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1.
Water Res ; 116: 65-75, 2017 06 01.
Article in English | MEDLINE | ID: mdl-28314209

ABSTRACT

Hospital wastewaters are a main source of pharmaceutical active compounds, which are usually highly recalcitrant and can accumulate in surface and groundwater bodies. Fungal treatments can remove these contaminants prior to discharge, but real wastewater poses a problem to fungal survival due to bacterial competition. This study successfully treated real non-spiked, non-sterile wastewater in a continuous fungal fluidized bed bioreactor coupled to a coagulation-flocculation pretreatment for 56 days. A control bioreactor without the fungus was also operated and the results were compared. A denaturing gradient gel electrophoresis (DGGE) and sequencing approach was used to study the microbial community arisen in both reactors and as a result some bacterial degraders are proposed. The fungal operation successfully removed analgesics and anti-inflammatories, and even the most recalcitrant pharmaceutical families such as antibiotics and psychiatric drugs.


Subject(s)
Flocculation , Wastewater , Bioreactors/microbiology , Fungi , Hospitals , Pharmaceutical Preparations , Waste Disposal, Fluid
2.
J Hazard Mater ; 318: 561-570, 2016 Nov 15.
Article in English | MEDLINE | ID: mdl-27469044

ABSTRACT

Hospital wastewaters have a high load of pharmaceutical active compounds (PhACs). Fungal treatments could be appropriate for source treatment of such effluents but the transition to non-sterile conditions proved to be difficult due to competition with indigenous microorganisms, resulting in very short-duration operations. In this article, coagulation-flocculation and UV-radiation processes were studied as pretreatments to a fungal reactor treating non-sterile hospital wastewater in sequential batch operation and continuous operation modes. The influent was spiked with ibuprofen and ketoprofen, and both compounds were successfully degraded by over 80%. UV pretreatment did not extent the fungal activity after coagulation-flocculation measured as laccase production and pellet integrity. Sequential batch operation did not reduce bacteria competition during fungal treatment. The best strategy was the addition of a coagulation-flocculation pretreatment to a continuous reactor, which led to an operation of 28days without biomass renovation.


Subject(s)
Medical Waste Disposal/methods , Medical Waste , Trametes/metabolism , Waste Disposal, Fluid/methods , Biomass , Bioreactors , Hospitals , Ibuprofen/chemistry , Ibuprofen/metabolism , Ketoprofen/chemistry , Ketoprofen/metabolism , Laccase/biosynthesis , Ultraviolet Rays , Water Microbiology , Water Pollutants, Chemical
3.
Theriogenology ; 85(7): 1343-7, 2016 Apr 15.
Article in English | MEDLINE | ID: mdl-26786244

ABSTRACT

This study examines the possible effects of progesterone (P4) supplementation during the time of pregnancy recognition, from Days 15 to 17 post-artificial insemination (AI), on reproductive performance in high-producing dairy cows. Cows in their 15th day post-AI were alternately assigned to a control, no-treatment group (C: n = 257) or treatment group (P4: n = 287) on a weekly rotational basis according to the chronologic order of their gynecologic visit. On the basis of the odds ratio, the interaction treatment × previous placenta retention had a significant effect (P = 0.02) on conception rate. Thus, cows in P4 that had not suffered a retained placenta were 1.6 times more likely to conceive 28 to 34 days post-AI than the remaining cows. In nonpregnant cows, treatment had no effect on subsequent return to estrus or AI interval and neither were any effects of treatment observed on twin pregnancy and early fetal loss rates. The results of this study demonstrate the efficacy of P4 supplementations during the time of pregnancy recognition after AI in cows without a clinical history of placenta retention.


Subject(s)
Cattle/physiology , Fertilization/drug effects , Insemination, Artificial/veterinary , Progesterone/pharmacology , Progestins/pharmacology , Animals , Female , Odds Ratio , Pregnancy , Progesterone/administration & dosage , Progestins/administration & dosage
4.
Reprod Domest Anim ; 49(4): 529-535, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24888579

ABSTRACT

Q fever is a zoonosis produced by Coxiella burnetii, a bacterium that is widely distributed worldwide. Domestic ruminants are the most important source of C. burnetii for human infection. In sheep and goats, abortion is the main clinical consequence of infection, yet the symptoms described in cattle have so far been inconsistent. Q fever has been also scarcely reported in cattle, most likely because of its difficult diagnosis at the farm level and because of the many existing responsible C. burnetii strains. In this report, the effects of C. burnetii infection or Q fever disease on the reproductive behaviour of dairy cattle are reviewed, with special emphasis placed on the scarcity of data available and possible control actions discussed.


