Campylobacter fetus: Difference between revisions

From MicrobeWiki, the student-edited microbiology resource
No edit summary
 
(26 intermediate revisions by 3 users not shown)
Line 1: Line 1:
{{Curated}}
{{Biorealm Genus}}
{{Biorealm Genus}}
[[image:Campylobacterfetus.jpg|caption|right|frame|thumbnail|http://www.usda.gov/oc/photo/99cs0650.htm]]
[[image:Campylobacterfetus.jpg|caption|right|frame|thumbnail|http://www.usda.gov/oc/photo/99cs0650.htm]]
Line 8: Line 9:
===Higher order taxa===
===Higher order taxa===


  Bacteria; Proteobacteria; Epsilon Proteobacteria; Campylobacterales; Campylobacteraceae; Campylobacter''
  Bacteria; Proteobacteria; Epsilon Proteobacteria; Campylobacterales; Campylobacteraceae; Campylobacter


===Species===  
===Species===  
Line 23: Line 24:


==Description and significance==
==Description and significance==
Campylobacter fetus is a spiral slender, spirally curved bacterial pathogen, enclosed with an S layer of special crystalline surface proteins. (Their unique function will be discussed later) . It is a gram negative species holding two membranes and a thin cell wall in between. Since it is a pathogen, it can reside anywhere in the human body. The campylobacter S layer proteins were found to have a virulence factor in resistance to the host immune defense mechanisms. Two subspecies were then suspected to exist in the campylobacter. One was Campylobacter fetus subsp. fetus and Campylobacter fetus subsp. Venerealis. To further investigate the genetic diversity among C. fetus strains of different origins, multiple genetic analyzing were used such as polymorphic DNA (RAPD), pulsed-field gel electrophoresis (PFGE), and DNA-DNA hybridization. I t was also mainly found that its natural habitat of C. fetus subsp. fetus is the intestinal tract of cattle, but it can also cause abortions.
''Campylobacter fetus'' is a slender, spirally curved bacterial pathogen, enclosed with an S layer of special crystalline surface proteins. (Their unique function will be discussed later) . It is a gram-negative species holding two membranes and a thin cell wall in between. It is a pathogen, and can reside anywhere in the human body. The ''Campylobacter fetus'' S layer proteins were found to have a virulence factor in resistance to the host immune defense mechanisms (5). According to the Journal of Clinical microbiology, (2) Two subspecies were then suspected to exist in the ''Campylobacter fetus''. One was ''Campylobacter fetus subsp. fetus'' and ''Campylobacter fetus subsp. Venerealis''. To further investigate the genetic diversity among ''C. fetus'' strains of different origins, multiple genetic analyses were used such as polymorphic DNA (RAPD), pulsed-field gel electrophoresis (PFGE), and DNA-DNA hybridization. (3) It was also mainly found that its natural habitat of ''C. fetus subsp. fetus'' is the intestinal tract of cattle, but it can also cause abortions.


==Genome structure==
==Genome structure==
''Campylobacter Fetus'' was completely sequences and was found to have 1820 genes. It has a circular DNA. Its genome length is 1,773,615 nt.GC content is 33%, coding sequence is 90%.It as 3441 proteins.  
''Campylobacter fetus'' was completely sequenced and was found to have 1820 genes. It has a circular DNA. Its genome length is 1,773,615 nt. GC content is 33%, coding sequence is 90%.It as 3441 proteins(7).The two strains that were found were divided based on their lipopolysaccharide (LPS) composition. These unique strains must contain conserved sequences so to check their unique versus mutual sequences we used gel electrophoresis. This helped answer the unique method of this pathogen in changing its S layer proteins.
The two stains that were found were dividing based on their lipopolysaccharide (LPS) composition. These unique stains must contain conserved sequences so to check their unique versus mutual sequences we used gel electrophoresis. This helped answer the unique method of this pathogen in changing its S layer proteins.
A different study (5) reported the different multiple highly conserved S layer homologous proteins, that are tightly packed in this species. These special S layer proteins are of the sizes of  97-149 kDa. They attach to the N terminus of the cell wall lipopolysaccharide non covalently. The genome holds one promoter for these proteins; it has at least one open frame and a DNA inversion.  
Different study reported the different multiple somewhat homologous and highly conserved surface layer proteins, tightly packed in this species. They encode for the 97-149 kDa. They attach to the N terminus of the cell wall lipopolysaccharide non covalently.


