their DNA)[23].  Researchers created a clone, labeled it ''cry8Ca2'', and compared the clone with the known ''cry8Ca1'' geneAlthough both genes only differed by one amino acid, the biggest difference was a high toxcitiy towards larvae of the scarabaeid insects ''Anamala exoleta'' and ''Anomala corpulenta''.[4]


1. <i>B. thuringiensis</i> is digested and the toxins are mixed with the high pH to bind specific receptors in the gut to attack the host insect.  
3. It has been theorized that no known adverse environmental effects arise when crops have been spread with ''Bt''.  40% of the corn crop grown in Quebec, Cananda, uses ''Bt''. Researchers from The Environmental Management of Biotechnology for Regulation and Research and Agriculture and Agri-Food Canada want to make fully certain whether the ''Bt'' endotoxin and its gene are present in the aquatic environment and if so, in what concentrations. Researchers will also analyze the effects of Bt on the aquatic organisms of the St. Lawrence River.[25]


2. This process punches holes in the gut-lining and thus, the insect becomes weak.


3. As the gut is continuing to break down, spores begin to germinate from the toxic crystals and other bacterial pathogens start to infect the host.
==References==
[1] [http://article.pubs.nrc-cnrc.gc.ca/ppv/RPViewDoc?issn=0008-4166&volume=53&issue=3&startPage=343 Cherif, A., Ettoumi, B., Raddadi, N., Daffonchio, D., Boudabous, A. "Genomic diversity and relationship of ''Bacillus thuringiensis'' and ''Bacillus cereus'' by multi-REP-PCR fingerprinting". ''Canadian Journal of Microbiology''. 2007. Volume 53. p. 343-350.]


4. <i>B. thuringiensis</i> spores are continuously weakening the host and the insect dies soon thereafter.
[2] [http://www.jbc.org/cgi/reprint/M701314200v1 Jimenez-Juarez, N., Munoz-Garay, C., Gomez, I., Saab-Rincon, G., Damian-Alamazo, J.Y., Gill, S.S., Soberon, M., Bravo, A. "''Bacillus thuringiensis'' Cry1Ab mutants affecting oligomer formation are non toxic to ''Manduca sexta'' larvae". The Journal of biological chemistry. 2007. Ahead of print.]


<i>Bacillus thuringiensis</i> is very species-specific and does not work with every single host.  There are different strains of <i>B. thuringiensis</i> that effect different hosts. For example, "B.t. aizawai (B.t.a.) is used against wax moth larvae in honeycombs; B.t. israelensis (B.t.i.) is effective against mosquitoes", et al. The key is that the host must eat <i>B. thuringiensis</i> "in the immature, feeding stage of development referred to as larvae [because] it is ineffective against adult insects". [http://pmep.cce.cornell.edu/profiles/extoxnet/24d-captan/bt-ext.html]
[3] [http://www.jstage.jst.go.jp/article/jbb/103/4/103_381/_article Sakai, H., Howlader, M.T., Ishida, Y., Nakaguchi, A., Oka, K., Ohbayashi, K., Yamagiwa, M., Hayakawa, T. "Flexibility and strictness in functional replacement of domain III of cry insecticidal proteins from ''Bacillus thuringiensis''". Journal of bioscience and bioengineering. 2007. Volume 103. p. 381-383.]


==Application to Biotechnology==
[4] [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WJV-4NCSGXP-1&_user=4429&_coverDate=03%2F31%2F2007&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=acbbe14a9ea0b277aa7136b04127f196 Huang, D.F., Zhang, J., Song, F.P., Lang, Z.H. "Microbial control and biotechnology research on ''Bacillus thuringiensis'' in China". Journal of invertebrate pathology. 2007. Ahead of print.]
Does this organism produce any useful compounds or enzymes? What are they and how are they used?
 
[5] [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6VPN-4N2KTN2-1&_user=4429&_coverDate=04%2F30%2F2007&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=8a946d16c8b48da0e6010219f0336112 Ghelardi, E., Celandroni, F., Salvetti, S., Fiscarelli, E., Senesi S. "''Bacillus thuringiensis'' pulmonary infection: next term critical role for bacterial membrane-damaging toxins and host neutrophils". Microbes and infection / Institut Pasteur. 2007. Volume 9. p. 591-598.]
 
