Nodavirus RNA replication crown architecture reveals proto-crown precursor and viral protein A conformational switching.

Positive-strand RNA viruses replicate their genomes in virus-induced membrane vesicles, and the resulting RNA replication complexes are a major target for virus control. Nodavirus studies first revealed viral RNA replication proteins forming a 12-fold symmetric "crown" at the vesicle opening to the cytosol, an arrangement recently confirmed to extend to distantly related alphaviruses. Using cryoelectron microscopy (cryo-EM), we show that mature nodavirus crowns comprise two stacked 12-mer rings of multidomain viral RNA replication protein A.

Tazobactam-induced haemolytic anaemia, possibly caused by non-immunological adsorption of IgG onto patient's red cells.

A patient with pneumonia was treated with Tazocin (piperacillin/tazobactam). However, the expected haemoglobin (Hb) increment after transfusion was not achieved. Plasma bilirubin and lactate dehydrogenase were raised.

A newly identified nonsecretor allele of the human histo-blood group alpha(1,2)fucosyltransferase gene (FUT2).

Background And Objectives: The human Secretor alpha(1, 2)fucosyltransferase gene determines the ABH secretor status and influences the Lewis phenotype of an individual. Studies were carried out on the Lewis (a+b-) nonsecretors of different groups indigenous to Taiwan to demonstrate their se genotypes.

Methods: The Lewis phenotype of the blood samples was determined by a microplate method.

Immunohematology in Taiwan.

There are major differences in the distribution of blood group antigens and antibodies between the different population groups of Taiwan and whites. As a result, standard Western pretransfusion testing procedures have been modified for use in Taiwan, resulting in great reductions in cost and labor. These differences, in addition to their influence on the clinical practise of transfusion medicine in Taiwan, are also important anthropologically, and it is hoped that more population groups in Asia can be investigated in the near future.

Heterogeneity of the human H blood group alpha(1,2)fucosyltransferase gene among para-Bombay individuals.

Background And Objectives: The para-Bombay phenotype has a relatively high frequency of about 1 in 8,000 Taiwanese. Studies were carried out on eight healthy and unrelated Taiwanese with the para-Bombay phenotype to cast light on its immunogenetic basis.

Materials And Methods: Blood and saliva samples were tested with standard hemagglutination techniques.

Comparison of the Lewis phenotypes among the different population groups of Taiwan.

In Caucasians, three red cell Lewis phenotypes are observed, namely Le (a+b-), Le (a-b+) and Le (a-b-). For Chinese living in Taiwan the Le (a+b-) phenotype is replaced by the Le (a+b+) phenotype so that the three red cell Lewis phenotypes observed in Chinese are Le (a+b+), Le (a-b+) and Le (a-b-). In addition, Chinese individuals with Le (a-b-) red cells can be subdivided into two groups, namely those who secrete both ABH and Lewis substances in saliva and those who secrete only ABH substances in saliva.

The development of ABO isohemagglutinins in Taiwanese.

To evaluate the developmental pattern of ABO isohemagglutinins in Taiwanese, 644 blood samples (349 males, 295 females), including cord blood, were collected from individuals with ages ranging from newborn to 83 years. Synthesis of anti-A and anti-B could be demonstrated in most Taiwanese infants by 2-4 months of age, increasing progressively to reach adult levels (titers of 1:32-1:256) at around 1 year of age. Peak levels were reached at between 3-10 years of age and then declined with advancing years, with individuals of 80 years of age and over showing reduced levels similar to those seen in 6- to 12-month-old infants.

The distribution of the MiIII (Gp.Mur) phenotype among the population of Taiwan.

The MiIII (Gp.Mur) phenotype is rare among Caucasians but has a much higher incidence among some Oriental populations. In Taiwan the population is relatively heterogenous and, as expected, the incidence of the MiIII phenotype was found to vary markedly among the different ethnic groups.

Heterogeneity of the human Secretor alpha(1,2)fucosyltransferase gene among Lewis(a+b-) non-secretors.

