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AB252773

Anti-Clostridium difficile Toxin A antibody

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Goat Polyclonal Clostridium difficile Toxin A antibody.

View Alternative Names

toxA, tcdA, Toxin A

Key facts

Host species

Goat

Clonality

Polyclonal

Isotype

IgG

Carrier free

No

Applications

ELISA

applications

Reactivity data

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Properties and storage information

Form
Liquid
Purification technique
Affinity purification Immunogen
Storage buffer
Preservative: 0.1% Sodium azide Constituents: PBS
Shipped at conditions
Blue Ice
Appropriate short-term storage duration
1-2 weeks
Appropriate short-term storage conditions
+4°C
Appropriate long-term storage conditions
-20°C
Aliquoting information
Upon delivery aliquot
Storage information
Avoid freeze / thaw cycle

Supplementary information

This supplementary information is collated from multiple sources and compiled automatically.

Clostridium difficile Toxin A also known as C. diff toxin A or enterotoxin A acts mechanically by disrupting the cytoskeleton of intestinal epithelial cells. Weighing approximately 308 kDa this toxin gets expressed by Clostridium difficile bacteria during infection. C. diff toxin A enters the host cells inactivating Rho family GTPases leading to cell rounding and apoptosis. This disruption contributes to the weakening of the gut lining increasing its permeability.
Biological function summary

The main role of C. diff toxin A involves causing inflammation in the colonic mucosa. It functions as part of a dual toxin system with Toxin B. Toxin A binds to receptors on the surface of intestinal cells initiating a cascade that recruits neutrophils and other immune cells. This immune response exacerbates tissue damage and results in the observed symptoms of C. diff infections. The interaction with Toxin B enhances its pathogenic capacity further altering the tight junctions within the gut epithelium.

Pathways

C. diff toxin A affects the Rho-GTPase signaling pathway by acting as a glucosyltransferase and modifying small GTPases like Rho Rac and Cdc42. These changes impair the cell's cytoskeletal dynamics and disrupt cellular functions related to structural maintenance. Furthermore C. diff toxin A also influences the NF-kB pathway which plays a role in inflammation and immune responses. Toxin A's role in modifying these pathways highlights the coordinated interplay with Toxin B promoting inflammation and cytotoxicity.

The role of C. diff toxin A is prominent in Clostridium difficile infections (CDI) a significant cause of antibiotic-associated diarrhea and colitis. The presence of C. diff toxin A connects strongly to the severity of CDI leading to prolonged illness and complications like pseudomembranous colitis. Studies indicate an interaction with proteins like Toxin B that enhances the severity of infection and tissue destruction. Understanding C. diff toxin A's mechanisms can assist in developing therapeutic strategies targeting both toxins for effective treatment of CDI.

Product protocols

For this product, it's our understanding that no specific protocols are required. You can visit:

Target data

Toxin A. Precursor of a cytotoxin that targets and disrupts the colonic epithelium, inducing the host inflammatory and innate immune responses and resulting in diarrhea and pseudomembranous colitis (PubMed : 20844489). TcdA and TcdB constitute the main toxins that mediate the pathology of C.difficile infection, an opportunistic pathogen that colonizes the colon when the normal gut microbiome is disrupted (PubMed : 19252482, PubMed : 20844489). Compared to TcdB, TcdA is less virulent and less important for inducing the host inflammatory and innate immune responses (PubMed : 19252482). This form constitutes the precursor of the toxin : it enters into host cells and mediates autoprocessing to release the active toxin (Glucosyltransferase TcdA) into the host cytosol (By similarity). Targets colonic epithelia by binding to some receptor, and enters host cells via clathrin-mediated endocytosis (By similarity). Binding to LDLR, as well as carbohydrates and sulfated glycosaminoglycans on host cell surface contribute to entry into cells (PubMed : 16622409, PubMed : 1670930, PubMed : 31160825). In contrast to TcdB, Frizzled receptors FZD1, FZD2 and FZD7 do not act as host receptors in the colonic epithelium for TcdA (PubMed : 27680706). Once entered into host cells, acidification in the endosome promotes the membrane insertion of the translocation region and formation of a pore, leading to translocation of the GT44 and peptidase C80 domains across the endosomal membrane (By similarity). This activates the peptidase C80 domain and autocatalytic processing, releasing the N-terminal part (Glucosyltransferase TcdA), which constitutes the active part of the toxin, in the cytosol (PubMed : 17334356, PubMed : 19553670, PubMed : 27571750).. Glucosyltransferase TcdA. Active form of the toxin, which is released into the host cytosol following autoprocessing and inactivates small GTPases (PubMed : 22267739, PubMed : 22747490, PubMed : 24905543, PubMed : 30622517, PubMed : 7775453). Acts by mediating monoglucosylation of small GTPases of the Rho family (Rac1, RhoA, RhoB, RhoC, Rap2A and Cdc42) in host cells at the conserved threonine residue located in the switch I region ('Thr-37/35'), using UDP-alpha-D-glucose as the sugar donor (PubMed : 22267739, PubMed : 22747490, PubMed : 24905543, PubMed : 30622517, PubMed : 7775453). Monoglucosylation of host small GTPases completely prevents the recognition of the downstream effector, blocking the GTPases in their inactive form, leading to actin cytoskeleton disruption and cell death, resulting in the loss of colonic epithelial barrier function (PubMed : 7775453). Also able to catalyze monoglucosylation of some members of the Ras family (H-Ras/HRAS, K-Ras/KRAS and N-Ras/NRAS), but with much less efficiency than with Rho proteins, suggesting that it does not act on Ras proteins in vivo (PubMed : 30622517).
See full target information tcdA

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