[6] [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T1T-4N49VPD-1&_user=4429&_coverDate=05%2F31%2F2007&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=3a2dbedb9e0e43b42a5a91ab0ed73fe5 Fortier, M., Vachon, V., Marceau, L., Schwartz, J.L., Laprade, R. "Kinetics of pore formation by the ''Bacillus thuringiensis'' toxin Cry1Ac". Biochimica et biophysica acta. 2007. Volume 1768. p. 1291-1298.]
 
[7] [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WPJ-4MWGFFP-1&_user=4429&_coverDate=06%2F30%2F2007&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=69e76c2b73abf1cb4d3db91b99c9a6d9 Huang, K.X., Badger, M., Haney, K., Evans, S.L. "Large scale production of ''Bacillus thuringiensis'' PS149B1 insecticidal proteins Cry34Ab1 and Cry35Ab1 from ''Pseudomonas fluorescens''". Protein expression and purification. 2007. Volume 53. p. 325-330.]
 
[8] [http://www.pnas.org/cgi/content/full/103/41/15154 Cappello, M., Bungiro, R.D., Harrison, L.M., Bischof, L.J., Griffitts, J.S., Barrows, B.D., Aroian, R.V. "A purified ''Bacillus thuringiensis'' crystal protein with therapeutic activity against the hookworm parasite ''Ancylostoma ceylanicum''." Proceedings of the National Academy of Sciences of the United States of America. 2006. Volume 103. p. 15154-15159.]
 
[9] [http://www3.interscience.wiley.com/cgi-bin/abstract/110493687/ABSTRACT Griffitts, J.S., Aroian, R.V. "Many roads to resistance: how invertebrates adapt to Bt toxins." BioEssays : news and reviews in molecular, cellular and developmental biology. 2005. Volume 27. p. 614-624.]
 
[10] [http://www.jbc.org/cgi/content/full/282/5/3302 Barrows, B.D., Haslam, S.M., Bischof, L.J., Morris, H.R., Dell, A., Aroian, R.V. "Resistance to ''Bacillus thuringiensis'' toxin in ''Caenorhabditis elegans'' from loss of fucose." The Journal of biological chemistry. 2007. Volume 282. p. 3302-3311.]
 
[11] [http://www.ncbi.nlm.nih.gov http://www.Pubmed.gov]
 
[12] [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T36-4CNGJKM-2&_user=4429&_coverDate=07%2F16%2F2004&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=d2f71bf1581d1a32e011af0f3af289c7 Vazquez-Padron, R.I., de la Riva, G., Aguero, G., Silva, Y., Pham, S.M., Soberon, M., Bravo, A., Aitouche, A. "Cryptic endotoxic nature of ''Bacillus thuringiensis'' Cry1Ab insecticidal crystal protein." FEBS letters. 2004. Volume 570. p. 30-36.]
 
[13] [http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=250300&blobtype=pdf Yousten, A.A., Rogoff, M.H. "Metabolism of ''Bacillus thuringiensis'' in Relation to Spore and Crystal Formation." Journal of Bacteriology. 1969. 1969. Volume 100. p. 1229-1236.]
 
[14] [http://aem.asm.org/cgi/content/full/66/1/118 Thomas, D.J., Morgan, J.A., Whipps, J.M., Saunders, J.R. "Plasmid Transfer between the ''Bacillus thuringiensis'' Subspecies ''kurstaki'' and ''tenebrionis'' in Laboratory Culture and Soil and in Lepidopteran and Coleopteran Larvae". Applied and environmental microbiology. 2000. Volume 66. p. 118-124.]
 
[15] [http://jb.asm.org/cgi/reprint/127/3/1472?view=long&pmid=182671 Bechtel, D.B., Bulla, L.A. Jr. "Electron Microscope Study of Sporulation and Parasporal Crystal Formation in ''Bacillus thuringiensis''" Journal of bacteriology. 1976. Volume 127. p. 1472-1481.]
 
