Neither Hippurate-negative <Emphasis Type="Italic">Brachyspira pilosicoli</Emphasis> nor <Emphasis Type="Italic">Brachyspira pilosicoli</Emphasis> Type Strain Caused Diarrhoea in Early-weaned Pigs by Experimental Infection

A hippurate-negative biovariant of Brachyspira pilosicoli (B. pilosicoli ^hipp-) is occasionally isolated in diarrhoeic pigs in Finland, often concomitantly with hippurate-positive B. pilosicoli or Lawsonia intracellularis. We studied pathogenicity of B. pilosicoli ^hipp- with special attention paid to avoiding co-infection with other enteric pathogens. Pigs were weaned and moved to barrier facilities at the age of 11 days. At 46 days, 8 pigs were inoculated with B. pilosicoli ^hipp- strain Br1622, 8 pigs were inoculated with B. pilosicoli type strain P43/6/78 and 7 pigs were sham-inoculated. No signs of spirochaetal diarrhoea were detected; only one pig, inoculated with P43/6/78, had soft faeces from day 9 to 10 post inoculation. The pigs were necropsied between days 7 and 23 after inoculation. Live pigs were culture-negative for Brachyspira spp., but B. pilosicoli ^hipp- was reisolated from necropsy samples of two pigs. The lesions on large colons were minor and did not significantly differ between the three trial groups. In silver-stained sections, invasive spirochaetes were detected in colonic mucosae of several pigs in all groups. Fluorescent in situ hybridisation for genus Brachyspira, B. pilosicoli and strain Br1622 was negative. However, in situ detection for members of the genus Leptospira was positive for spirochaete-like bacteria in the colonic epithelium of several pigs in both infected groups as well as in the control group. L. intracellularis, Salmonella spp., Yersinia spp. and intestinal parasites were not detected. The failure of B. pilosicoli strains to cause diarrhoea is discussed with respect to infectivity of the challenge strains, absence of certain intestinal pathogens and feed and management factors.     

Models of the bis-histidine-coordinated ferricytochromes: Mössbauer and EPR spectroscopic studies of low-spin iron(III) tetrapyrroles of various electronic ground states and axial ligand orientations

The EPR and magnetic Mössbauer spectra of a series of axial ligand complexes of tetrakis(2,6-dimethoxyphenyl)porphyrinatoiron(III), [(2,6-(OMe)₂)₄TPPFeL₂]⁺, where L=N-methylimidazole, 2-methylimidazole, or 4-(dimethylamino)pyridine, of one axial ligand complex of tetraphenylporphyrin, the bis(4-cyanopyridine) complex [TPPFe(4-CNPy)₂]⁺, and of one axial ligand complex of tetraphenylchlorin, [TPCFe(ImH)₂]⁺, where ImH=imidazole, have been investigated and compared to those of low-spin Fe(III) porphyrinates and ferriheme proteins reported in the literature. On the basis of this and previous complementary spectroscopic investigations, three types of complexes have been identified: those having (d_xy)²(d_xz,d_yz)³ electronic ground states with axial ligands aligned in perpendicular planes (Type I), those having (d_xy)²(d_xz,d_yz)³ electronic ground states with axial ligands aligned in parallel planes (Type II), and those having the novel (d_xz,d_yz)⁴(d_xy)¹ electronic ground state (Type III). A subset of the latter type, with planar axial ligands aligned parallel to each other or strong macrocycle asymmetry that yield rhombic EPR spectra, cannot be created using the porphyrinate ligand. Type I centers are characterized by "large g_max" EPR spectra with g>3.2 and well-resolved, widely spread magnetic Mössbauer spectra having A_zz/g_NN>680 kG, with A_xx negative in sign but much smaller in magnitude than A_zz, while Type II centers have well-resolved rhombic EPR spectra with g_zz=2.4–3.1 and also less-resolved magnetic Mössbauer spectra, and usually have A_zz/g_NN in the range of 440–660 kG (but in certain cases as small as 180 kG) and A_xx again negative in sign but only somewhat smaller (but occasionally larger in magnitude) than A_zz, and Type III centers have axial EPR spectra with g_┴2.6 or smaller and g_║<1.0–1.95, but often not resolved, and less-resolved magnetic Mössbauer spectra having A_zz/g_NN in the range of 270–400 kG, and A_xx again negative in sign but much smaller in magnitude than A_zz. An exception to this rule is [TPPFe(4-CNPy)₂]⁺, which has A_xx/g_NN=–565 kG, A_yy/g_NN=629 kG, and A_zz/g_NN=4 kG. A subset of Type II complexes (Type II) have rhombicities (V/) much greater than 0.67 and A_zz/g_NN ranging from 320 to 170 kG, with A_xx also negative but with the magnitude of A_xx significantly larger than that of A_zz. These classifications are also observed for a variety of ferriheme proteins, and they lead to linear correlations between A_zz and either A_xx, g_zz, or V/ for Types I and II (but not for A_zz versus V/ for Type II). Not enough data are yet available on Type III complexes to determine what, if any, correlations may be observed.Abbreviations CCP cytochrome c peroxidase - 4-CNPy 4-cyanopyridine - cyt cytochrome - EFG electric field gradient - ESEEM electron spin echo envelope modulation - ImH imidazole - Mb myoglobin - MCD magnetic circular dichroism - 2-MeImH 2-methylimidazole - N-MeIm N-methylimidazole - 3NH₂PzH 3-aminopyrazole - 4-NMe₂Py 4-(dimethylamino)pyridine - [2,6-(OMe)₂]₄TPP dianion of tetrakis(meso-2,6-dimethoxyphenyl)porphyrin - OEiBC dianion of octaethylisobacteriochlorin - OEP dianion of octaethylporphyrin - PPIX dianion of protoporphyrin IX - Py pyridine - TMP dianion of meso-tetramesitylporphyrin - TPC dianion of meso-tetraphenylchlorin - TPP dianion of meso-tetraphenylporphyrin - 2,6-XylylNC 2,6-xylyl isocyanide     

