The evolutionary success of parasitic worms causes significant economic losses and animal health problems, including in the small ruminant industry. The hematophagous nematode Haemonchus contortus is a common endoparasite that infects wild and domestic ruminants worldwide, especially in tropical and subtropical regions. To date, the most commonly applied control strategy is the administration of anthelminthic drugs. The main disadvantages of these chemicals are their ecotoxic effects, the necessary withdrawal period (especially important in dairy animals) and the increasing development of resistance. Vaccines offer an attractive alternative control strategy against Haemonchus infections. In previous years, several potential vaccine antigens prepared from H. contortus using the latest technologies have been assessed in clinical trials using different methods and strategies. This review highlights the current state of knowledge on anti-H. contortus vaccines (covering native, recombinant and DNA-based vaccines), including an evaluation, as well a discussion of the challenges and achievements in developing protective, efficient, and long-lasting vaccines to control H. contortus infection and haemonchosis in small ruminants. This paper also addresses novel developments tackling the challenge of glycosylation of putative candidates in recombinant form.
The H11 antigens, located on the intestinal microvilli of Haemonchus contortus , comprise a group of homologous aminopeptidases essential for the parasite’s digestion of blood meals. Native H11 proteins are promising vaccine antigens, capable of eliciting robust protective immunity against H. contortus in sheep and goats. However, recombinant forms of H11, produced either in conventional expression systems or in transgenic Caenorhabditis elegans , failed to replicate the protective efficacy of the native form, most likely due to two critical factors: improper glycosylation and protein misfolding. To address these limitations, we developed a novel strategy to produce recombinant Haemonchus antigens in glycoengineered insect cells. By introducing three C. elegans genes that alter the native N-glycosylation pathways of Hi5 insect cells we successfully expressed soluble H11 and GA1 antigens featuring nematode-specific glycan epitopes, including tri-fucosylated structures and the Galβ1,4Fuc motif. The glycoengineered H11 proteins retained aminopeptidase activity and stimulated cytokine secretion from ovine peripheral blood mononuclear cells in vitro . These findings establish a platform for producing bioactive vaccine antigens against the parasitic nematode H. contortus .
Haemonchus contortus is considered the most pathogenic nematode in small ruminants and South American camelids, causing significant production losses and threatening animal welfare worldwide. Compared to the use of anthelmintic drugs, to which resistance is increasing, vaccination is considered a more sustainable control strategy. The safety and efficacy of a novel glycoengineered vaccine produced in Hi5 insect cells was evaluated in a randomized, controlled vaccination-and-challenge trial. For this, 35 male Jura x Lacaune sheep were assigned to five groups (n=7). Three experimental groups were vaccinated three times subcutaneously with 1 ml of either the commercial Barbervax ® vaccine, the novel glycoengineered vaccine, consisting of a cocktail of five antigens (H11, H11-1, H11-2, H11-4 and GA1), or its non-glycoengineered counterpart before challenge with 5,000 H. contortus third-stage larvae. Clinical assessments, differential blood counts, serum antibody responses and fecal egg counts were evaluated at least once per week within the 16-week trial period. The abomasal worm burden was counted 40 days after challenge. The results of the mixed model showed a lower degree of anemia (mean packed cell volume (PCV) of 26.77%; mean hemoglobin (Hb) of 9.03 g/dl), in sheep vaccinated with the glycoengineered antigen cocktail compared to the unvaccinated group (PCV of 24.34%; mean Hb of 7.84 g/dl) and to the sheep vaccinated with the non-glycoengineered antigens (PCV of 26.11%; mean Hb of 8.53 g/dl). However, the degree of anemia was lower in sheep vaccinated with native antigens (Barbervax ® ) (PCV of 29.10%; mean Hb of 9.84 g/dl). Serum IgG and IgE antibodies were elevated in all vaccinated groups. Sheep vaccinated with the glycoengineered antigens showed a reduction in abomasal worm burden of 25.36% and a reduction of fecal egg shedding of 81.09%, the group vaccinated with non-glycoengineered antigen showed no worm reduction and a fecal egg count reduction of 32.72%. While there was no significant difference in egg shedding between sheep vaccinated with the glycoengineered antigens and sheep vaccinated with Barbervax ® (98.32%; p = 0.33), the Barbervax ® group showed a greater reduction in worm burden (86.40%). The results emphasize that glycoengineering of vaccine candidates is essential to achieve protective immunity against H. contortus in sheep and that the novel glycoengineered vaccine produced in insect cells clearly has the potential to reduce fecal egg shedding and worm burden, paving the way for the development of highly effective recombinant vaccines against this and other parasitic worms in the future.
Mycoplasma ovipneumoniae is an important respiratory pathogen in sheep, commonly implicated in chronic pneumonia. Although widely reported, data on its occurrence, strain diversity and the relationship between upper respiratory tract carriage and pulmonary infection remains limited. The study examined a conventional flock of 230 Merino x Berrichon du Cher ewes. Thirty-eight sheep underwent physical examination and nasal swabbing, including 15 animals with additional post-mortem lung sampling. Additionally, lungs from 15 further sheep were examined, yielding 30 lung samples for gross and histopathological assessment. Microbiological examination was performed using cultivation procedures and isolates were identified by applying MALDI-ToF mass spectrometry. Genetic diversity of M. ovipneumoniae strains was assessed using a newly established core genome MLST scheme. Clinical findings were consistent with respiratory disease, and lung lesions were compatible with M. ovipneumoniae-associated pneumonia. M. ovipneumoniae was cultivated from all 38 nasal swabs (100%) and from 27 of 30 lung samples (90%). Cultivation of lung samples identified three principal pathogens: M. ovipneumoniae, Pasteurella multocida, and Mannheimia haemolytica, with concurrent detection observed in a subset of cases. Core genome sequence-based typing indicated both high genetic diversity and the clonal spread of individual M. ovipneumoniae strains on the farm. This study documents M. ovipneumoniae infection in an Austrian sheep flock and highlights the frequent involvement of co-pathogens and the high genotypic diversity of circulating strains. These findings underscore the importance of targeted surveillance, molecular characterisation, and integrated control measures to mitigate respiratory disease. Further multi-farm and longitudinal studies are warranted to clarify transmission dynamics and the clinical significance of strain variation.