[16] [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T2W-4GPVXF1-2&_user=4429&_coverDate=09%2F15%2F2005&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=b5de8e945cbfd6173348b1ec261a3707 Anderson et al. "Comparative genome analysis of ''Bacillus cereus'' group genomes with ''Bacillus subtilis''". FEMS Microbiol Letters. 2005. Volume 250. p. 175-184.]
 
[17] [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6T79-45CW05S-1&_user=4429&_coverDate=09%2F30%2F2002&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=a6e30b3199c2cd21411b5aa76a3c3ecd Dorsch et al. "Cry1A toxins of ''Bacillus thuringiensis'' bind specifically to a region adjacent to the membrane-proximal extracellular domain of BT-R(1) in ''Manduca sexta'': involvement of a cadherin in the entomopathogenicity of ''Bacillus thuringiensis''". Insect biochemistry molecular biology. 2002. Volume 32. p. 1025-1036.]


It was once thought that B. thuringiensis' method of toxology was via toxin-mediated disruption, which basically consisted of Bt killing the host by starvation or blood poison.  However, recent reserach by scientists at the University of Wisconsin-Madison reported having other players involved.[http://www.nanotechbuzz.com/50226711/bt_microbe_fools_biotech_experts.php]
[18] [http://www.jbc.org/cgi/content/abstract/270/10/5490 Vadlamudi, R., Weber, E., Inhae, J., Ji, T.H., Bulla Jr., L.A. "Cloning and expression of a receptor for an insecticidal toxin of ''Bacillus thuringiensis''". The Journal of biological chemistry. 1995. Volume 270. p. 5490-5494.]


==Current Research==
[19] [http://www.nature.com/cdd/journal/v12/n11/abs/4401675a.html;jsessionid=7760D8809460C37072206587C9863F4C Zhang, X., Candas, M., Griko, N.B., Rose-Young, L., Bulla, L.A. "Cytotoxicity of ''Bacillus thuringiensis'' Cry1Ab toxin depends on specific binding of the toxin to the cadherin receptor BT-R(1) expressed in insect cells". Cell death and differentiation. 2005. Volume 12. p. 1407-1416.]


Enter summaries of the most recent research here--at least three required
[20] [http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WK7-45S96Y4-10&_user=4429&_coverDate=12%2F01%2F1995&_rdoc=1&_fmt=&_orig=search&_sort=d&view=c&_acct=C000059602&_version=1&_urlVersion=0&_userid=4429&md5=ad1313baa544559eaa788107fe2b0c1c Grochulski, P., Masson, L., Borisova, S., Pusztai-Carey, M., Schwartz, J.L., Brousseau, R., Cygler, M. "''Bacillus thuringiensis'' CryIA(a) insecticidal toxin: crystal structure and channel formation. Journal of molecular biology". 1995. Volume 254. p. 447-467.]


1. http://www.bt.ucsd.edu/   http://biology.ucsd.edu/faculty/aroian.html
[21] [http://ps.fass.org/cgi/reprint/84/3/385 Aeschbacher, A., Messikommer, R., Melie, L., Wenk, C. "''Bt''176 corn in poultry nutrition: physiological characteristics and fate of recombinant plant DNA in chickens". Poultry science. 2005. Volume 84. p. 385-394.]


2.  
[22] [http://pubs3.acs.org/acs/journals/doilookup?in_doi=10.1021/jf040442k Clark, B.W., Phillips, T.A., Coats, J.R. Environmental Fate and Effects of ''Bacillus thuringiensis'' (Bt) Proteins from Transgenic Crops: a Review. Journal of agricultural and food chemistry. 2005. Volume 53. p. 4643-4653.]


3.
[23] [http://vm.cfsan.fda.gov/~frf/rflp.html FDA.gov info on PCR-RFLP]


==References==
[24] [http://biology.ucsd.edu/faculty/aroian.html UCSD Raffi Aroian Research]
[Sample reference] [http://ijs.sgmjournals.org/cgi/reprint/50/2/489 Takai, K., Sugai, A., Itoh, T., and Horikoshi, K. "''Palaeococcus ferrophilus'' gen. nov., sp. nov., a barophilic, hyperthermophilic archaeon from a deep-sea hydrothermal vent chimney". ''International Journal of Systematic and Evolutionary Microbiology''. 2000. Volume 50. p. 489-500.]