Granulocyte-CSF induced inflammation-associated cardiac thrombosis in iron loading mouse heart and can be attenuated by statin therapy

Background  

Granulocyte colony-stimulating factor (G-CSF), a hematopoietic cytokine, was recently used to treat patients of acute myocardial infarction with beneficial effect. However, controversy exists as some patients developed re-stenosis and worsened condition post G-CSF delivery. This study presents a new disease model to study G-CSF induced cardiac thrombosis and delineate its possible mechanism. We used iron loading to mimic condition of chronic cardiac dysfunction and apply G-CSF to mice to test our hypothesis.     

Can short-term fasting protect against doxorubicin-induced cardiotoxicity?

Doxorubicin(Dox) is one of the most effective chemotherapeutic agents used in the treatment of several types of cancer. However the use is limited by cardiotoxicity. Despite extensive investigation into the mechanisms of toxicity and preventative strategies, Dox-induced cardiotoxicity still remains a major cause of morbidity and mortality in cancer survivors. Thus, continued research into preventative strategies is vital. Short-term fasting has proven to be cardioprotective against a variety of insults. Despite the potential, only a few studies have been conducted investigating its ability to prevent Dox-induced cardiotoxicity. However, all show proof-of-principle that short-term fasting is cardioprotective against Dox. Fasting affects a plethora of cellular processes making it difficult to discern the mechanism(s) translating fasting to cardioprotection, but may involve suppression of insulin and insulin-like growth factor-1 signaling with stimulated autophagy. It is likely that additional mechanisms also contribute. Importantly, the literature suggests that fasting may enhance the antitumor activity of Dox. Thus, fasting is a regimen that warrants further investigation as a potential strategy to prevent Dox-induced cardiotoxicity. Future research should aim to determine the optimal regimen of fasting, confirmation that this regimen does not interfere with the antitumor properties of Dox, as well as the underlying mechanisms exerting the cardioprotective effects.     

Conserved and divergent patterns of expression of DAZL,VASA and OCT4 in the germ cells of the human fetal ovary and testis

Background  

Germ cells arise from a small group of cells that express markers of pluripotency including OCT4. In humans formation of gonadal compartments (cords in testis, nests in ovary) takes place during the 1st trimester (6–8 weeks gestation). In the 2nd trimester germ cells can enter meiotic prophase in females whereas in males this does not occur until puberty. We have used qRTPCR, Westerns and immunohistochemical profiling to determine which of the germ cell subtypes in the human fetal gonads express OCT4, DAZL and VASA, as these have been shown to play an essential role in germ cell maturation in mice.     

