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56 results for “Camellia sinensis”
Fig. 7. a in Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
Fig. 7. a) A section of the small intestine in GV revealed normal villous architecture with a normal brush border (H&E stain, X200); b) Sections examined from the liver in this group showed preserved hepatic lobular architecture (H&E stain, X200).
Fig. 6. a in Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
Fig. 6. a) A section of the small intestine in GIV revealed marked villous broadening (red line) with decreased villous height to crypt length ratio. There was dense infiltration by mononuclear inflammatory cells within the villous core (green arrows), degeneration of the villous tip-regions (black arrows), and increased mucin production (H&E stain, X200). b) Sections from the small intestine revealed many adherents (red arrows) and separate (black arrows) Cryptosporium stages, probably oocyst (H&E stain, X1000). c)Sections examined from the liver in this group showed hepatocellular degeneration (black arrow) and focal mononuclear cellular infiltration (red arrows) (H&E stain, X200)
Fig. 5. a in Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
Fig. 5. a) A section of the small intestine in GIII revealed moderate villous broadening, infiltration by mononuclear inflammatory cells within the villous core (red arrow), focal degeneration of the villous tip regions (black arrow), and increased mucin production (H&E stain, X200). b) Sections examined from the liver in this group showed focal mononuclear cellular infiltration (red arrow) (H&E stain, X200).
Fig. 3. a in Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
Fig. 3. a) A section of the small intestine in GI revealed villous broadening (red line) with an expansion of the villous core by mononuclear inflammatory cells (black arrow) (H&E stain, X200); b) Sections examined from the liver in this group showed preserved hepatic lobular architecture and cloudy swelling of hepatocytes (H&E stain, X200).
Fig. 1. a in Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
Fig. 1. a) Cryptosporidium oocyst (stained red to deep purple with the modified Ziehl–Neelsen method); b) immunofluorescence staining of Cryptosporidium oocyst (ovoid or spherical brilliant apple/ green structure)
Fig. 2 in Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
Fig. 2. Agarose gel electrophoresis showing: Lane 1: 50 bp DNA molecular weight marker, Lane 2: Positive control, Lane 3: Negative control, Lane 4: Positive sample of nested PCR products targeting COWP gene of Cryptosporidium at 553 bp, Lane 5: 50 bp DNA molecular weight marker, and Lane 6: RFLP products of the sample after digestion with RsaI endonuclease (C. parvum genotype 2 digestion products at 410, 106, and 34 (too small to be detected) bp.
Fig. 4. a in Anti-cryptosporidial activity of Camellia sinensis (green tea extract) in experimentally infected immunocompromised mice
Fig. 4. a) A section of the small intestine in GII revealed returning of the normal villous pattern, normal mucosa, and goblet cells (H&E stain, X200). b) Sections examined from the liver in this group showed preserved hepatic lobular architecture (H&E stain, X200).
Camellia sinensis decontaminated gx
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FIGURES 3–6 in A new whitefly genus and species, Aleuroparvus theae Dubey (Hemiptera: Aleyrodidae) colonising Assam tea (Camellia sinensis) and Cinnamomum bejolghota, in North-East India
FIGURES 3–6. Aleuroparvus theae gen. et sp. nov., camera lucida drawings, 3, puparium, dorsal and ventral views; 4, thoracic tracheal pore and submarginal wax gland; 5, vasiform orifice and caudal furrow; 6, legs and antenna.
FIGURES 21–27 in A new whitefly genus and species, Aleuroparvus theae Dubey (Hemiptera: Aleyrodidae) colonising Assam tea (Camellia sinensis) and Cinnamomum bejolghota, in North-East India
FIGURES 21–27 Aleuroparvus theae gen. et sp. nov., scanning electron microscope images, puparium, 21, dorsal view; 22, abdominal area; 23, caudal furrow; 24, margin and submarginal bands; 25, thoracic tracheal pore opening; 26, submarginal wax gland; 27, eighth abdominal setae (broken), vasiform orifice and caudal furrow.
FIGURES 28–33 in A new whitefly genus and species, Aleuroparvus theae Dubey (Hemiptera: Aleyrodidae) colonising Assam tea (Camellia sinensis) and Cinnamomum bejolghota, in North-East India
FIGURES 28–33. Aleuroparvus theae gen. et sp. nov., scanning electron microscope images, puparium, 28, puparium, ventrolateral view showing obliquely downward extension of submargin; 29, ventral view; 30, thoracic tracheal fold; 31, legs, rostrum and adhesive sacs; 32, ventral setae and caudal tracheal fold; 33, antenna (RS– rostrum, AP– adhesive pads, ANT– antenna).