==Cell structure and metabolism==
==Cell structure and metabolism==
It has flagella for motility using the proton motive force for energy. Since it is a gram negative, it has three layer of protection – inner membrane, thin murien layer and an outer membrane. This organism has the optimal growth at atmospheres enriched with CO2 and 5% oxygen with nitrogen or hydrogen (journal of bacteriology). Camplylobacter needs an anaerobic environment for growth. It needs a respiratory type of metabolism for growth. These bacteria do not ferment; they also do not oxidize carbohydrates. Their entire energy is produced by certain amino acids and the tricarboxlic acid cycle intermediates.  
It has flagella for motility using the proton motive force for energy. Since it is gram-negative, it has three layer of protection – inner membrane, thin murein layer and an outer membrane. This organism has the optimal growth at atmospheres enriched with CO2 and 5% oxygen with nitrogen or hydrogen according to the journal of bacteriology(2). ''Camplylobacter fetus'' needs an anaerobic environment for growth. It needs a respiratory type of metabolism for growth. These bacteria do not ferment; they also do not oxidize carbohydrates. Their entire energy is produced by certain amino acids and the tricarboxlic acid cycle intermediates. Their special features are their unique S layer surface proteins.
As mentioned before their special features are their unique s layer surface proteins that will be discussed more elaborately on the pathogenic subtitle.


==Ecology==
==Ecology==
Campylobacter has been studied and shown to adhere to those intestinal epithelial cell lines that it invades in humans. The information from this study reported in the Canadian Journal of microbiology (1) shows that this campylobacter showed capabilities of adhering to many cell lines. This is just one example of the kind of cells this bacterium interacts with. Since this is a pathogen it interacts with many host cells either in humans or in animals mostly cattle.
''Campylobacter fetus'' has been studied and shown to adhere to those intestinal epithelial cell lines that it invades in humans. The information from this study reported in the Canadian Journal of Microbiology (1) shows that this ''Campylobacter fetus'' showed capabilities of adhering to many cell lines. This is just one example of the kind of cells this bacterium interacts with. Since this is a pathogen it interacts with many host cells either in humans or in animals mostly cattle.


==Pathology==
==Pathology==
''Campylbacter fetus'' is a bacterium that can interact and disrupt reproduction cycles. Since they have many possible surface layer proteins they have an antigenic variation that can trick the immune system. There are two types of mechanism in which these bacteria infect since there are two subspecies. The Campylobacter fetus subsp. Venerealis is found on bull mucus layer over the crypt cell layer of the male prepuce. This way, the bacteria is transmitted to the female cattle and causes its infertility. This is also the way it will be transferred again during mating. Campylobacter fetus subsp. Fetus is using a different infection mechanism in which the animal whether bird, reptile ingested the bacteria, invades the mucus cell and can cause an abortion. The two subspecies uses different ways to invade the host. Humans are mostly not affected but can accidently ingest the Campylobacter fetus subsp. Fetus and suffer sever consciousness such as inflammation of intestinal tract.(5)
''Campylobacter fetus'' is a bacterium that can interact and disrupt reproduction cycles. Since they have many possible surface layer proteins they have an antigenic variation that can trick the immune system. There are two types of mechanism by which these bacteria infect since there are two subspecies. The ''Campylobacter fetus subsp. Venerealis'' is found on bull mucus layer over the crypt cell layer of the male prepuce. This way, the bacteria is transmitted to the female cattle and causes its infertility. This is also the way it will get transferred again during mating. ''Campylobacter fetus subsp. Fetus'' is using a different infection mechanism in which the animal whether bird, reptile ingest the bacteria, it invades the mucus cell and can cause an abortion. The two subspecies uses different ways to invade the host. Humans are mostly not affected but can accidentally ingest the ''Campylobacter fetus subsp. Fetus'' and suffer severe symptoms such as inflammation of intestinal tract.(5)


==Application to Biotechnology==
==Application to Biotechnology==
Does this organism produce any useful compounds or enzymes?  What are they and how are they used?
Not applicable for this species.


