Breeding for immune responsiveness and disease resistance1

Animal production efficiency, and product volume and quality can be greatly increased by reducing disease losses. Genetic variation, a prerequisite for successful selection, has been found in animals and poultry exposed to a variety of viral, bacterial and parasitic infections. Breeding for disease resistance can play a significant role alone or in combination with other control measures including disease eradication, vaccination and medication. Feasibility of simultaneously improving resistance to specific diseases and production traits has been demonstrated. However, selection for specific resistance to all diseases of animals and poultry is impossible. Development of general disease resistance through indirect selection primarily on immune response traits may be the best long-term strategy but its applicability is presently limited by insufficient understanding of resistance mechanisms. Another hindrance may be negative genetic correlations among various immune response functions: phagocytosis, cell mediated and humoral immunity. To better assess the feasibility of increasing general disease resistance by indirect selection we must obtain estimates of heritability for immune response, disease resistance, and economic production traits, as well as genetic correlations among these traits. The present level of disease resistance in farm animals resulted from natural selection and from correlated responses to selection for production traits while the influence of artificial selection for resistance was minimal. Future research should be directed towards developing and applying breeding techniques that will increase resistance to diseases without compromising production efficiency and product quailty. This will require cooperation of immunogeneticists, veterinarians and animal and poultry breeders. Significant progress in the improvement of resistance to diseases may result from the application of new techniques of molecular genetics and cell manipulation.     

Breeding for resistance to whitefly-transmitted geminiviruses

Geminiviruses comprise a large and diverse family of viruses that infect a wide range of important monocotyledonous and dicotyledonous crop species and cause significant yield losses. The family Geminiviridae is divided into three genera, one of which is Begomovirus. Species of this genus are transmitted by the whitefly Bemisia tabaci in a persistent, circulative manner and infect dicotyledonous plants. Severe population outbreaks of B. tabaci are usually accompanied by a high incidence of begomoviruses. During the last two decades, there has been a worldwide spread of the B biotype of B. tabaci, accompanied by the emergence of whitefly‐transmitted geminiviruses. Control measures in infected regions are based mainly on limitation of vector populations, using chemicals or physical barriers. However, under conditions of severe whitefly attack, none of these control measures has sufficed to prevent virus spread. Thus, the best way to reduce geminivirus damage is by breeding crops resistant or tolerant to the virus, either by classical breeding or by genetic engineering. A number of begomoviruses have been the subject of much investigation, due to their severe economic impact. This review considers the most severe viral diseases of four major crops (tomato, bean, cassava and cotton). The approaches taken to breed for resistance to these viral diseases should provide a perspective of the issues involved in breeding for begomovirus resistance in crop plants.     

Phylogeny of immune responsiveness in invertebrates

Existence of essential immunocompetence at different levels of complexity has recently been demostrated among diverse phylums of invertebrates. $\text{Immunorecognition}$ or capacity for non-self recognition of allogeneic tissue followed by incompatibility reactions is already found in Coelenterates as shown in colonial hydroids, gorgonians, and hard corals. Antagonistic reactions reveal convincing specificity, with compatible fusion preceding manifestations of incompatibility, but no memory component has been demonstrated. Allogeneic contact incompatibilities found in protochordates as well as mixed lymphocyte culture reactions between allogeneic cells of various vertebrates may tentatively be assigned to this “sipmle” immunorecognition category. $\text{Primordial Cell-Mediated Immunity}$ (PCMI) represents a higher level of immunoevolution revealed by specific allograft reactions with at least short-term memory as found in Annelids and Echinoderms. PCMI is inherent in populations of leukocytes and definitely has an immune memory component. $\text{Integrated Cell-Mediated and Humoral Antibody Immunity}$ may be regarded as the highest level of immunoevolution characteristic of all vertebrates from primitive fishes to mammals. Vertebrate-type immunoglobulin antibodies have yet to be demonstrated in any invertebrate species, although cell-surface receptors akin to antibodies are apparent on leukocytes of advanced invertebrates. The less elaborate immunoresponsiveness evident among invertebrates awaits definitive characterization.     