[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=genome&cmd=Retrieve&dopt=Overview&list_uids=20524 National Center for Biotechnology Information]
[25] [http://www.qc.ec.gc.ca/csl/pro/pro032fg_e.html Canada ''Bt'' Research]


Edited by Ernest Hsu of [mailto:ralarsen@ucsd.edu Rachel Larsen] and Kit Pogliano
Edited by Ernest Hsu of [mailto:ralarsen@ucsd.edu Rachel Larsen] and Kit Pogliano

Latest revision as of 19:21, 22 April 2011

This is a curated page. Report corrections to Microbewiki.

A Microbial Biorealm page on the genus Bacillus thuringiensis


Classification

Higher order taxa

Eubacteria (kingdom); Bacteria (domain); Firmicutes (phylum); Bacilli (class); Bacillales (order); Bacillaceae (family); Bacillus (genus); Bacillus cereus group

Species

Bacillus thuringiensis

Description and significance

B. thuringiensis (Bt) is a gram-positive, soil-dwelling, spore-forming, rod-shaped bacteria. It is approximately 1 µm in width and 5 µm in length.[3][11] It grows at body temperature and produces a diamond-shaped crystal from its crystal proteins (Cry proteins) and uses it to fend off insects, predators, and other pathogens.[2]


Its genome was recently sequenced (February 23rd, 2007) [11]. It is critical to have B. thuringiensis' genome sequenced because it has many benefits for humans in the form of agriculture. Bt is the most common environmentally-friendly insecticide used and is the basis of over 90% of the pesticides available in the market today.[1] Having sequenced the entire genome, scientists can witness and determine how mutations can create different variant strains that may eventually grow stronger against agricultural pests. In 2005, over 26 million hectares of Bt-enduced transgenic corn and cotton were planted.[10] Many pests were exterminated because the Cry protein family has many flexible toxin variants. B. thuringiensis pesticide S-layer (where the Cry protein and toxins lie) has no known negative effects on humans, vertebrates, or plants.

Many studies indicate and consider B. thuringiensis and B. cereus to be one species. However, their phenotypes greatly differ in that Bt produces crystal proteins despite the fact that crystal protein synthesis is controlled by plasmid genes which can be susceptible to loss and transmission to related bacteria. One response is that Bt strains produce enterotoxins (toxins released by micro-organisms in the lower intestine) that are involved in B. cereus pathogenesis and therefore signifies a fine-line between the two species.[1]

Genome structure

B. thuringiensis has a circular chromosome and a GC-content of approximately 32%~35%. It has a genome size of between 5.2–5.8 Megabases.[11] It is a facultative anaerobic organism (an organism that makes ATP by aerobic respiration if oxygen is present but can also switch to fermentation). It has many plasmids and Bt's strains harbors a diverse range of plasmids that vary in number and in size (2–200kb).[14] The self-replicating plasmids are important to the organism's lineage and lifestyle.[11]

The largest class of genes consists of the "δ-endotoxins" (from the Cry proteins), which often are produced as 130–140 kDa protein precursors in the insect gut under high-pH conditions to yield a 60–65 kDa biologically active core toxin.[1] These δ-Endotoxins are frequently expressed in recombinant cotton, potatoes, rice and corn. These "δ-endotoxins" from the plasmids may be more than 50kb long and self-transmissible via a conjugation-like mechanism.[7]

Cell structure and metabolism

Because B. thuringiensis is gram-positive, it has a thick cell wall that is comprised of peptidoglycan (amino acid polypeptide and a sugar). Between the cell wall and the plasma membrane is a small section called the periplasmic space which is essential for biosynthesis and protection.

