Ollscoil na Gaillimhe – University of Galway

education📍 Galway, Ireland
Ollscoil na Gaillimhe – University of Galway
3
Alpha-gal Syndrome Publications
3
Alpha-gal Syndrome Researchers

Associated Institutions

National University of Ireland
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University Hospital Galway
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Advanced Materials and BioEngineering Research
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Saolta University Health Care Group
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Irish Research eLibrary
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Publications

Differential alpha-gal expression during and tick feeding and development: A driver for the development of alpha-gal syndrome in South Africa.

Murangi T, Mans B, Pienaar R, Botha M, Facey-Thomas H, et al.
The journal of allergy and clinical immunology. Global •

The presence of galactose-α-1,3-galactose (alpha-gal) in tick salivary antigens has been implicated to initiate host IgE responses resulting in sensitization to alpha-gal. We sought to investigate the presence of alpha-gal in different anatomic locations in native South African tick species at different feeding and developmental stages and the ability of sera from our allergic cohort to bind to these tick proteins. Alpha-gal-containing proteins in laboratory-reared ticks at different feeding and developmental stages were detected through Western blotting and immunohistochemical staining. IgE and IgG4 toward the tick proteins were analyzed via ELISA. There is differential expression of alpha-gal in endemic South African ticks and . Immunoblotting demonstrated an increase in the prominence of alpha-gal-containing protein bands in salivary glands to be proportional to feeding time. Alpha-gal in both fed and unfed ticks was localized in the salivary acini and testes. IgE and IgG4 to antigens were significantly raised in alpha-gal-allergic individuals. There was a correlation between anti- IgE and anti-alpha-gal IgE in the alpha-gal-allergic group. Inhibition of human serum anti-alpha-gal IgE to and proteins was significantly reduced by the addition of bovine thyroglobulin. We anticipate repeated exposure to differentially expressed and alpha-gal-containing salivary proteins during feeding to cause alpha-gal sensitization.

Evaluation of lactoferrin administration as an antibiotic alternative growth promoter: impacts on rabbit's growth, meat quality, blood biochemical parameters, immune status, antioxidant status, and tissue histology.

Imbabi TA, Amer SA, Halawa EH, Sabeq II, Abdel-Warith AA, et al.
Tropical animal health and production •

Antibiotic-resistant microbes have emerged because of the widespread misuse of antibiotics in modern animal production. To overcome antibiotic resistance, the name lactoferrin (Lf) is promising since it is a naturally safe alternative to antibiotics. Considering the few sources available, this study evaluated the effects of Lf administration as a possible alternative to antibiotics on the growth, meat quality, blood hematology, hepato-renal function, antioxidant, and immune status of rabbits. A total of 60 four-week-old V-line male weaned rabbits (average body weight 530 ± 20 g) were randomly distributed to three experimental treatments (TRTs). The first TRT was the control group (CON). In the 2nd and 3rd TRTs, rabbits were orally administered with 1 mL oxytetracycline (OXY)/kg BW and 300 mg Lf/kg body weight (BW), respectively. The TRTs were applied orally twice weekly for 8 weeks. The results showed that the BW of rabbits treated with Lf was higher than the CON rabbits at the 8th and 12th week of age (P < 0.05). The average daily gain was higher in the Lf-treated group than in the CON and OXY-treated groups in the 12th week (P < 0.01). The meat quality parameters showed that Lf produced bright red meat with the highest lightness and lowest yellowness and hue values compared to OXY TRT and CON rabbits. At the same time, the other technological meat parameters, such as water holding capacity, drip loss (24 and 48 h), cooking loss, and Warner-Bratzler Shear Force, were not significantly changed. The serum levels of AST, ALT, ALP, and urea were reduced in the Lf-treated group and increased in the OXY-treated group compared with the CON. The total and direct bilirubin levels and creatinine and uric acid levels were increased in the OXY-treated rabbits. The total protein and globulin serum levels were raised in the Lf-treated rabbits and reduced in the OXY-treated rabbits. The albumin level decreased in the OXY-treated group. The serum levels of IgG and IgM were higher in the LF-treated animals compared to the CON and OXY-treated groups (P < 0.01). The serum levels of IgA, IgD, and IgE were increased in both Lf- and OXY-treated groups compared with the CON group. The hepatic and renal MDA and NO concentrations were decreased in the LF-treated group and increased in the OXY-treated group. The opposite is true for the activity of glutathione peroxidase, glutathione-reduced glutathione-S-transferase, and catalase. Lactoferrin administration upregulated the growth-related genes and downregulated the proinflammatory and apoptotic genes. In conclusion, lactoferrin in a dose of 300 mg /kg BW is a potential antibiotic alternative for improving rabbits' growth, health, meat quality, antioxidant, and immune status.

Ascaris lumbricoides and ticks associated with sensitization to galactose α1,3-galactose and elicitation of the alpha-gal syndrome.

Murangi T, Prakash P, Moreira BP, Basera W, Botha M, et al.
The Journal of allergy and clinical immunology •

IgE to galactose alpha-1,3 galactose (alpha-gal) causes alpha-gal syndrome (delayed anaphylaxis after ingestion of mammalian meat). Development of sensitization has been attributed to tick bites; however, the possible role of other parasites has not been well studied. Our aims were to assess the presence, relative abundances, and site of localization of alpha-gal-containing proteins in common ectoparasites and endoparasites endemic in an area of high prevalence of alpha-gal syndrome, as well as to investigate the ability of ascaris antigens to elicit a reaction in a humanized rat basophil in vitro sensitization model. Levels of total IgE, Ascaris-specific IgE, and alpha-gal IgE were measured in sera from patients with challenge-proven alpha-gal syndrome and from controls without allergy. The presence, concentration, and localization of alpha-gal in parasites were assessed by ELISA, Western blotting, and immunohistochemistry. The ability of Ascaris lumbricoides antigen to elicit IgE-dependent reactivity was demonstrated by using the RS-ATL8 basophil reporter system. Alpha-gal IgE level correlated with A lumbricoides-specific IgE level. Alpha-gal protein at 70 to 130 kDa was detected in A lumbricoides at concentrations higher than those found in Rhipicephalus evertsi and Amblyomma hebraeum ticks. Immunohistochemistry was used to localize alpha-gal in tick salivary acini and the helminth gut. Non-alpha-gal-containing A lumbricoides antigens activated RS-ATL8 basophils primed with serum from subjects with alpha-gal syndrome. We demonstrated the presence, relative abundances, and site of localization of alpha-gal-containing proteins in parasites. The activation of RS-ATL8 IgE reporter cells primed with serum from subjects with alpha-gal syndrome on exposure to non-alpha-gal-containing A lumbricoides proteins indicates a possible role of exposure to A lumbricoides in alpha-gal sensitization and clinical reactivity.