1H and 13C NMR spectroscopic studies of the ferriheme resonances of three low-spin complexes of wild-type nitrophorin 2 and nitrophorin 2(V24E) as a function of pH

The ferriheme resonances of the low-spin (S = 1/2) complexes of wild-type (wt) nitrophorin 2 (NP2) and its heme pocket mutant NP2(V24E) with imidazole (ImH), histamine (Hm), and cyanide (CN⁻) as the sixth ligand have been investigated by NMR spectroscopy as a function of pH (4.0–7.5). For the three wt NP2 complexes, the ratio of the two possible heme orientational isomers, A and B, remains almost unchanged (ratio of A:B approximately 1:6 to 1:5) over this wide pH range. However, strong chemical exchange cross peaks appear in the nuclear Overhauser effect spectroscopy/exchange spectroscopy (NOESY/EXSY) spectra for the heme methyl resonances at low pH (pH* 4.0–5.5), which indicate chemical exchange between two species. We have shown these to be two different exogenous ImH or Hm orientations that are denoted B and B′, with the ImH plane nearly parallel and perpendicular to the ImH plane of the protein-provided His57, respectively. The wt NP2–CN complex also shows EXSY cross peaks due to chemical exchange, which is shown to be a result of interchange between two ruffling distortions of the heme. The same ruffling distortion interchange is also responsible for the ImH and Hm chemical exchange. For the three NP2(V24E) ligand complexes, no EXSY cross peaks are observed, but the A:B ratios change dramatically with pH. The fact that heme favors the A orientation highly for NP2(V24E) at low pH as compared with wt NP2 is believed to be due to the steric effect of the V24E mutation. The existence of the B′ species at lower pH for wt NP2 complexes and the increase in A heme orientation at lower pH for NP2(V24E) are believed to be a result of a change in structure near Glu53 when it is protonated at low pH. ¹H{¹³C} heteronuclear multiple quantum coherence (HMQC) spectra are very helpful for the assignment of heme and nearby protein side chain resonances.     

Effects of acute doxorubicin treatment on hepatic proteome lysine acetylation status and the apoptotic environment

AIM: To determine if doxorubicin(Dox) alters hepatic proteome acetylation status and if acetylation status was associated with an apoptotic environment. METHODS: Doxorubicin(20 mg/kg; Sigma, Saint Louis, MO; n = 8) or NaCl(0.9%; n = 7) was administered as an intraperitoneal injection to male F344 rats, 6-wk of age. Once animals were treated with Dox or saline, all animals were fasted until sacrifice 24 h later. RESULTS: Dox treatment decreased proteome lysine acetylation likely due to a decrease in histone acetyltransferase activity. Proteome deacetylation may likely not be associated with a proapoptotic environment. Dox did not increase caspase-9,-8, or-3 activation nor poly(adenosine diphosphate-ribose) polymerase-1 cleavage. Dox did stimulate caspase-12 activation, however, it likely did not play a role in apoptosis induction. CONCLUSION: Early effects of Dox involve hepatic proteome lysine deacetylation and caspase-12 activa-tion under these experimental conditions.     

Habitat variables associated with encounters of Hottentot Buttonquail Turnix hottentottus during flush surveys across the Fynbos biome

The Hottentot Buttonquail Turnix hottentotus is an endangered terrestrial turnicid and is endemic to the Fynbos biome, South Africa. Due to its secretive nature and apparent rarity almost nothing is known about the species, but its range has been subject to anthropogenic modification, invasion by alien plant species and is vulnerable to climate change. To model covariates associated with the presence of Hottentot Buttonquail we undertook flush surveys across the Fynbos biome, covering 275 km. Habitat variables at encounter sites were recorded in vegetation plots, as well as locations without encounters. There was a critical number of observers needed during a flush survey in order to account for buttonquail presence, with no encounters with less than five participants. After accounting for this, we found probability of encounters decreased with increasing time-since-fire. Probability of encounters were also negatively associated with increasing percentage grass and other vegetation cover. We also found no association between percentage cover of Restionaceae plants and encounter probability, considered previously to be the best indicator of Hottentot Buttonquail presence. This information will be of use to those interested in managing habitat for this species and should inform future conservation efforts.