Most research has been focused on the Cry toxin crystals. Though they are many strains that differ in "insecticidal spectra and divergence in amino acid sequences"[20], the Cry proteins' activity is similar. The most salient Cry toxin and best studied is the Cry1 subclass. It is comprised of three distinct domains. Domain I (residues 33 to 253) contains eight alpha-helicies and no beta-sheets. Domain II (residues 265 to 461) contains three anti-parallel beta-sheets and two short alpha-helicies. Domain III (residues 463-609) contains a beta-sandwich of two anti-parallel beta-sheets.


The optimal condition for the Cry toxin to grow and sporulate is in the insect's alkaline gut.[20] This facilitates the ability to infect insect guts. The following is a summary of the life cycle of Bt. Stage I: axial filament formation; Stage II: forespore formation; Stage III: engulfment; Stage IV-VI: formation of cell wall, cortex, and spore coats accompanied by transformation of the spore nucleoid; Stage VII: spore maturation.[15]

Bacillus thuringiensis crystal life cycle [15]

Ecology

Several studies have been done on animals to test the effects of B. thuringiensis. When treated with Bt176, a corn hybrid strain of B. thuringiensis, experiments with broilers or laying hens showed no pathology was attributed. Researchers discovered neither feed intake, feed conversion ratio, nor weight gain were influenced by the genetic modification of the crop.[21] High concentrations of Bt in fish and aquatic organisms failed to show any adverse effects . Experiments performed on other animals showed similar negative results. Conclusion: There seems to be no adverse effects on non-target organisms when exposed to Bt.[22]

Effects on the environment are largely considered mild.[22] It is a soil bacterium and thrives at body temperature.[17] When exposed to higher temperatures such as sunlight (UV light), however, its half-life greatly decreases to around 3.8 hours. As soon as it is exposed to a warmer-than-normal medium, B. thuringiensis' spores start deteriorating and lose viability within four days. Normally, a short half-life is bad. But in Bt's case, it is actually good in that the short half-life minimizes insect resistance.[22] Additionally, when field tests were performed on a sample of transgenic corn, researchers discovered better protection from root damage by Western corn rootworm than by chemical pesticides.[7]

Pathology

Common insect targets are "moths, mosquitoes, blackflies, beetles, hoppers, aphids, wasps and bees as well as nematodes"[17][18][19]. The toxicity and virulence lies in the crystals. The virulence of the Cry toxins is mediated by a cadherin receptor (a class of transmembrane proteins that play important roles in cell adhesion), BT-R1, which has been identified gut of many pathogenistic larvae. Here is a rough process on how B. thuringiensis causes disease. (1). B. thuringiensis is digested and the toxins are mixed with the high pH (basic conditions) to bind specific receptors in the gut to attack the host insect. (2). This process punches holes in the gut-lining and thus, the insect becomes weak. (3). As the gut is continuing to break down, spores begin to germinate from the toxic crystals and other bacterial pathogens start to infect the host. (4). B. thuringiensis spores are continuously weakening the host and the insect dies soon thereafter.

The Bacillus thuringiensis toxin is species-specific and non-pathogenic to humans.[5] Specifically, however, Bt targets pests in the orders Lepidoptera, Coleptera, and Diptera.[18] The Cry crystal toxins contain proteins that are highly toxic towards invertebrates but nontoxic towards vertebrates.[8] There are different variant strains of B. thuringiensis Cry toxin that effect different hosts. Despite this variability, there is still a high degree of structural conservation among Cry toxin which suggests that "they possess a fundamental mechanism". All Cry variants follow a similar two-phase mechanism when infecting the host: (1). solubilization and proteolytic activation in the gut and (2) binding to the intestinal cells with pore formation.[9]

Application to Biotechnology

Bacillus thuringiensis produces the Cry crystal toxin that attacks the gut of pests and kills them internally. These Cry toxins are good agricultural tools for growing plants. Instead of using chemicals that may have adverse effects on humans, genetic engineers integrate the Bt toxin into the plant's genome. These Bt Cry toxins are safe for humans and kill off species of pests that are susceptible to the Bacillus thuringiensis endospore.

