Mycoplasma penetrans

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Mycoplasma penetrans
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Bacteria
Phylum: Mycoplasmatota
Class: Mollicutes
Order: Mycoplasmatales
Family: Mycoplasmataceae
Genus: Mycoplasma
Species:
M. penetrans
Binomial name
Mycoplasma penetrans
Lo et al. 1992

Mycoplasma penetrans is a species of Gram-positive bacteria. [1] [2] It is pathogenic, though many infected show no symptoms. It is a sexually transmitted disease, though an infant may be infected during birth. [3] [4]

Contents

Description

It has an elongated shape and its cells possess two internal compartments, one packed with granules, the other filled with coarse granules (consistent with ribosomal structures). The organism has properties of adherence through a specific organelle called the tip organelle. M. Penetrans has a coding sequence (MYPE1570) similar to that of MYPE470 in Mycoplasma pneumoniae which codes for an accessory protein that aids in cytadherence, [5] the adherence to respiratory epithelium. This similarity suggests M. penetrans could attach to host cells through cytadherence. Also, the CDS MYPE1550, which is near MYPE1570, of M. penetrans is orthologous to the hemadsorption protein HMW2 of M pneumoniae, suggesting the potential for M. penetrans to attach to and invade red blood cells. [5]

Virulence factors

Mycoplasma penetrans, like many bacteria, exhibits a mechanism by which it can avoid an immune response in the host cells. This avoidance of immune responses is known as a virulence factor. The virulence factor that M. penetrans displays is antigenic variation, the ability to exchange or switch antigens against which the host cell produces antibodies. The mpl gene encodes for the bacteria's antigens and, like most genes, it contains a promoter region. In M. penetrans, this promoter region can undergo reversible inversion, allowing for variation in antigen production and, thus, the source for M. penetrans antigenic variation. [6]

Diseases

Mycoplasma penetrans has been shown to hinder p53, a tumor suppressing gene that aids in regulating the cell cycle. [7] There have also been cases of malignant pleural effusion, when patients exhibited chronic M. penetrans infection with various immunodeficiencies (such as HIV infections or anticancer treatment). [8] This particular species is also a sexually transmitted disease and one cause of pelvic inflammatory disease. [9]

Related Research Articles

<span class="mw-page-title-main">Mycoplasma genitalium</span> Species of bacterium

Mycoplasma genitalium is a sexually transmitted, small and pathogenic bacterium that lives on the mucous epithelial cells of the urinary and genital tracts in humans. Medical reports published in 2007 and 2015 state that Mgen is becoming increasingly common. Resistance to multiple antibiotics, including the macrolide azithromycin, which until recently was the most reliable treatment, is becoming prevalent. The bacteria was first isolated from the urogenital tract of humans in 1981, and was eventually identified as a new species of Mycoplasma in 1983. It can cause negative health effects in men and women. It also increases the risk factor for HIV spread with higher occurrences in those previously treated with the azithromycin antibiotics.

<i>Yersinia pestis</i> Species of bacteria, cause of plague

Yersinia pestis is a gram-negative, non-motile, coccobacillus bacterium without spores that is related to both Yersinia enterocolitica and Yersinia pseudotuberculosis, the pathogen from which Y. pestis evolved and responsible for the Far East scarlet-like fever. It is a facultative anaerobic organism that can infect humans via the Oriental rat flea. It causes the disease plague, which caused the Plague of Justinian and the Black Death, the deadliest pandemic in recorded history. Plague takes three main forms: pneumonic, septicemic, and bubonic. Yersinia pestis is a parasite of its host, the rat flea, which is also a parasite of rats, hence Y. pestis is a hyperparasite.

<span class="mw-page-title-main">Biofilm</span> Aggregation of bacteria or cells on a surface

A biofilm is a syntrophic community of microorganisms in which cells stick to each other and often also to a surface. These adherent cells become embedded within a slimy extracellular matrix that is composed of extracellular polymeric substances (EPSs). The cells within the biofilm produce the EPS components, which are typically a polymeric combination of extracellular polysaccharides, proteins, lipids and DNA. Because they have a three-dimensional structure and represent a community lifestyle for microorganisms, they have been metaphorically described as "cities for microbes".

<i>Mycoplasma</i> Genus of bacteria

Mycoplasma is a genus of bacteria that, like the other members of the class Mollicutes, lack a cell wall, and its peptidoglycan, around their cell membrane. The absence of peptidoglycan makes them naturally resistant to antibiotics such as the beta-lactam antibiotics that target cell wall synthesis. They can be parasitic or saprotrophic. Several species are pathogenic in humans, including M. pneumoniae, which is an important cause of "walking" pneumonia and other respiratory disorders, and M. genitalium, which is believed to be involved in pelvic inflammatory diseases. Mycoplasma species are among the smallest organisms yet discovered, can survive without oxygen, and come in various shapes. For example, M. genitalium is flask-shaped, while M. pneumoniae is more elongated, many Mycoplasma species are coccoid. Hundreds of Mycoplasma species infect animals.