FIGURES 1–2 in A new whitefly genus and species, Aleuroparvus theae Dubey (Hemiptera: Aleyrodidae) colonising Assam tea (Camellia sinensis) and Cinnamomum bejolghota, in North-East India
FIGURES 1–2. Aleuroparvus theae gen. et sp. nov., habitus, 1, puparium on Cinnamomum bejolghota showing white wax secretion at thoracic tracheal pore area, and submarginal ridge; 2, puparium on tea leaf.
FIGURES 7–14 in A new whitefly genus and species, Aleuroparvus theae Dubey (Hemiptera: Aleyrodidae) colonising Assam tea (Camellia sinensis) and Cinnamomum bejolghota, in North-East India
FIGURES 7–14. Aleuroparvus theae gen. et sp. nov., photomicrographs, holotype puparium, 7, dorsal and ventral views; 8, margin, tracheal pore, submarginal wax secreting gland; 9, cephalothorax, partly separated submargin; 10, abdominal segment sutures, pockets and depressions; 11, submarginal wax glands and geminate pores; 12, vasiform orifice, caudal furrow and 8th abdominal setae; 13, cephalic seta; 14, first abdominal seta (FAS– first abdominal seta).
FIGURES 15–20 in A new whitefly genus and species, Aleuroparvus theae Dubey (Hemiptera: Aleyrodidae) colonising Assam tea (Camellia sinensis) and Cinnamomum bejolghota, in North-East India
FIGURES 15–20. Aleuroparvus theae gen. et sp. nov., photomicrographs, paratype puparium, dorsal and ventral views, 15, submarginal wax secreting gland laterad of abdominal segment V; 16, ventral surface, separated; 17, cephalothorax, adhesive pads; 18, thoracic tracheal fold; 19, imprints of abdominal segment sutures and stomata; 20, ventral 8th abdominal setae, caudal fold.
FIGURE 4 in New records of Pestalotioid species associated with leaf spot disease on Camellia sinensis from northern Thailand
FIGURE 4. Pseudopestalotiopsis chinensis (MFLU23-0398 (a–e), MFLUCC 23-0261 (f–r), new geographical record). a Diseased leaf of Camellia sinensis var. assamica. b Close-up of the lesion. c Acervular fruiting bodies on the lesion. d Section of a fruiting body on specimen. e Conidiogenous cells of a fruiting body on the specimen. f Upper view of culture on the PDA (at 25 °C). g Reverse view of culture on the PDA (at 25 °C). h–i Pycnidia on the PDA. j Mycelium on the PDA. k–l Conidiogenous cells in culture. m–r Conidia. Scale bars: d, k–r = 20 μm, e = 5 μm, i =100 μm, j = 200 μm.
FIGURE 1 in New records of Pestalotioid species associated with leaf spot disease on Camellia sinensis from northern Thailand
FIGURE 1. Maximum-likelihood tree inferred by IQ-TREE analysis of the combined ITS, tub2 and tef1-α sequence data. Bootstrap support values for maximum likelihood (ML) / maximum parsimony (MP) ≥ 50% and Bayesian posterior probability values (BYPP) ≥ 0.80 are given at the nodes (MLBS/ MPBS/ BYPP). The tree is rooted with Pestalotiopsis diversiseta (MFLUCC 12-0287) and P. spathulata (CBS 356.86). Type species are indicated in bold, and the newly generated strains are in bold red.
Camellia sinensis SPAdes preassembly
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Camellia sinensis SPAdes preassembly
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Fig. 3 in Transcriptome and metabolome profiling unveiled mechanisms of tea (Camellia sinensis) quality improvement by moderate drought on pre-harvest shoots
Fig. 3. Transcriptome analysis of DEGs. (A) Venn diagram of DEGs. (B–D) Biological processes of corresponding DEGs related to differentially accumulated metabolites in groups of CK vs. MI, CK vs. MO, and CK vs. SE.
Fig. 1 in Transcriptome and metabolome profiling unveiled mechanisms of tea (Camellia sinensis) quality improvement by moderate drought on pre-harvest shoots
Fig. 1. Metabolomic analysis of differentially accumulated metabolites. (A) Venn diagram of differentially accumulated metabolites. (B) The top five most abundant categories. A, amino acids and derivatives; F, flavonoids; N, nucleotide and derivatives; L, lipids; O, organic acids. Blue dot, categories with less metabolites. (C) Accumulation tendencies of the five categories under diferent SWCs.. CK, control (21–24% SWC); MI, milder drought (15–18% SWC); MO, moderate drought (12–15% SWC); SE, severe drought (9–12% SWC). (D) KEGG enrichment of group CK vs. MI from metabolic data. (E) KEGG enrichment of group CK vs. MO from metabolic data. (F) KEGG enrichment of group CK vs. SE from metabolic data. Plot: mean with standard deviation (SD). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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