The human Secretor alpha (1,2)fucosyltransferase gene determines the ABH secretor status and influences the Lewis phenotype of an individual. Two different se alleles with point mutations, C571 to T and G849 to A respectively, in the coding region were identified in Le(a+b-) non-secretors from one of the Taiwanese indigenous groups. The base substitutions predict the alteration of Arg191 and Trp283 to stop codons respectively, resulting in deletion of the Secretor enzyme's C-terminal segment.

Correlation of a missense mutation in the human Secretor alpha 1,2-fucosyltransferase gene with the Lewis(a+b+) phenotype: a potential molecular basis for the weak Secretor allele (Sew).

A missense mutation (A385 to T), predicting an Ile129 to Phe substitution, in the human Secretor alpha 1,2-fucosyltransferase gene was present in double dose in Lewis(a+b+) individuals, but not in Lewis(a-b+) individuals. Co-segregation of the Lewis(a+b+) phenotype with homozygosity for the mutation was also verified. These results yield a potential molecular basis for the weak Secretor allele (Sew) accounting for the Lewis(a+b+) phenotype.

Identification of variant glycophorins of human red cells by lectinoblotting: application to the Mi.III variant that is relatively frequent in the Taiwanese population.

Background: Detection of normal and variant glycophorin electrophoretic bands with T- and Tn-specific lectins is based on the possibility of glycophorin transformation into T or Tn antigens by simple chemical modifications in the blot.

Study Design And Methods: Human red cell membrane proteins were fractionated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and blotted onto nitrocellulose. The blots were submitted to mild acid hydrolysis (desialylation of glycophorins exposing T antigens) and then to Smith degradation (degalactosylation of asialo-glycophorins exposing Tn antigens).

The Le(a) antigen and neonatal hyperbilirubinemia in Taiwan.

Neonatal jaundice is known to be more severe in Taiwanese infants than in Caucasian infants. Although ABO fetomaternal incompatibility and glucose-6-phosphate dehydrogenase deficiency have been shown to play a role in the etiology of neonatal jaundice in some Taiwanese infants, the etiology in the majority of cases is unknown. In this study we found that in Taiwanese newborn infants, the red cell Le(a) antigen appeared later in infants who were jaundiced (peak serum bilirubin levels of > 12 mg/dl during the first week of life) than in infants who were not.

The incidence and significance of anti-"Mia" in Taiwan.

Background: The incidence of the Mill phenotype among Chinese blood donors in Taiwan is 7.3 percent. Anti-"Mia" is the most frequently occurring alloantibody of potential clinical significance encountered among Chinese patients in Taiwan, with a frequency of 0.

Modification of standard Western pretransfusion testing procedures for Taiwan.

Due to significant differences in blood group antigen and antibody frequencies between Taiwanese and Caucasians, standard Western pretransfusion testing procedures have been modified for use in Taiwan. Pretransfusion testing consists simply of ABO grouping and antibody screening/major cross-matching using the manual Polybrene method without any antiglobulin phase. The manual Polybrene method is preformed using regents prepared in house and is rapid (about 3 min), inexpensive and easy to perform.

Hemolytic disease of the newborn caused by maternal anti-Dib: a case report in Taiwan.

Possibly the first case of hemolytic disease caused by anti-Dib in a Chinese infant is reported. The infant developed jaundice soon after birth; based on study, the jaundice has been diagnosed as a result of maternal anti-Dib which was most likely induced by previous pregnancies. The phenotype of the mother's red cells was Di (a+b-).

The Lewis blood group system among Chinese in Taiwan.

The nonsecretor gene se is absent (or very rare) among Chinese in Taiwan and the previously reported Le(a+b-) phenotype in this population is in fact Le(a+b+) as proven by the presence of small amounts of Leb antigen on red blood cells. Salivary ABH substances in this phenotype are usually (although not always) markedly reduced. The Chinese Le(a+b+) phenotype is postulated to be the result of a weak secretor gene Se omega.

Blood transfusion in the para-Bombay phenotype.

The H-deficient phenotypes found in Chinese so far, have all been secretors of soluble blood group substances in saliva. The corresponding isoagglutinin activity (e.g.

The distribution of blood group antigens and alloantibodies among Chinese in Taiwan.

Most blood group antigens among Chinese people are very homogeneous (e.g., D, 99.