Mycoplasma hominis is a species of bacteria in the genus Mycoplasma. M. hominis has the ability to penetrate the interior of human cells. Along with ureaplasmas, mycoplasmas are the smallest free-living organisms known.

Mycoplasma pneumoniae is a very small cell wall-less bacterium in the class Mollicutes. It is a human pathogen that causes the disease mycoplasma pneumonia, a form of atypical bacterial pneumonia related to cold agglutinin disease. M. pneumoniae is characterized by the absence of a peptidoglycan cell wall and resulting resistance to many antibacterial agents. The persistence of M. pneumoniae infections even after treatment is associated with its ability to mimic host cell surface composition.

The periplasm is a concentrated gel-like matrix in the space between the inner cytoplasmic membrane and the bacterial outer membrane called the periplasmic space in gram-negative bacteria. Using cryo-electron microscopy it has been found that a much smaller periplasmic space is also present in gram-positive bacteria, between cell wall and the plasma membrane. The periplasm may constitute up to 40% of the total cell volume of gram-negative bacteria, but is a much smaller percentage in gram-positive bacteria.

<i>Ureaplasma urealyticum</i> Species of bacterium

Ureaplasma urealyticum is a bacterium belonging to the genus Ureaplasma and the family Mycoplasmataceae in the order Mycoplasmatales. This family consists of the genera Mycoplasma and Ureaplasma. Its type strain is T960. There are two known biovars of this species; T960 and 27. These strains of bacteria are commonly found as commensals in the urogenital tracts of human beings, but overgrowth can lead to infections that cause the patient discomfort. Unlike most bacteria, Ureaplasma urealyticum lacks a cell wall making it unique in physiology and medical treatment.

Mycoplasma pneumonia is a form of bacterial pneumonia caused by the bacterium Mycoplasma pneumoniae.

<span class="mw-page-title-main">Mycoplasmataceae</span> Family of bacteria

Mycoplasmataceae is a family of bacteria in the order Mycoplasmatales. This family consists of the genera Mycoplasma and Ureaplasma.

<i>Shigella flexneri</i> Species of bacterium

Shigella flexneri is a species of Gram-negative bacteria in the genus Shigella that can cause diarrhea in humans. Several different serogroups of Shigella are described; S. flexneri belongs to group B. S. flexneri infections can usually be treated with antibiotics, although some strains have become resistant. Less severe cases are not usually treated because they become more resistant in the future. Shigella are closely related to Escherichia coli, but can be differentiated from E.coli based on pathogenicity, physiology and serology.

<span class="mw-page-title-main">Endometritis</span> Medical condition

Endometritis is inflammation of the inner lining of the uterus (endometrium). Symptoms may include fever, lower abdominal pain, and abnormal vaginal bleeding or discharge. It is the most common cause of infection after childbirth. It is also part of spectrum of diseases that make up pelvic inflammatory disease.

Antigenic variation or antigenic alteration refers to the mechanism by which an infectious agent such as a protozoan, bacterium or virus alters the proteins or carbohydrates on its surface and thus avoids a host immune response, making it one of the mechanisms of antigenic escape. It is related to phase variation. Antigenic variation not only enables the pathogen to avoid the immune response in its current host, but also allows re-infection of previously infected hosts. Immunity to re-infection is based on recognition of the antigens carried by the pathogen, which are "remembered" by the acquired immune response. If the pathogen's dominant antigen can be altered, the pathogen can then evade the host's acquired immune system. Antigenic variation can occur by altering a variety of surface molecules including proteins and carbohydrates. Antigenic variation can result from gene conversion, site-specific DNA inversions, hypermutation, or recombination of sequence cassettes. The result is that even a clonal population of pathogens expresses a heterogeneous phenotype. Many of the proteins known to show antigenic or phase variation are related to virulence.

<span class="mw-page-title-main">Pathogenic bacteria</span> Disease-causing bacteria

Pathogenic bacteria are bacteria that can cause disease. This article focuses on the bacteria that are pathogenic to humans. Most species of bacteria are harmless and are often beneficial but others can cause infectious diseases. The number of these pathogenic species in humans is estimated to be fewer than a hundred. By contrast, several thousand species are part of the gut flora present in the digestive tract.

<span class="mw-page-title-main">Cyclic di-AMP</span> Chemical compound

Cyclic di-AMP is a second messenger used in signal transduction in bacteria and archaea. It is present in many Gram-positive bacteria, some Gram-negative species, and archaea of the phylum Euryarchaeota.

<span class="mw-page-title-main">Tubal factor infertility</span> Medical condition

Tubal factor infertility (TFI) is female infertility caused by diseases, obstructions, damage, scarring, congenital malformations or other factors which impede the descent of a fertilized or unfertilized ovum into the uterus through the fallopian tubes and prevents a normal pregnancy and full term birth. Tubal factors cause 25-30% of infertility cases. Tubal factor is one complication of chlamydia trachomatis infection in women.