==Current Research==
==Current Research==


Enter summaries of the most recent research here--at least three required
*Extensive research is being done through the years as well as in current times dealing with the big mystery of the S layer proteins that escape the immune system. Dr. Thompson (9)
Suggest two mechanisms for this. One is the resistance to the non-immune serum by preventing the binding of this serum to the ''C. fetus'' cell surface proteins. Another way might be the one I already mentioned about varying its S layer coat proteins thus avoid the antibodies of the immune system.
*Another recent finding was made by Briedis (4) in which blood from a patient with cellulites showed evidence of ''C. fetus''. Later on in testing, he found evidence for the other strain ''Venerealis''. He continued with testing to show that the strains differ in their 1% glycine tolerance. More research was done by him to finalize the results and come with a more conclusive result as to what strain appeared in his patient.
*To find more about the two different strains of ''Campylobacter fetus'', Schulze (3) conducted some tests to examine the main differences between the two strains.  He didn’t find more than what was already known of the two subspecies but ran results that gave more light for the main differences using some tests as PCR, temperature sensitivity, phenotype and genotype testing as well as many more.


==References==
==References==
1. Lori L Graham, “Campylobacter fetus adheres to and enters INT 407 cells”  
1. Lori L Graham, “Campylobacter fetus adheres to and enters INT 407 cells”  
Canadian Journal of Microbiology 48 pp 995-1007
Canadian Journal of Microbiology 48 pp 995-1007
http://rparticle.web-p.cisti.nrc.ca/rparticle/AbstractTemplateServlet?journal=cjm&volume=48&year=&issue=&msno=w02-096&calyLang=fra


2. G M Carlone and J Lascelles, “Aerobic and anaerobic respiratory systems in Campylobacter fetus subsp. jejuni grown in atmospheres containing hydrogen.”
2. G M Carlone and J Lascelles, “Aerobic and anaerobic respiratory systems in Campylobacter fetus subsp. jejuni grown in atmospheres containing hydrogen”
Journal of Bacteriology, 1982 October; 152(1): 306–314.
Journal of Bacteriology, 1982 October; 152(1): 306–314.
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=221406


3. Frank Schulze, Audrey Bagon, Wolfgang Müller, and Helmut Hotzel,
3. Frank Schulze, Audrey Bagon, Wolfgang Müller, and Helmut Hotzel,
“Identification of Campylobacter fetus Subspecies by Phenotypic Differentiation and PCR”
“Identification of Campylobacter fetus Subspecies by Phenotypic Differentiation and PCR”
Journal of Clinical Microbiology 2006 June; 44(6): 2019–2024.  
Journal of Clinical Microbiology 2006 June; 44(6): 2019–2024.  
http://jcm.asm.org/cgi/content/abstract/44/6/2019


4. Dalius J. Briedis, Ali Khamessan, Richard W. McLaughlin, Hojatollah Vali, Maria Panaritou, and Eddie C. S. Chan,
4. Dalius J. Briedis, Ali Khamessan, Richard W. McLaughlin, Hojatollah Vali, Maria Panaritou, and Eddie C. S. Chan,
“Isolation of Campylobacter fetus subsp. fetus from a Patient with Cellulitis”
“Isolation of Campylobacter fetus subsp. fetus from a Patient with Cellulitis”
Journal of Clinical Microbiology, December 2002, p. 4792-4796, Vol. 40, No. 12
Journal of Clinical Microbiology, December 2002, p. 4792-4796, Vol. 40, No. 12
http://jcm.asm.org/cgi/content/full/40/12/4792


5. Joel Dworkin & Martin J. Blaser, “Molecular mechanisms of Campylobacter fetus surface layer protein expression.”
5. Joel Dworkin & Martin J. Blaser, “Molecular mechanisms of Campylobacter fetus surface layer protein expression”
Molecular Microbiology- Volume 26 Issue 03 Page 433 - October 1997  
Molecular Microbiology- Volume 26 Issue 03 Page 433 - October 1997  
http://www.blackwell-synergy.com/doi/abs/10.1046/j.1365-2958.1997.6151958.x


6. PAUL EDMONDS, CHARLOTTE M. PATTON, TIMOTHY J. BARRETT, GEORGE K. MORRIS, ARNOLD G.STEIGERWALT, AND DON J. BRENNER
6. PAUL EDMONDS, CHARLOTTE M. PATTON, TIMOTHY J. BARRETT, GEORGE K. MORRIS, ARNOLD G.STEIGERWALT, AND DON J. BRENNER
“Biochemical and Genetic Characteristics of Atypical Campylobacter
“Biochemical and Genetic Characteristics of Atypical Campylobacter
fetus subsp. fetus Strains Isolated from Humans in the United States”
fetus subsp. fetus Strains Isolated from Humans in the United States”
JOURNAL OF CLINICAL MICROBIOLOGY, June 1985, p. 936-940 Vol. 21, No. 6
Journal of Clinical Microbiology, June 1985, p. 936-940 Vol. 21, No. 6
http://jcm.asm.org/cgi/reprint/21/6/936


