scholarly journals A micro-epidemiological report on the unstable transmission of malaria in Aligarh, India

2020 ◽  
Vol 11 ◽  
pp. e00161
Author(s):  
Sana Aqeel ◽  
Ansari Naheda ◽  
Adil Raza ◽  
Wajihullah Khan
2012 ◽  
Vol 87 (5) ◽  
pp. 806-812 ◽  
Author(s):  
Melissa A. Rolfes ◽  
Matthew McCarra ◽  
Chandy C. John ◽  
Kacey C. Ernst ◽  
Kim A. Lindblade ◽  
...  

2004 ◽  
Vol 72 (9) ◽  
pp. 5135-5142 ◽  
Author(s):  
Chandy C. John ◽  
Ann M. Moormann ◽  
Peter O. Sumba ◽  
Ayub V. Ofulla ◽  
Daniel C. Pregibon ◽  
...  

ABSTRACT Gamma interferon (IFN-γ) responses to the Plasmodium falciparum antigens liver-stage antigen 1 (LSA-1) and thrombospondin-related adhesive protein (TRAP) are thought to be important in protection against malaria. Optimal methods of testing and the effects of age and transmission intensity on these responses are unknown. IFN-γ responses to LSA-1 and TRAP peptides were assessed by the enzyme-linked immunospot assay (ELISPOT) and enzyme-linked immunosorbent assay (ELISA) in children and adults from areas of stable and unstable malaria transmission in Kenya. Adults in the areas of stable and unstable transmission had similar frequencies and levels of IFN-γ responses to LSA-1 and TRAP as determined by ELISPOT and ELISA. In contrast, IFN-γ responses to the LSA-1 T3 peptide (assessed by ELISPOT) and to any LSA-1 peptide (assessed by ELISA) were less frequent in children in the area of unstable transmission than in children in the area of stable transmission. IFN-γ responses to LSA-1 were more frequently detected by ELISA than by ELISPOT in the stable-transmission area. IFN-γ responses detected by ELISA and ELISPOT did not correlate with each other. In children in the stable-transmission area, IFN-γ responses to LSA-1 peptides assessed by ELISA, but not by ELISPOT, were associated with protection against clinical malaria and anemia. IFN-γ responses to LSA-1 appear to require repeated P. falciparum exposure and/or increased age and, as measured by ELISA, are associated with protection against clinical malaria and anemia.


2016 ◽  
Vol 15 (1) ◽  
Author(s):  
Daniel M. Parker ◽  
Jordi Landier ◽  
Lorenz von Seidlein ◽  
Arjen Dondorp ◽  
Lisa White ◽  
...  

2009 ◽  
Vol 8 (1) ◽  
pp. 5 ◽  
Author(s):  
Asnakew K Yeshiwondim ◽  
Sucharita Gopal ◽  
Afework T Hailemariam ◽  
Dereje O Dengela ◽  
Hrishikesh P Patel

Genome ◽  
1991 ◽  
Vol 34 (1) ◽  
pp. 35-40 ◽  
Author(s):  
I. M. Ray ◽  
E. T. Bingham

Mutable alleles, typically regulated by transposable elements, have been identified in a number of plant species. Tissue culture induced genomic shocks may activate such elements. A mutable recessive condition arose in tissue culture of alfalfa and was highly unstable in subsequent cycles of culture. The mutable allele, designated c2-m4, is allelic to the C2 locus, a basic color factor locus involved in anthocyanin synthesis. Current research has focused on the inheritance and instability of c2-m4 in new genetic backgrounds as well as on dosage effects of the allele. We have confirmed a previous report that c2-m4 reverts to function at much higher frequencies in vitro (reversion frequency ca. 0.23) than in planta (reversion frequency < 0.001). Over sexual generations c2-m4 continues to be unstable. Transmission of the mutable phenotype to selfed, testcross, and F2 populations demonstrated monofactorial inheritance patterns (P > 0.25). In populations expected to have some plants carrying two or more c2-m4 alleles, individuals were found that reverted in vitro at significantly higher frequencies than their parent (0.67 ± 0.04 and 0.44 ± 0.08 versus 0.20 ± 0.09). In planta reversion also increased with increasing c2-m4 dosage. Preliminary evidence indicates that as c2-m4 dosage increases, each allele maintains its original capacity to revert.Key words: somaclonal variation, transposable element, tissue culture, mutable allele.


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