The vaginal flora in pregnancy, or vaginal microbiota in pregnancy, is different from the vaginal flora before sexual maturity, during reproductive years, and after menopause. A description of the vaginal flora of pregnant women who are immunocompromised is not covered in this article. The composition of the vaginal flora significantly differs in pregnancy. Bacteria or viruses that are infectious most often have no symptoms.

Chlamydia research is the systematic study of the organisms in the taxonomic group of bacteria Chlamydiota, the diagnostic procedures to treat infections, the disease chlamydia, infections caused by the organisms, the epidemiology of infection and the development of vaccines. The process of research can include the participation of many researchers who work in collaboration from separate organizations, governmental entities and universities.

References

  1. Gallego, Pablo; Planell, Raquel; Benach, Jordi; Querol, Enrique; Perez-Pons, Joseph A.; Reverter, David (October 17, 2012). "Structural Characterization of the Enzymes Composing the Arginine Deiminase Pathway in Mycoplasma penetrans". PLOS ONE. 7 (10): e47886. Bibcode:2012PLoSO...747886G. doi: 10.1371/journal.pone.0047886 . PMC   3474736 . PMID   23082227 . Retrieved 11 November 2014.
  2. Lo, S.-C.; Hayes, M. M.; Tully, J. G.; Wang, R. Y.-H.; Kotani, H.; Pierce, P. F.; Rose, D. L.; Shih, J. W.-K. (1992). "Mycoplasma penetrans sp. nov., from the Urogenital Tract of Patients with AIDS". International Journal of Systematic Bacteriology. 42 (3): 357–364. doi: 10.1099/00207713-42-3-357 . ISSN   0020-7713. PMID   1503969.
  3. Yáñez A, Cedillo L, Neyrolles O, et al. (1999). "Mycoplasma penetrans bacteremia and primary antiphospholipid syndrome". Emerging Infectious Diseases . 5 (1): 164–7. doi:10.3201/eid0501.990122. PMC   2627698 . PMID   10081687.
  4. Ljubin-Sternak, Sunčanica; Meštrović, Tomislav (2014). "Chlamydia trachomatis and Genital Mycoplasmas: Pathogens with an Impact on Human Reproductive Healthogens with an Impact on Human Reproductive Health". Journal of Pathogens. 2014: 183167. doi: 10.1155/2014/183167 . PMC   4295611 . PMID   25614838.
  5. 1 2 Sasaki, Y.; Ishikawa, J.; Yamashita, A.; Oshima, K.; Kenri, T.; Furuya, K.; Hattori, M (2002-12-01). "The complete genomic sequence of Mycoplasma penetrans, an intracellular bacterial pathogen in humans". Nucleic Acids Research. 30 (23): 5293–5300. doi:10.1093/nar/gkf667. ISSN   1362-4962. PMC   137978 . PMID   12466555.
  6. Horino, A.; Sasaki, Y.; Sasaki, T.; Kenri, T. (2003-01-01). "Multiple Promoter Inversions Generate Surface Antigenic Variation in Mycoplasma penetrans". Journal of Bacteriology. 185 (1): 231–242. doi:10.1128/jb.185.1.231-242.2003. ISSN   0021-9193. PMC   141813 . PMID   12486060.
  7. Logunov, D Y; Scheblyakov, D V; Zubkova, O V; Shmarov, M M; Rakovskaya, I V; Gurova, K V; Tararova, N D; Burdelya, L G; Naroditsky, B S (2008-04-14). "Mycoplasma infection suppresses p53, activates NF-κB and cooperates with oncogenic Ras in rodent fibroblast transformation". Oncogene. 27 (33): 4521–4531. doi:10.1038/onc.2008.103. ISSN   0950-9232. PMC   4526267 . PMID   18408766.
  8. Cao, Shuyan; Shen, Dandan; Wang, Yadong; Li, Linxi; Zhou, Liping; Wang, Yuxue (2017-07-10). "Potential malignant transformation in the gastric mucosa of immunodeficient mice with persistent Mycoplasma penetrans infection". PLOS ONE. 12 (7): e0180514. Bibcode:2017PLoSO..1280514C. doi: 10.1371/journal.pone.0180514 . ISSN   1932-6203. PMC   5503272 . PMID   28692662. (Retracted, see doi:10.1371/journal.pone.0241463, PMID   33091082 . If this is an intentional citation to a retracted paper, please replace {{ retracted |...}} with {{ retracted |...|intentional=yes}}.)
  9. Ljubin-Sternak, Suncanica; Mestrovic, Tomislav (2014). "Review: Chlamydia trachonmatis and Genital Mycoplasmias: Pathogens with an Impact on Human Reproductive Health". Journal of Pathogens. 2014 (183167): 183167. doi: 10.1155/2014/183167 . PMC   4295611 . PMID   25614838.

Further reading