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Kakar, N.

Publications and source records attributed to Kakar, N..

2 recordsLinked to original sources

Field and lab phenomics facilitate detection of genetic variation for iron deficiency chlorosis tolerance in sorghum

Bioavailability of iron, an essential micronutrient to plants, is low in alkaline or calcareous soils, which are prevalent across semi-arid production regions. Breeding efforts to increase tolerance to iron deficiency chlorosis (IDC) in sorghum, a major crop of semi-arid regions, are confounded by spatial variation of stress severity in field trials. Here we developed and validated two high-throughput phenotyping approaches to address this challenge, with multi-spectral aerial imaging in the field and a controlled-environment assay to isolate the effects of iron bioavailability. In the field, severity and uniformity of stress are highly predictive of genetic signals for IDC tolerance (R2 > 0.6 for soil pH metrics and H2). Plot-level data filtering for stress conditions based on control genotypes successfully addresses field spatial variation (unfiltered H2 = 0.18 vs. filtered H2 = 0.4). The controlled-environment assay proxies field stress using iron sources with differential bioavailability, evidenced by high heritability ( H2 = 0.98) and phenotypic differential for hybrid control genotypes that matches field performance. Finally, we show that assay phenotypes are suitable for genome-wide association studies in global germplasm. Together, these field and lab phenomic approaches can be deployed to understand genetics of IDC tolerance and develop crops resilient to alkaline soils. HIGHLIGHTStress severity and uniformity greatly impact detection of genetic signals underlying iron deficiency chlorosis tolerance in sorghum. A controlled-environment assay reduces spatial heterogeneity and improves assessment of tolerance genetics.

genetics↗

Pneumococcal metabolic adaptation and colonization is regulated by the two-component regulatory system 08

Streptococcus pneumoniae two-component regulatory systems (TCS) enable adaptation and ensure its maintenance in host environments. This study deciphers the impact of the TCS08 on pneumococcal gene expression and its role in metabolic and pathophysiological processes. Transcriptome analysis and real-time PCR demonstrated a regulatory effect of the TCS08 on genes involved mainly in environmental information processing, intermediary metabolism, and colonization by S. pneumoniae D39 and TIGR4. Striking examples are genes of the fatty acid biosynthesis, arginine-deiminase system, and psa operon encoding the manganese ABC transport system. In silico analysis confirmed that TCS08 is homologous to Staphylococcus aureus SaeRS and a SaeR-like binding motif is displayed in the promotor region of pavB, the upstream gene of the tcs08 operon encoding a surface-exposed adhesin. Indeed, PavB is regulated by the TCS08 as confirmed by immunoblotting and surface abundance assays. Similarly, Pilus-1 of TIGR4 is regulated by TCS08. Finally, in vivo infections using the acute pneumonia and sepsis models showed a strain dependent effect. Loss of function of HK08 or TCS08 attenuated D39 virulence in lung infections. The RR08 deficiency attenuated TIGR4 in pneumonia, while there was no effect on sepsis. In contrast, lack of HK08 procured a highly virulent TIGR4 phenotype in both pneumonia and sepsis infections. Taken together, these data indicate the importance of TCS08 in pneumococcal fitness to adapt to the milieu of the respiratory tract during colonization.\n\nIMPORTANCEStreptococcus pneumoniae interplays with its environment by using 13 two-component regulatory systems and one orphan response regulator. These systems are involved in the sensing of environmental signals thereby modulating pneumococcal pathophysiology. This study aimed to understand the functional role of genes subject to control by the TCS08. The identified genes play a role in transport of compounds such as sugars or amino acids. In addition, the intermediary metabolism and colonization factors are modulated by TCS08. Thus, TCS08 regulates genes involved in maintaining pneumococcal physiology, transport capacity and adhesive factors to enable optimal colonization, which represents a prerequisite for invasive pneumococcal disease.

microbiology↗