7. NCBI –National center for biotechnology information
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=genome&cmd=Retrieve&dopt=Overview&list_uids=20090
8. E Wang, M M Garcia, M S Blake, Z Pei, and M J Blaser  “Shift in S-layer protein expression responsible for antigenic variation in Campylobacter fetus” Journal of bacteriology 1993 August; 175(16): 4979–4984.
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=204962
9. Dr. Stuart A. Thompson “Campylobacter Surface-Layers (S-Layers) and Immune Evasion”
Annals of Periodontology, December 2002, Vol. 7, No. 1, Pages 43-53
http://cat.inist.fr/?aModele=afficheN&cpsidt=14700417






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

Latest revision as of 15:14, 4 July 2011

This is a curated page. Report corrections to Microbewiki.

A Microbial Biorealm page on the genus Campylobacter fetus


Classification

Higher order taxa

Bacteria; Proteobacteria; Epsilon Proteobacteria; Campylobacterales; Campylobacteraceae; Campylobacter

Species

C. fetus


NCBI: Taxonomy

Description and significance

Campylobacter fetus is a slender, spirally curved bacterial pathogen, enclosed with an S layer of special crystalline surface proteins. (Their unique function will be discussed later) . It is a gram-negative species holding two membranes and a thin cell wall in between. It is a pathogen, and can reside anywhere in the human body. The Campylobacter fetus S layer proteins were found to have a virulence factor in resistance to the host immune defense mechanisms (5). According to the Journal of Clinical microbiology, (2) Two subspecies were then suspected to exist in the Campylobacter fetus. One was Campylobacter fetus subsp. fetus and Campylobacter fetus subsp. Venerealis. To further investigate the genetic diversity among C. fetus strains of different origins, multiple genetic analyses were used such as polymorphic DNA (RAPD), pulsed-field gel electrophoresis (PFGE), and DNA-DNA hybridization. (3) It was also mainly found that its natural habitat of C. fetus subsp. fetus is the intestinal tract of cattle, but it can also cause abortions.

Genome structure

Campylobacter fetus was completely sequenced and was found to have 1820 genes. It has a circular DNA. Its genome length is 1,773,615 nt. GC content is 33%, coding sequence is 90%.It as 3441 proteins(7).The two strains that were found were divided based on their lipopolysaccharide (LPS) composition. These unique strains must contain conserved sequences so to check their unique versus mutual sequences we used gel electrophoresis. This helped answer the unique method of this pathogen in changing its S layer proteins. A different study (5) reported the different multiple highly conserved S layer homologous proteins, that are tightly packed in this species. These special S layer proteins are of the sizes of 97-149 kDa. They attach to the N terminus of the cell wall lipopolysaccharide non covalently. The genome holds one promoter for these proteins; it has at least one open frame and a DNA inversion.

Cell structure and metabolism

It has flagella for motility using the proton motive force for energy. Since it is gram-negative, it has three layer of protection – inner membrane, thin murein layer and an outer membrane. This organism has the optimal growth at atmospheres enriched with CO2 and 5% oxygen with nitrogen or hydrogen according to the journal of bacteriology(2). Camplylobacter fetus needs an anaerobic environment for growth. It needs a respiratory type of metabolism for growth. These bacteria do not ferment; they also do not oxidize carbohydrates. Their entire energy is produced by certain amino acids and the tricarboxlic acid cycle intermediates. Their special features are their unique S layer surface proteins.

Ecology

Campylobacter fetus has been studied and shown to adhere to those intestinal epithelial cell lines that it invades in humans. The information from this study reported in the Canadian Journal of Microbiology (1) shows that this Campylobacter fetus showed capabilities of adhering to many cell lines. This is just one example of the kind of cells this bacterium interacts with. Since this is a pathogen it interacts with many host cells either in humans or in animals mostly cattle.