Current Research

1. Current fortune has enabled humans to thrive without many Bt-resistant pests. Eventually, however, pests will evolve and acquire resistance to Bt. Researchers at the University of California, San Diego are studying how nematodes defend themselves from bacterial attack. Dr. Raffi Aroian and his colleagues attempt to analyze how Cry proteins interact (host-toxin interaction) with gut cells and prevent cell death. Aroian is looking at host responses to the toxin on a genomic scale and look to discover the transcription factors that enable resistance in pests.[24]

2. China is becoming a world-leader in isolating new Bt genes worldwide. Since 1997, Chinese researchers have isolated and discovered 50 new Bt genes. Recently, Chinese scientists have been analyzing the cry8-type genes, which were toxic to a number of colopteran pests and certain scarab species. Researchers used PCR-RFLP (Restriction Fragment Length Polymorphism - a technique in which organisms may be differentiated by analysis of patterns derived from cleavage in their DNA)[23]. Researchers created a clone, labeled it cry8Ca2, and compared the clone with the known cry8Ca1 gene. Although both genes only differed by one amino acid, the biggest difference was a high toxcitiy towards larvae of the scarabaeid insects Anamala exoleta and Anomala corpulenta.[4]

3. It has been theorized that no known adverse environmental effects arise when crops have been spread with Bt. 40% of the corn crop grown in Quebec, Cananda, uses Bt. Researchers from The Environmental Management of Biotechnology for Regulation and Research and Agriculture and Agri-Food Canada want to make fully certain whether the Bt endotoxin and its gene are present in the aquatic environment and if so, in what concentrations. Researchers will also analyze the effects of Bt on the aquatic organisms of the St. Lawrence River.[25]


References

[1] Cherif, A., Ettoumi, B., Raddadi, N., Daffonchio, D., Boudabous, A. "Genomic diversity and relationship of Bacillus thuringiensis and Bacillus cereus by multi-REP-PCR fingerprinting". Canadian Journal of Microbiology. 2007. Volume 53. p. 343-350.

[2] Jimenez-Juarez, N., Munoz-Garay, C., Gomez, I., Saab-Rincon, G., Damian-Alamazo, J.Y., Gill, S.S., Soberon, M., Bravo, A. "Bacillus thuringiensis Cry1Ab mutants affecting oligomer formation are non toxic to Manduca sexta larvae". The Journal of biological chemistry. 2007. Ahead of print.

[3] Sakai, H., Howlader, M.T., Ishida, Y., Nakaguchi, A., Oka, K., Ohbayashi, K., Yamagiwa, M., Hayakawa, T. "Flexibility and strictness in functional replacement of domain III of cry insecticidal proteins from Bacillus thuringiensis". Journal of bioscience and bioengineering. 2007. Volume 103. p. 381-383.

[4] Huang, D.F., Zhang, J., Song, F.P., Lang, Z.H. "Microbial control and biotechnology research on Bacillus thuringiensis in China". Journal of invertebrate pathology. 2007. Ahead of print.

[5] Ghelardi, E., Celandroni, F., Salvetti, S., Fiscarelli, E., Senesi S. "Bacillus thuringiensis pulmonary infection: next term critical role for bacterial membrane-damaging toxins and host neutrophils". Microbes and infection / Institut Pasteur. 2007. Volume 9. p. 591-598.

[6] Fortier, M., Vachon, V., Marceau, L., Schwartz, J.L., Laprade, R. "Kinetics of pore formation by the Bacillus thuringiensis toxin Cry1Ac". Biochimica et biophysica acta. 2007. Volume 1768. p. 1291-1298.

[7] Huang, K.X., Badger, M., Haney, K., Evans, S.L. "Large scale production of Bacillus thuringiensis PS149B1 insecticidal proteins Cry34Ab1 and Cry35Ab1 from Pseudomonas fluorescens". Protein expression and purification. 2007. Volume 53. p. 325-330.

[8] Cappello, M., Bungiro, R.D., Harrison, L.M., Bischof, L.J., Griffitts, J.S., Barrows, B.D., Aroian, R.V. "A purified Bacillus thuringiensis crystal protein with therapeutic activity against the hookworm parasite Ancylostoma ceylanicum." Proceedings of the National Academy of Sciences of the United States of America. 2006. Volume 103. p. 15154-15159.