Parasite survival and variability in host immune responsiveness

Immune responses are considered to play an important role in the regulation of parasite populations, by virtue of their influences upon the establishment, development, survival and reproduction of parasites in individual hosts. The capacity of hosts to generate and express effective responses is genetically determined and, therefore, variable in a genetically heterogeneous population. Survival of parasites is enhanced when the host's capacity is reduced or absent. Low- or non-responder hosts may play an important part in maintaining parasite population levels. Data derived from field or experimental studies of infections in small mammals are used to illustrate the relationships between genetics, immunity and parasite survival.     

Breeding for digenic apple resistance to scab

The results of the apple breeding for digenic resistance to scab (1979-2000), which is more long-term than the monogenic breeding, have been reviewed. The hybrid seeds obtained from the reciprocal crossing between the Vf and Vm resistance gene donors served as the original material. The seed progeny yielded by backcrosses between these hybrids and the susceptible cultivars were examined (age--first true leaves) using inoculation in a greenhouse. The following criteria were proposed for breeding parental forms and the cultivars of the VfvfVmvm genotype: (1) phenotype segregation in the progeny of three resistant: one susceptible seedling and (2) the presence in the progeny of two types of resistant seedlings: those with the class 1 resistance (points and spots-hypersensitivity) typical of the Vm gene and those with the class 2-3 resistance (chlorotic and necrotic spots) typical of the Vf gene.     

Breeding for resistance to diseases in greengram and blackgram

Summary This review is given on the origin and interrelationship of blackgram and greengram: the symptoms, mode of transmission, and host range of important diseases, namely: mungbean yellow mosaic virus, leaf crinkle virus, leaf curl virus, mosaic mottle virus, Cercospora leaf spot, powdery mildew, root and stem rots, bacterial leaf spot and halo blight. The screening for resistance, sources of resistance, including interspecific hybridization, and induced mutations, as well as the genetics of resistance are treated along with suggestions for future breeding strategies of these crops.Greengram is relatively drought tolerant. It is cultivated in India, Pakistan, Bangladesh, Srilanka, Thailand, Laos, Kampuchea, Vietnam, eastern Malaysia, Southern China and in the relatively dry eastern parts of Java, (Jain and Mehra 1978). In the recent past it has been introduced into the eastern and central parts of Africa, the West Indies and the U.S.A. It is also grown in the Philippines, Nepal, Taiwan and Indonesia. Blackgram has greater water requirements than greengram. It is grown in India, Pakistan, Srilanka and Burma (Jain and Mehra 1978).     

Breeding cattle and sheep for resistance to gastrointestinal nematodes

Gastrointestinal nematodes are an important cause of reduced production of meat, milk and wool in domestic livestock. It is generally believed that problems caused by these parasites have increased owing to the intensification of animal husbandry(1-3) of resistance to anthelmintics, current research is focussed on alternative control strategies that do not rely on anthelmintics. Here, Bram Kloosterman, Henk Parmentier and Harm Ploeger review work on the genetic resistance of domestic ruminants to these nematodes and discuss the practicality of breeding programmes.     

Antigen-induced in vitro inhibition of immune responsiveness

Addition of the dinitrophenyl derivative of the copolymer of d-glutamic acid and d-lysine (DNP-d-GL) or dinitrophenyl bovine γ-globulin (DNP-BGG) to spleen cell cultures specifically inhibited their capacity to produce an anti-DNP plaque-forming cell (PFC) response to the T-independent antigen dinitrophenylated polyacrylamide beads (DNP-PAA) or to the T-dependent antigen TNP-burro erythrocytes. The degree of unresponsiveness was dependent upon the tolerogen concentration and the duration over which the tolerogen was present in the culture. Treatment with rabbit anti-mouse brain antiserum and complement did not alter the induction of unresponsiveness suggesting a state of B-cell tolerance. Culture of spleen cells for 4 days in the absence of antigen led to the appearance of nonspecific suppressor activity which was demonstrable by its effect on the response of fresh spleen cells to antigen. Preculture in the presence of the immunogen DNP-PAA induced both nonspecific and specific suppressor activities. Induction of specific suppressor activity was not prevented by the presence of the tolerogen DNP-D-GL in the culture. The suppressor activity resided in an adherent T-cell population and did not appear to require macrophages for its induction.     

