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1.
Animals (Basel) ; 14(3)2024 Jan 31.
Article in English | MEDLINE | ID: mdl-38338109

ABSTRACT

Napier grass (Pennisetum purpureum Schumach) supports a significant proportion of animal production in subtropical and tropical regions, but its quality is low and when offered alone, results in low ruminant production. Shifting the management of Napier grass towards a higher-quality feed increased milk yield and liveweight gain for small, mature cattle without supplementation. This review highlights the opportunity for further increases in milk and meat production for differing classes of livestock in the tropics and subtropics by improving the nutritive value of Napier grass using new best management practice flowing on to improve food security for the millions of people in these regions.

2.
Sci Rep ; 9(1): 8306, 2019 06 05.
Article in English | MEDLINE | ID: mdl-31165743

ABSTRACT

Endemic co-circulation of potentially zoonotic avian influenza viruses (AIV) of subtypes H5N1 and H9N2 (G1 lineage) in poultry in Bangladesh accelerated diversifying evolution. Two clinical samples from poultry obtained in 2016 yielded five different subtypes (highly pathogenic [HP] H5N1, HP H5N2, HP H7N1, HP H7N2, H9N2) and eight genotypes of AIV by plaque purification. H5 sequences grouped with clade 2.3.2.1a viruses while N1 was related to an older, preceding clade, 2.2.2. The internal genome segments of the plaque-purified viruses originated from clade 2.2.2 of H5N1 or from G1/H9N2 viruses. H9 and N2 segments clustered with contemporary H9N2 strains. In addition, HP H7 sequences were detected for the first time in samples and linked to Pakistani HP H7N3 viruses of 2003. The unexpected findings of mixtures of reassorted HP H5N1 and G1-like H9N2 viruses, which carry genome segments of older clades in association with the detection of HP H7 HA segments calls for confirmation of these results by targeted surveillance in the area of origin of the investigated samples. Hidden niches and obscured transmission pathways may exist that retain or re-introduce genome segments of older viruses or reassortants thereof which causes additional challenges for diagnosis, risk assessment and disease control.


Subject(s)
Influenza A Virus, H5N1 Subtype/genetics , Influenza A Virus, H7N3 Subtype/genetics , Influenza A Virus, H9N2 Subtype/genetics , Influenza in Birds/virology , Animals , Bangladesh/epidemiology , Chickens/virology , Evolution, Molecular , Genome, Viral , Genotype , Phylogeny , Reassortant Viruses , Risk Assessment , Virulence
3.
J Minim Access Surg ; 14(4): 357-361, 2018.
Article in English | MEDLINE | ID: mdl-29483376

ABSTRACT

Ureteral stricture resulting from chronic inflammations such as tuberculosis, recurrent stone disease and multiple endourological interventions are complex in nature; these may lead to severe adhesions to surrounding structures. Endourological management of these cases is difficult with poorer outcomes. In such situations, reconstructive surgical corrections remain a reliable option. We describe the technique of onlay and inlay buccal mucosal graft ureteroplasty using a robotic platform in management of complex ureteral strictures.

4.
Emerg Infect Dis ; 13(7): 1031-7, 2007 Jul.
Article in English | MEDLINE | ID: mdl-18214175

ABSTRACT

An encephalitis outbreak was investigated in Faridpur District, Bangladesh, in April-May 2004 to determine the cause of the outbreak and risk factors for disease. Biologic specimens were tested for Nipah virus. Surfaces were evaluated for Nipah virus contamination by using reverse transcription-PCR (RT-PCR). Thirty-six cases of Nipah virus illness were identified; 75% of case-patients died. Multiple peaks of illness occurred, and 33 case-patients had close contact with another Nipah virus patient before their illness. Results from a case-control study showed that contact with 1 patient carried the highest risk for infection (odds ratio 6.7, 95% confidence interval 2.9-16.8, p < 0.001). RT-PCR testing of environmental samples confirmed Nipah virus contamination of hospital surfaces. This investigation provides evidence for person-to-person transmission of Nipah virus. Capacity for person-to-person transmission increases the potential for wider spread of this highly lethal pathogen and highlights the need for infection control strategies for resource-poor settings.


Subject(s)
Communicable Diseases, Emerging/transmission , Cross Infection/transmission , Encephalitis, Viral/transmission , Henipavirus Infections/transmission , Nipah Virus/isolation & purification , Adolescent , Adult , Bangladesh/epidemiology , Case-Control Studies , Child , Child, Preschool , Communicable Diseases, Emerging/epidemiology , Communicable Diseases, Emerging/mortality , Confidence Intervals , Contact Tracing , Cross Infection/epidemiology , Cross Infection/mortality , Disease Outbreaks , Disease Transmission, Infectious , Encephalitis, Viral/epidemiology , Encephalitis, Viral/mortality , Environmental Microbiology , Female , Henipavirus Infections/epidemiology , Henipavirus Infections/mortality , Humans , Infant , Male , Middle Aged , Odds Ratio , Reverse Transcriptase Polymerase Chain Reaction , Risk Factors
5.
Tohoku J Exp Med ; 200(4): 211-29, 2003 Aug.
Article in English | MEDLINE | ID: mdl-14580152

ABSTRACT

Mismatched or damaged base pairs in DNA are mutagenic and both eukaryotes and prokaryotes have a series of repair systems that decrease a spontaneous mutation rate. All exocyclic amino groups of cytosine(C), adenine(A), and guanine(G) contribute to hydrogen bonds for base pairing. High temperature and oxidative stresses increase the deamination of these bases and methylated C. These deaminated sites would be initially recognized by components of DNA repair system. We discovered a novel G/thymine(T)-mismatch binding protein (nGTBP) that bound, with high affinity, to a minimal 14-mer DNA heteroduplex with a strict 5'-TRT GNB-3' sequence (R for purine, N for any bases, and B for "not A," namely for C, G, or T ). This italicized G position mismatched with T could be replaced by hypoxanthine, the deaminated A. The nGTBP, however, barely recognized DNA duplexes individually containing 8-oxo-G, thymine glycol, and 5-methylcytosine.


Subject(s)
Base Pair Mismatch , Base Sequence , DNA-Binding Proteins/metabolism , Guanine/metabolism , Thymidine/metabolism , Adenosine Triphosphatases/genetics , Adenosine Triphosphatases/metabolism , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Cell Line , DNA Damage , DNA Repair , DNA-Binding Proteins/genetics , Humans , Molecular Structure , MutS DNA Mismatch-Binding Protein , Nucleic Acid Conformation , Oxidation-Reduction , Tumor Suppressor Protein p53/genetics , Tumor Suppressor Protein p53/metabolism
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