[9] Griffitts, J.S., Aroian, R.V. "Many roads to resistance: how invertebrates adapt to Bt toxins." BioEssays : news and reviews in molecular, cellular and developmental biology. 2005. Volume 27. p. 614-624.

[10] Barrows, B.D., Haslam, S.M., Bischof, L.J., Morris, H.R., Dell, A., Aroian, R.V. "Resistance to Bacillus thuringiensis toxin in Caenorhabditis elegans from loss of fucose." The Journal of biological chemistry. 2007. Volume 282. p. 3302-3311.

[11] http://www.Pubmed.gov

[12] Vazquez-Padron, R.I., de la Riva, G., Aguero, G., Silva, Y., Pham, S.M., Soberon, M., Bravo, A., Aitouche, A. "Cryptic endotoxic nature of Bacillus thuringiensis Cry1Ab insecticidal crystal protein." FEBS letters. 2004. Volume 570. p. 30-36.

[13] Yousten, A.A., Rogoff, M.H. "Metabolism of Bacillus thuringiensis in Relation to Spore and Crystal Formation." Journal of Bacteriology. 1969. 1969. Volume 100. p. 1229-1236.

[14] Thomas, D.J., Morgan, J.A., Whipps, J.M., Saunders, J.R. "Plasmid Transfer between the Bacillus thuringiensis Subspecies kurstaki and tenebrionis in Laboratory Culture and Soil and in Lepidopteran and Coleopteran Larvae". Applied and environmental microbiology. 2000. Volume 66. p. 118-124.

[15] Bechtel, D.B., Bulla, L.A. Jr. "Electron Microscope Study of Sporulation and Parasporal Crystal Formation in Bacillus thuringiensis" Journal of bacteriology. 1976. Volume 127. p. 1472-1481.

[16] Anderson et al. "Comparative genome analysis of Bacillus cereus group genomes with Bacillus subtilis". FEMS Microbiol Letters. 2005. Volume 250. p. 175-184.

[17] Dorsch et al. "Cry1A toxins of Bacillus thuringiensis bind specifically to a region adjacent to the membrane-proximal extracellular domain of BT-R(1) in Manduca sexta: involvement of a cadherin in the entomopathogenicity of Bacillus thuringiensis". Insect biochemistry molecular biology. 2002. Volume 32. p. 1025-1036.

[18] Vadlamudi, R., Weber, E., Inhae, J., Ji, T.H., Bulla Jr., L.A. "Cloning and expression of a receptor for an insecticidal toxin of Bacillus thuringiensis". The Journal of biological chemistry. 1995. Volume 270. p. 5490-5494.

[19] Zhang, X., Candas, M., Griko, N.B., Rose-Young, L., Bulla, L.A. "Cytotoxicity of Bacillus thuringiensis Cry1Ab toxin depends on specific binding of the toxin to the cadherin receptor BT-R(1) expressed in insect cells". Cell death and differentiation. 2005. Volume 12. p. 1407-1416.

[20] Grochulski, P., Masson, L., Borisova, S., Pusztai-Carey, M., Schwartz, J.L., Brousseau, R., Cygler, M. "Bacillus thuringiensis CryIA(a) insecticidal toxin: crystal structure and channel formation. Journal of molecular biology". 1995. Volume 254. p. 447-467.

[21] Aeschbacher, A., Messikommer, R., Melie, L., Wenk, C. "Bt176 corn in poultry nutrition: physiological characteristics and fate of recombinant plant DNA in chickens". Poultry science. 2005. Volume 84. p. 385-394.

[22] Clark, B.W., Phillips, T.A., Coats, J.R. Environmental Fate and Effects of Bacillus thuringiensis (Bt) Proteins from Transgenic Crops: a Review. Journal of agricultural and food chemistry. 2005. Volume 53. p. 4643-4653.

[23] FDA.gov info on PCR-RFLP

[24] UCSD Raffi Aroian Research

[25] Canada Bt Research

Edited by Ernest Hsu of Rachel Larsen and Kit Pogliano