Pathology

Campylobacter fetus is a bacterium that can interact and disrupt reproduction cycles. Since they have many possible surface layer proteins they have an antigenic variation that can trick the immune system. There are two types of mechanism by which these bacteria infect since there are two subspecies. The Campylobacter fetus subsp. Venerealis is found on bull mucus layer over the crypt cell layer of the male prepuce. This way, the bacteria is transmitted to the female cattle and causes its infertility. This is also the way it will get transferred again during mating. Campylobacter fetus subsp. Fetus is using a different infection mechanism in which the animal whether bird, reptile ingest the bacteria, it invades the mucus cell and can cause an abortion. The two subspecies uses different ways to invade the host. Humans are mostly not affected but can accidentally ingest the Campylobacter fetus subsp. Fetus and suffer severe symptoms such as inflammation of intestinal tract.(5)

Application to Biotechnology

Not applicable for this species.

Current Research

  • Extensive research is being done through the years as well as in current times dealing with the big mystery of the S layer proteins that escape the immune system. Dr. Thompson (9)

Suggest two mechanisms for this. One is the resistance to the non-immune serum by preventing the binding of this serum to the C. fetus cell surface proteins. Another way might be the one I already mentioned about varying its S layer coat proteins thus avoid the antibodies of the immune system.

  • Another recent finding was made by Briedis (4) in which blood from a patient with cellulites showed evidence of C. fetus. Later on in testing, he found evidence for the other strain Venerealis. He continued with testing to show that the strains differ in their 1% glycine tolerance. More research was done by him to finalize the results and come with a more conclusive result as to what strain appeared in his patient.
  • To find more about the two different strains of Campylobacter fetus, Schulze (3) conducted some tests to examine the main differences between the two strains. He didn’t find more than what was already known of the two subspecies but ran results that gave more light for the main differences using some tests as PCR, temperature sensitivity, phenotype and genotype testing as well as many more.

References

1. Lori L Graham, “Campylobacter fetus adheres to and enters INT 407 cells” Canadian Journal of Microbiology 48 pp 995-1007 http://rparticle.web-p.cisti.nrc.ca/rparticle/AbstractTemplateServlet?journal=cjm&volume=48&year=&issue=&msno=w02-096&calyLang=fra

2. G M Carlone and J Lascelles, “Aerobic and anaerobic respiratory systems in Campylobacter fetus subsp. jejuni grown in atmospheres containing hydrogen” Journal of Bacteriology, 1982 October; 152(1): 306–314. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=221406

3. Frank Schulze, Audrey Bagon, Wolfgang Müller, and Helmut Hotzel, “Identification of Campylobacter fetus Subspecies by Phenotypic Differentiation and PCR” Journal of Clinical Microbiology 2006 June; 44(6): 2019–2024. http://jcm.asm.org/cgi/content/abstract/44/6/2019

4. Dalius J. Briedis, Ali Khamessan, Richard W. McLaughlin, Hojatollah Vali, Maria Panaritou, and Eddie C. S. Chan, “Isolation of Campylobacter fetus subsp. fetus from a Patient with Cellulitis” Journal of Clinical Microbiology, December 2002, p. 4792-4796, Vol. 40, No. 12 http://jcm.asm.org/cgi/content/full/40/12/4792

5. Joel Dworkin & Martin J. Blaser, “Molecular mechanisms of Campylobacter fetus surface layer protein expression” Molecular Microbiology- Volume 26 Issue 03 Page 433 - October 1997 http://www.blackwell-synergy.com/doi/abs/10.1046/j.1365-2958.1997.6151958.x

6. PAUL EDMONDS, CHARLOTTE M. PATTON, TIMOTHY J. BARRETT, GEORGE K. MORRIS, ARNOLD G.STEIGERWALT, AND DON J. BRENNER “Biochemical and Genetic Characteristics of Atypical Campylobacter fetus subsp. fetus Strains Isolated from Humans in the United States” Journal of Clinical Microbiology, June 1985, p. 936-940 Vol. 21, No. 6 http://jcm.asm.org/cgi/reprint/21/6/936

7. NCBI –National center for biotechnology information http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=genome&cmd=Retrieve&dopt=Overview&list_uids=20090

8. E Wang, M M Garcia, M S Blake, Z Pei, and M J Blaser “Shift in S-layer protein expression responsible for antigenic variation in Campylobacter fetus” Journal of bacteriology 1993 August; 175(16): 4979–4984. http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=204962

9. Dr. Stuart A. Thompson “Campylobacter Surface-Layers (S-Layers) and Immune Evasion” Annals of Periodontology, December 2002, Vol. 7, No. 1, Pages 43-53 http://cat.inist.fr/?aModele=afficheN&cpsidt=14700417


Edited by Sharon Porath of Rachel Larsen and Kit Pogliano