Breeding for resistance to aflatoxin accumulation in maize

Contamination of maize,Zea mays, grain with aflatoxin, a naturally occurring toxin produced byAspergillus flavus, frequently reduces the value and marketability of maize produced in the southern USA. Drought, high temperatures, and insect damage are often associated with high levels of maize aflatoxin contamination. Growing resistant maize hybrids is generally considered the most feasible method of reducing or eliminatingA. flavus infection and subsequent accumulation of aflatoxin. Developing appropriate screening techniques and identifying maize germplasm with resistance to aflatoxin contamination provides the foundation for a breeding program. Only a few sources of aflatoxin resistance have been identified. Four germplasm lines (Mp313E, Mp420, Mp715, and Mp717) have been developed and released by USDA-ARS at Mississippi State University. NC 388, developed at North Carolina State University, is reported as another putative source of aflatoxin resistance. Conventional phenotypic selection was used to successfully combine resistance to aflatoxin contamination from two of these lines, Mp313E and Mp715, with desirable agronomic qualities from Va35. The identification of quantitative trait loci (QTL) associated with resistance to aflatoxin contamination will also permit the use of marker assisted selection in transferring resistance into elite germplasm lines. Development of parental inbreds that combine aflatoxin resistance with superior agronomic quality is an essential component of a hybrid maize breeding program designed to reduce or eliminate aflatoxin contamination.     

Apoptosis and other immune biomarkers predict influenza vaccine responsiveness

Despite the importance of the immune system in many diseases, there are currently no objective benchmarks of immunological health. In an effort to identifying such markers, we used influenza vaccination in 30 young (20–30 years) and 59 older subjects (60 to >89 years) as models for strong and weak immune responses, respectively, and assayed their serological responses to influenza strains as well as a wide variety of other parameters, including gene expression, antibodies to hemagglutinin peptides, serum cytokines, cell subset phenotypes and in vitro cytokine stimulation. Using machine learning, we identified nine variables that predict the antibody response with 84% accuracy. Two of these variables are involved in apoptosis, which positively associated with the response to vaccination and was confirmed to be a contributor to vaccine responsiveness in mice. The identification of these biomarkers provides new insights into what immune features may be most important for immune health.     

Adverse environmental conditions influence age-related innate immune responsiveness

Background-  

The innate immune system plays an important role in the recognition and induction of protective responses against infectious pathogens, whilst there is increasing evidence for a role in mediating chronic inflammatory diseases at older age. Despite indications that environmental conditions can influence the senescence process of the adaptive immune system, it is not known whether the same holds true for the innate immune system. Therefore we studied whether age-related innate immune responses are similar or differ between populations living under very diverse environmental conditions.     

Altered immune responsiveness in patients with chronic glomerulonephritis

In order to detect abnormalities in humoral immunity and to determine immunogenetic traits underlying chronic glomerulonephritis, sera from 260 patients who had chronic glomerulonephritis and who were undergoing hemodialysis were tested for naturally occurring antibodies against mycoplasma and 22 different viruses. Among the 23 microorganisms tested, antibody titers were significantly lower against 12, higher against 3, and no different against 8 when compared with titers of 43 normal subjects. The data were analyzed further by plotting each in a 23-dimensional space according to their standardized antibody titers. Multivariate cluster analysis by the Ward's method revealed 3 large clusters differing from each other in natural antibody titers, and one of the clusters included 74% of the normal controls, while two other distinct clusters comprised the majority of the patients. The level of BUN, creatinine, and duration of hemodialysis treatment did not differ significantly among patients in these three different clusters. Our study suggests that patients with chronic glomerulonephritis being treated by hemodialysis have altered levels of naturally occurring antibodies to microorganisms. This alteration is not caused by just the uremic state or hemodialysis but immunogenetic regulation may also play a part.