ABSTRACT
The article highlighted the problem of meat cattle genetic defects. The aim was the development of DNA tests for some genetic defects diagnostics, the determination of the animal carriers and their frequencies tracking in time. The 1490 DNA samples from the Aberdeen Angus (n = 701), Hereford (n = 385), Simmental (n = 286) and Belgian Blue (n = 118) cattle have been genotyped on the genetic defects by newly created and earlier developed DNA tests based on AS-PCR and PCR-RFLP methods. The Aberdeen Angus cattle genotyping has revealed 2.38 ± 0.31% AMC-cows and 1.67 ± 0.19 % AMC-bulls, 0.65 ± 0.07% DDC-cows and 0.90 ± 0.10% DDC-bulls. The single animals among the Hereford cattle were carriers of MSUD and CWH (on 0.27 ± 0.05%), ICM and HY (on 0.16 ± 0.03%). The Simmental cattle were free from OS. All Belgian Blue livestock were M1- and 0.84%-CMD1-carriers. The different ages Aberdeen Angus cattle genotyping has shown the tendency of the AMC- and DDC frequencies to increase in the later generations. The statistically significant increase of DDC of 1.17% in the cows' population born in 2019 compared to those born in 2015 allows concluding the further development of the DNA analysis-based measures preventing the manifestation of the genetic anomalies in meat cattle herds is necessary.
Subject(s)
Cattle Diseases/genetics , Cattle/genetics , Genetic Carrier Screening/veterinary , Animals , Cattle Diseases/diagnosis , Genetic Carrier Screening/methods , Genetic Carrier Screening/standards , Genotyping Techniques/methods , Genotyping Techniques/standards , Genotyping Techniques/veterinary , Polymerase Chain Reaction/methods , Polymerase Chain Reaction/standards , Sensitivity and SpecificityABSTRACT
Giardia duodenalis is divided into eight assemblages (named A to H). Isolates of assemblage A are divided into four sub-assemblages (AI, AII, AIII and AIV). While isolates of sub-assemblage AII are almost exclusively detected in human hosts, isolates of assemblage B are encountered in a multitude of animal hosts and humans. Here, we isolated single cysts of G. duodenalis from a human stool sample and found that one of them had overlaps of assemblage AII and B alleles and an unexpectedly high number of variants of the beta-giardin (Bg) and GLORF-C4 (OrfC4) alleles. In addition, one of the Bg alleles of that cyst had a fragment of sub-assemblage AII interspersed with fragments of assemblage B, thus indicating that this allele may be a recombinant between sequences A and B. Our results are unprecedented and put a check on the statement that different assemblages of G. duodenalis represent species with different host specificities.
Subject(s)
Alleles , Cysts/genetics , Cytoskeletal Proteins/genetics , Genetic Carrier Screening , Giardia lamblia/genetics , Protozoan Proteins/genetics , Animals , Genetic Carrier Screening/veterinary , Genotype , Giardia lamblia/classificationABSTRACT
Abstract Giardia duodenalis is divided into eight assemblages (named A to H). Isolates of assemblage A are divided into four sub-assemblages (AI, AII, AIII and AIV). While isolates of sub-assemblage AII are almost exclusively detected in human hosts, isolates of assemblage B are encountered in a multitude of animal hosts and humans. Here, we isolated single cysts of G. duodenalis from a human stool sample and found that one of them had overlaps of assemblage AII and B alleles and an unexpectedly high number of variants of the beta-giardin (Bg) and GLORF-C4 (OrfC4) alleles. In addition, one of the Bg alleles of that cyst had a fragment of sub-assemblage AII interspersed with fragments of assemblage B, thus indicating that this allele may be a recombinant between sequences A and B. Our results are unprecedented and put a check on the statement that different assemblages of G. duodenalis represent species with different host specificities.
Resumo A espécie Giardia duodenalis é dividida em oito grupos (nomeados de A a H). Isolados do grupo A são divididos em quatro subgrupos (AI, AII, AIII and AIV). Enquanto isolados do subgrupo AII são detectados quase exclusivamente em hospedeiros humanos, isolados do subgrupo B são encontrados em uma grande variedade de hospedeiros entre animais e humanos. Neste trabalho, foi constatado que, dentre diversos cistos individualizados de G. duodenalis provenientes de fezes de origem humana, um cisto continha os alelos AII e B e um número inesperado de variantes de alelos codificadores de beta giardina e GLORF-C4. Ainda, um dos alelos beta giardina desse cisto possuía fragmentos AII intercalando um fragmento B, indicando que esse alelo pode ser um recombinante entre alelos AII e B. Os resultados aqui apresentados são inéditos e colocam em dúvida o conceito atual de que os diferentes grupos de G. duodenalis representam espécies distintas com diferentes graus de especificidade por hospedeiros.
Subject(s)
Animals , Protozoan Proteins/genetics , Giardia lamblia/genetics , Cysts/genetics , Cytoskeletal Proteins/genetics , Alleles , Genetic Carrier Screening/veterinary , Giardia lamblia/classification , GenotypeABSTRACT
The identification of phenotypically normal carriers of genetic defects is crucial for eliminating recessive defect genes from farm animal populations. Recombinant DNA techniques allow us to identify defect genes on the DNA-basis regardless of the animals age and time of gene expression. Genetic defects also are important as model systems to investigate the regulation of metabolic pathways and the mechanisms of embryonic development.
Subject(s)
Animals, Domestic/genetics , Cloning, Molecular , Genetic Carrier Screening/veterinary , Genetic Diseases, Inborn/veterinary , Animals , DNA/genetics , Genetic Diseases, Inborn/genetics , Polymorphism, Restriction Fragment LengthABSTRACT
The paper presents the results of some genetic studies accomplished in Romania in the field of pathology of reproduction in domestic animals (pseudohermaphroditism in horses, testicular hypoplasia in he-goats, intersexuality in pigs, freemartinism and genital infantilism in cattle). Also, the use of the cytogenetic test in genetic prophylaxis in pigs and cattle was shown. In addition, the methods for detecting genitors with undesirable genes were devised and perspectives for the development of hereditary hygiene discussed.