Subject(s)
Pregnancy Complications, Infectious/veterinary , Q Fever/veterinary , Reproduction , Abortion, Veterinary/microbiology , Animals , Animals, Newborn , Antibodies, Bacterial/blood , Bacterial Vaccines , Cattle , Cattle Diseases , Coxiella burnetii/immunology , Female , Fetal Diseases/microbiology , Fetal Diseases/veterinary , Goat Diseases/microbiology , Goats , Humans , Infertility, Female/microbiology , Infertility, Female/prevention & control , Infertility, Female/veterinary , Pregnancy , Pregnancy Complications, Infectious/microbiology , Puerperal Infection/microbiology , Puerperal Infection/veterinary , Q Fever/complications , Q Fever/diagnosis , Q Fever/prevention & control , Sheep/microbiology , Sheep Diseases
5.
Vaccine ; 31(30): 3046-50, 2013 Jun 26.
Article in English | MEDLINE | ID: mdl-23692696

ABSTRACT

This study was designed to assess the safety of phase I vaccination against Coxiella burnetii in advanced pregnancy and the effect of vaccination on subsequent reproductive performance of high producing dairy cows. C. burnetii serostatus was determined in 719 dairy cows by individual serological testing. According to their serostatus, cows were randomly assigned to a control (n=359) or vaccine (n=360) group (inactivated phase I on Days 171-177 and 192-198 of gestation, Coxevac-Ceva Sante Animale). Using a χ(2)-test, vaccination had no effect on abortion before parturition, retention of placenta and stillbirth, either in seropositive as in seronegative cows. Cox's proportional hazards model revealed that cows in the vaccine group were 1.22 times more likely to conceive during the first 150 days in milk than cows in the control group. Moreover, the likelihood of pregnancy was lower in multiparous cows, cows with a retained placenta and cows undergoing first AI during the warm season compared to the remaining animals (by factors of 0.75, 0.69 and 0.69, respectively). In animals testing seronegative for C. burnetii, the likelihood of pregnancy was 1.25 times higher in vaccinated cows compared to non-vaccinated seronegative animals. No effect of vaccination on subsequent fertility was detected in seropositive animals. In conclusion, the results of this study indicate that phase I vaccination against C. burnetii during advanced pregnancy in dairy cows is safe and improves subsequent fertility of C. burnetii seronegative animals.


Subject(s)
Bacterial Vaccines/administration & dosage , Cattle Diseases/prevention & control , Pregnancy, Animal/immunology , Q Fever/veterinary , Vaccination/veterinary , Animals , Bacterial Vaccines/adverse effects , Cattle , Cattle Diseases/immunology , Coxiella burnetii/immunology , Female , Humans , Lactation , Milk , Pregnancy , Q Fever/immunology , Q Fever/prevention & control , Serologic Tests , Vaccination/adverse effects
6.
Leukemia ; 27(11): 2157-64, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23584566

ABSTRACT

We retrospectively assessed whether normalized bone marrow WT1 levels could be used for risk stratification in a consecutive series of 584 acute myeloid leukemia (AML) patients. A cutoff value of 5065 copies at diagnosis identified two prognostic groups (overall survival (OS): 44 ± 3 vs 36 ± 3%, P=0.023; leukemia-free survival (LFS): 47 ± 3 vs 36 ± 4%, P=0.038; and cumulative incidence of relapse (CIR): 37 ± 3 vs 47 ± 4%, P=:0.043). Three groups were identified on the basis of WT1 levels post-induction: Group 0 (WT1 between 0 and 17.5 copies, 134 patients, OS: 59 ± 4%, LFS:59 ± 4% and CIR: 26 ± 4%); Group 1 (WT1 between 17.6 and 170.5 copies, 160 patients, OS: 48 ± 5%, LFS:41 ± 4% and CIR: 45 ± 4%); and Group 2 (WT1 >170.5 copies, 71 patients, OS: 23 ± 6%, LFS: 19 ± 7% and CIR: 68 ± 8%) (P<0.001). Post-intensification samples distinguished three groups: patients with WT1 >100 copies (47 patients, 16%); an intermediate group of patients with WT1 between 10 and 100 copies (148 patients, 52%); and a third group with WT1 <10 copies (92 patients, 32%). Outcomes differed significantly in terms of OS (30 ± 7%, 59 ± 4%, 72 ± 5%), LFS (24 ± 7%, 46 ± 4%, 65 ± 5%) and relapse probability (CIR 72 ± 7%, 45 ± 4%, 25 ± 5%), all P<0.001. WT1 levels in bone marrow assayed using the standardized ELN method provide relevant prognostic information in de novo AML.


