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Abstract Parasitism rates and parasitoid development can be influenced by the species and developmental stage of the host, both of these factors can influence parasitoid performance and fitness. In this study, parasitism rates and developmental parameters were assessed for two widely distributed and commercially available species of aphid parasitoid: Aphidius ervi (Hymenoptera: Braconidae) and Aphelinus abdominalis (Hymenoptera: Aphelinidae). In a first bioassay, parasitism rates and parasitoid development were investigated in different host species. The wasp A. ervi was tested on Macrosiphum euphorbiae, Rhopalosiphum padi, and Myzus persicae (Hemiptera: Aphididae) and A. abdominalis was tested on M. persicae, R. padi, and Rhopalosiphum maidis (Hemiptera: Aphididae). The results indicated that A. ervi had a greater percentage of emergence, higher percentage of parasitized aphids, longer developmental time, and higher proportion of females in M. persicae than in the other hosts. A. abdominalis had a greater percentage of emergence, larger progeny, and shorter developmental time in R. padi than in the other hosts. A second bioassay evaluated the preference of the parasitoids for different instars of their respective optimum host aphids in terms of parasitism and development, as determined in the first bioassay. The results showed that A. ervi produced a greater number of mummies in the fourth instar and in adults of M. persicae. In contrast, A. abdominalis preferred the first instar of R. padi. In conclusion, our results indicate that both parasitoid species exhibit different parasitism parameters depending upon the host species and the host stage. This suggests that these parasitoid species could be potentially complementary on multiple or combined releases of biological control programs.

Mast cells in the left cranial pulmonary lobe of colostrum-deprived neonatal calves were quantified 2 and 6 h after intrabronchial inoculation with Mannheimia (Pasteurella) haemolyticaA1. The mast cells were detected (1) immunohistochemically with a mouse anti-human mast cell tryptase monoclonal antibody, and (2) by metachromatic staining with low pH toluidine blue. A greater number of mast cells was demonstrated by the second method than by the first. At 6 h after inoculation, but not at 2 h, the number of mast cells was significantly reduced at the site of the main lesions. Treatment of calves with a sialyl Lewis mimetic (TBC1269) did not appreciably affect the results at 6 h.

Immune complex formation has long been thought to play a role in the pathogenesis of Pasteurella haemolytica pneumonia. This study in laboratory rabbits was designed to investigate immune-mediated damage in respiratory tissue caused by lipopolysaccharide (LPS). Severe lesions were induced by the intratracheal (IT) injection of P. haemolytica A1 LPS (50 @mg) into rabbits previously immunized with P. haemolytica killed whole cells emulsified with Freund's incomplete adjuvant (FIA); these lesions included perivascular oedema and polymorphonuclear leucocyte (PMN) infiltration of the subintima, with degeneration and necrosis of the media. Smaller vessels were occluded by PMNs in various stages of degranulation. PMN counts in bronchoalveolar lavage (BAL) fluid were significantly elevated (P<0.05). Lesions were also induced by the IT injection of LPS (50@mg) into rabbits pretreated with an emulsion consisting merely of FIA and formol-saline; these lesions included moderate to severe congestion, interstitial oedema, alveolar serofibrinous exudation and PMN infiltration. PMNs were also present in BAL fluid. Rabbits pretreated with FIA in formol-saline and given a later IT injection of saline, and rabbits pretreated with bovine serum albumin (BSA) in FIA and given a later IT injection of BSA, were included as negative and positive control groups. Cutaneous lesions were also induced by the intradermal injection of LPS into rabbits immunized against P. haemolytica and of BSA into rabbits immunized with BSA. Overall, the pulmonary and cutaneous lesions induced in vaccinated rabbits by antigen administration were more severe than those seen in non-vaccinated rabbits. The lesions in rabbits, which were similar to those seen in natural cases of P. haemolytica pneumonia in cattle, were characterized by a fibrinopurulent inflammatory process with extensive interstitial oedema, fibrinous exudate, and PMNs. This model may help to elucidate the pathogenesis of pneumonic pasteurellosis in immunized animals.