Bacterial Toxin Research Citations

RelA translocation assay:

OT-II CD90.1+CD4+ T cells were isolated from spleen and lymph nodes with a CD4+ T cell isolation kit (Miltenyi Biotec), and 0.51 3 106 cells were adoptively transferred into CD90.2+ wild-type recipients. The next day, recipient mice were injected i.v. with 5 mg of Escherichia coli LPS (List Biological Laboratories) diluted in PBS, and then a day later, some mice were injected i.v. with 100 mg of chicken OVA peptide 323339 (Invitrogen) diluted in PBS. …

Author did not specify which List Labs LPS product was utilized in their research.  List Labs provides the following LPS products:  https://listlabs.com/product-information/lipopolysaccharides/

EAE:

… on days 0 and 7 following Tompkins et al. (2002), with pertussis toxin (PTx) (List Biologicals) 200 ng ip on day 0 and day 2 and followed for evidence of disease. Clinical severity was graded daily as follows by a blinded … 

Author did not specify which List Labs Pertussis Toxin was utilized. List Labs provides the following Pertussis Toxin products:
• Product #180 – Pertussis Toxin from B. pertussis, Lyophilized in Buffer
• Product #181 – Pertussis Toxin from B. pertussis, Lyophilized (Salt-Free)
• Product #179A – Pertussis Toxin from B. pertussis (in Glycerol)

EAE Induction:

… On the day of immunization and again 2 d later, each mouse was injected ip with 200 ng pertussis toxin (List Biological Laboratories, Campbell, CA) in 0.1 ml PBS. Clinical EAE severity was …

Author did not specify which List Labs Pertussis Toxin was utilized. List Labs provides the following Pertussis Toxin products:
• Product #180 – Pertussis Toxin from B. pertussis, Lyophilized in Buffer
• Product #181 – Pertussis Toxin from B. pertussis, Lyophilized (Salt-Free)
• Product #179A – Pertussis Toxin from B. pertussis (in Glycerol)

Induction of active EAE:

EAE in male (8-to10-wk-old)mice was induced and evaluated as described previously (28). MOG3555 peptide was obtained from CPC Scientic (San Jose, CA) and pertussis toxin came from List Biological Laboratories (Campbell, CA).

Author did not specify which List Labs Pertussis Toxin was utilized. List Labs provides the following Pertussis Toxin products:
• Product #180 – Pertussis Toxin from B. pertussis, Lyophilized in Buffer
• Product #181 – Pertussis Toxin from B. pertussis, Lyophilized (Salt-Free)
• Product #179A – Pertussis Toxin from B. pertussis (in Glycerol)

… For active EAE induction, 200 ng pertussis toxin (List Biologicals, St. Louis, MO) was administered ip on days 0 and 2 to initiate disease. Animals were similarly immunized for passive EAE; 10 d later, the inguinal, brachial, and axillary LN were removed. …

Author did not specify which List Labs Pertussis Toxin was utilized. List Labs provides the following Pertussis Toxin products:
• Product #180 – Pertussis Toxin from B. pertussis, Lyophilized in Buffer
• Product #181 – Pertussis Toxin from B. pertussis, Lyophilized (Salt-Free)
• Product #179A – Pertussis Toxin from B. pertussis (in Glycerol)

… The LPS was purchased from a List Biological Lab (San Jose, CA, USA) …

Author did not specify which List Labs LPS product was utilized in their research.  List Labs provides the following LPS products:  https://listlabs.com/product-information/lipopolysaccharides/

Experimental Protocols:

Mice were treated with an intraperitoneal injection of 1 mg/kg purified LPS from E. coli 0111:B4 (List Biologicals) 4 hr prior to intravital microscopy. The dose of LPS used in this study was sufficiently low that animals survived anesthesia and hepatic perfusion was not severely diminished. The purity of the commercial LPS was confirmed by inoculation into TLR4 knockout (TLR4^/) animals and observation of no measurable response in any of the parameters reported in this study (data not shown). For platelet depletion experiments, mice were injected i.p. with 50 l anti-mouse thrombocyte serum or 50 l control serum (adsorbed normal rabbit serum) 24 hr prior to LPS administration or E. coli infection. For neutrophil depletion experiments, mice were injected i.p. with 200 g anti-Gr-1 antibody or 200 g rat IgG control antibody 24 hr prior to LPS administration. Platelet and neutrophil depletion were confirmed with SD-IVM (see Figure 2). In some experiments, mice were treated with 2000 U DNase intravenously at various time points after infection with E. coli (noted in the figure legends). 

• Product #201 – LPS from Escherichia coli O111:B4

Mouse Treatments and Immunizations:

For immunization with OVA in complete Freunds adjuvant (OVA/CFA), OVA was emulsified in CFA at final concentration of 1 mg/ml OVA, and mice received hind footpad injection of 20 l of OVA/CFA as described (Webster et al., 2006).

Foxp3-DTR mice express simian diphtheria toxin (DT) receptor that allows for depletion of Foxp3⁺ regulatory T cells upon DT administration (Kim et al., 2007; Chinen et al., 2010). For regulatory T cell depletion, wild-type control or Foxp3-DTR mice were injected intraperitoneally with 1.5 g of DT … List Biological Laboratory, Campbell, CA, USA) on days 0, 1, 4, and 7 and examined on day 8. CD4⁺, CD25⁺, Foxp3⁺ regulatory T cells in lymph nodes were depleted by at least 12-fold by day 8.

• Product #150 – Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

… Frozen sections of the brain, the TG, and the eye muscles were processed for the immunocytochemical detection of the tracers cholera toxin subunit B and wheat germ agglutinin (goat anti-choleragenoid, 1:5000; List Biological Laboratories, Campbell, CA, USA; …

• Product #703 – Anti-Cholera Toxin B Subunit (Goat)

Muscle afferent tracing:

Three days after PTx injury, animals were reanesthetized and muscle afferents of the deep radial nerve were labeled with 10 µl injections of a 1% solution of cholera toxin B (CTB) (List Biological Laboratories) into the extensor carpi radialis of both forelimbs. The solution was injected over 1 min, and the needle was withdrawn over an additional 1 min. The wound was closed by suturing the overlying muscle and skin. Preliminary data demonstrated that CTB transganglionically labeled both primary sensory afferents and retrogradely labeled motoneuron pools. Anterograde labeling is punctate. Whereas at high magnification we could see punctate ventral horn labeling in proximity to labeled motoneurons, we were not able to distinguish this labeling from other ventral horn label, including portions of motoneuron dendrites and labeled recurrent motoneuron axon collaterals. For this reason, we limited our quantitative CTB analysis to the dorsal horn and intermediate zone. To assay putative 1A boutons on motoneuron cell bodies and proximal dendrites, we examined VgluT1 presynaptic labeling. …

• Product #104 – Cholera Toxin B Subunit (Choleragenoid) from Vibrio cholerae in Low Salt