Subject(s)
Antineoplastic Agents/therapeutic use , Biomarkers, Tumor/genetics , Bone Marrow/metabolism , Neoplasm Recurrence, Local/genetics , Neoplasm, Residual/genetics , WT1 Proteins/genetics , Adolescent , Adult , Aged , Biomarkers, Tumor/metabolism , Bone Marrow/drug effects , Bone Marrow/pathology , Consolidation Chemotherapy , Female , Follow-Up Studies , Gene Dosage , Humans , Immunophenotyping , Leukemia, Myeloid, Acute , Male , Middle Aged , Neoplasm Recurrence, Local/diagnosis , Neoplasm Recurrence, Local/drug therapy , Neoplasm Recurrence, Local/mortality , Neoplasm Staging , Neoplasm, Residual/diagnosis , Neoplasm, Residual/drug therapy , Neoplasm, Residual/mortality , Polymerase Chain Reaction , Prognosis , Remission Induction , Retrospective Studies , Survival Rate , WT1 Proteins/metabolism , Young Adult
7.
Reprod Domest Anim ; 48(3): 441-6, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23106514

ABSTRACT

The objective of this study was to assess the effects of Coxiella burnetii shedding or seropositivity on post-partum recovery and subsequent fertility in high-producing dairy cows. Given the difficulty in diagnosing C. burnetii infection at the farm level, an exhaustive series of tests in 43 pregnant animals that delivered at least one live calf were conducted, including blood serology and PCR of milk or colostrum, cotyledons (only at parturition), faeces, vaginal fluid against C. burnetii on gestation Day 171-177, at parturition and on Days 1-7, 8-14, 15-21, 22-28, 29-35 and 90-97 post-partum. During scheduled herd visits, ultrasonography (US) of the genital tract and examination of vaginal fluid were performed on Days 15-21 (V1), 22-28 (V2), 29-35 (V3) and 51-57 (V4) post-partum by the same veterinarian. Logistic regression analysis revealed that the likelihood of suffering endometritis (the presence of echogenic intrauterine fluid (IUF), cervical diameter of ≥4 cm or endometrial thickness ≥0.75 cm) was lower in C. burnetii-seropositive animals (OR = 0.10), compared with C. burnetii-seronegative animals. According to Kaplan-Meier survival analysis, C. burnetii-seronegative and non-shedding cows showed a delayed return to luteal activity and conception was delayed in non-shedding animals, compared with the remaining animals. Overall, the results of our study provide useful insight into the effects of C. burnetii infection on post-partum recovery and subsequent fertility. In particular, animals not infected with Coxiella seem to be susceptible to infection and not protected against the bacterium in dairy herds. The elevated costs of determining an infection at the farm level, make monitoring of cows virtually impossible from a clinical point of view.


Subject(s)
Bacterial Shedding/physiology , Cattle Diseases/microbiology , Coxiella burnetii/isolation & purification , Q Fever/veterinary , Animals , Antibodies, Bacterial/blood , Cattle , Female , Peripartum Period , Pregnancy , Proportional Hazards Models , Q Fever/microbiology
10.
Eur J Haematol ; 41(4): 317-20, 1988 Oct.
Article in English | MEDLINE | ID: mdl-3197819

ABSTRACT

Plasma-cholesterol concentrations were determined in 85 acute myelogenous leukemia patients. Measurements were repeated in 28 cases during remission. Mean plasma-cholesterol concentration (+/- SD) at diagnosis was 3.95 mmol/l (+/- 1.29). 47 patients (55.3%) had hypocholesterolemia (less than 3.87 mmol/l). Among the main clinical, hematologic and biochemical parameters, only high leukocyte counts were correlated with hypocholesterolemia. As far the FAB subtypes are concerned, the lowest cholesterol levels were observed in leukemias with monocytic component. However, although the same FAB subtypes showed significantly higher leucocytes counts than the other subtypes, both parameters were independently related to low cholesterol levels. Remission was associated with a significant increase in cholesterol levels in those patients with low cholesterol concentrations or high leukocyte counts at diagnosis. These results support the idea that initial hypocholesterolemia in acute myelogenous leukemia is related to the tumoral mass present at diagnosis.


Subject(s)
Cholesterol/blood , Dyslipidemias/etiology , Leukemia, Myeloid, Acute/blood , Adult , Aged , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Female , Humans , Leukemia, Myeloid, Acute/classification , Leukemia, Myeloid, Acute/complications , Leukemia, Myeloid, Acute/drug therapy , Leukocyte Count , Male , Middle Aged
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