scholarly journals COVID-19-associated-mucormycosis: possible role of free iron uptake and immunosuppression

Author(s):  
Tahani Tabassum ◽  
Yusha Araf ◽  
Abu Tayab Moin ◽  
Tanjim Ishraq Rahaman ◽  
Mohammad Jakir Hosen
Keyword(s):  
Author(s):  
Chandrika N. Deshpande ◽  
Aaron P. McGrath ◽  
Josep Font ◽  
Amy P. Guilfoyle ◽  
Megan J. Maher ◽  
...  

FeoB is a transmembrane protein involved in ferrous iron uptake in prokaryotic organisms. FeoB comprises a cytoplasmic soluble domain termed NFeoB and a C-terminal polytopic transmembrane domain. Recent structures of NFeoB have revealed two structural subdomains: a canonical GTPase domain and a five-helix helical domain. The GTPase domain hydrolyses GTP to GDP through a well characterized mechanism, a process which is required for Fe2+transport. In contrast, the precise role of the helical domain has not yet been fully determined. Here, the structure of the cytoplasmic domain of FeoB fromGallionella capsiferriformansis reported. Unlike recent structures of NFeoB, theG. capsiferriformansNFeoB structure is highly unusual in that it does not contain a helical domain. The crystal structures of both apo and GDP-bound protein forms a domain-swapped dimer.


2004 ◽  
Vol 186 (5) ◽  
pp. 1409-1414 ◽  
Author(s):  
Heather P. Benson ◽  
Kristin LeVier ◽  
Mary Lou Guerinot

ABSTRACT In many bacteria, the ferric uptake regulator (Fur) protein plays a central role in the regulation of iron uptake genes. Because iron figures prominently in the agriculturally important symbiosis between soybean and its nitrogen-fixing endosymbiont Bradyrhizobium japonicum, we wanted to assess the role of Fur in the interaction. We identified a fur mutant by selecting for manganese resistance. Manganese interacts with the Fur protein and represses iron uptake genes. In the presence of high levels of manganese, bacteria with a wild-type copy of the fur gene repress iron uptake systems and starve for iron, whereas fur mutants fail to repress iron uptake systems and survive. The B. japonicum fur mutant, as expected, fails to repress iron-regulated outer membrane proteins in the presence of iron. Unexpectedly, a wild-type copy of the fur gene cannot complement the fur mutant. Expression of the fur mutant allele in wild-type cells leads to a fur phenotype. Unlike a B. japonicum fur-null mutant, the strain carrying the dominant-negative fur mutation is unable to form functional, nitrogen-fixing nodules on soybean, mung bean, or cowpea, suggesting a role for a Fur-regulated protein or proteins in the symbiosis.


1990 ◽  
Vol 271 (1) ◽  
pp. 1-9 ◽  
Author(s):  
K Thorstensen ◽  
I Romslo

Hepatology ◽  
2008 ◽  
Vol 47 (5) ◽  
pp. 1737-1744 ◽  
Author(s):  
Anita C.G. Chua ◽  
Carly E. Herbison ◽  
Sarah F. Drake ◽  
Ross M. Graham ◽  
John K. Olynyk ◽  
...  
Keyword(s):  

2011 ◽  
Vol 13 (11) ◽  
pp. 2990-2999 ◽  
Author(s):  
Chana Kranzler ◽  
Hagar Lis ◽  
Yeala Shaked ◽  
Nir Keren
Keyword(s):  

Parasitology ◽  
2010 ◽  
Vol 137 (6) ◽  
pp. 899-917 ◽  
Author(s):  
M. C. TAYLOR ◽  
J. M. KELLY

SUMMARYIron is almost ubiquitous in living organisms due to the utility of its redox chemistry. It is also dangerous as it can catalyse the formation of reactive free radicals – a classical double-edged sword. In this review, we examine the uptake and usage of iron by trypanosomatids and discuss how modulation of host iron metabolism plays an important role in the protective response. Trypanosomatids require iron for crucial processes including DNA replication, antioxidant defence, mitochondrial respiration, synthesis of the modified base J and, in African trypanosomes, the alternative oxidase. The source of iron varies between species. Bloodstream-form African trypanosomes acquire iron from their host by uptake of transferrin, andLeishmania amazonensisexpresses a ZIP family cation transporter in the plasma membrane. In other trypanosomatids, iron uptake has been poorly characterized. Iron-withholding responses by the host can be a major determinant of disease outcome. Their role in trypanosomatid infections is becoming apparent. For example, the cytosolic sequestration properties of NRAMP1, confer resistance against leishmaniasis. Conversely, cytoplasmic sequestration of iron may be favourable rather than detrimental toTrypanosoma cruzi. The central role of iron in both parasite metabolism and the host response is attracting interest as a possible point of therapeutic intervention.


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