A Spectroscopic Description of Asymmetric Isotopologues of CO2.

A polyad-conserving algebraic model applied to vibrational excitations of asymmetric isotopologues of CO2 is presented. First, the problem of vibrational excitations is studied by taking into account only the minimum subspace of states to characterize the Fermi interaction. This analysis allows an estimation of the force constants as well as the feasibility of describing the system in a local mode scheme, in terms of SU(2) operators associated with Morse ladder operators for the stretches. This description together with the algebraic U(3) for the bends establishes the dynamical group SU1(2) × U(3) × SU2(2) for a series of isotopologues. Six isotopologues are considered, namely, 16O12C18O, 16O12C17O, 16O13C18O, 16O13C17O, 17O13C18O, and 17O12C18O in their electronic ground states. For isotopologues 16O12C18O, 16O12C17O, 17O12C18O, and 16O13C18O, the vibrational description was carried out using a Hamiltonian involving 14 parameters. For this series of isotopologues with a number of energy terms 90, 57, 42, and 40, the deviations obtained were rms = 0.15, 0.10, 0.06, and 0.07 cm-1, respectively. For 16O13C17O, with 28 experimental energies and involving 13 parameters, the deviation was rms = 0.05 cm-1, while for 17O13C18O, a different strategy was proposed since only 12 experimental energy levels. In all cases, the polyad scheme P212 = 2(ν1 + ν3) + ν2 was considered. In addition, a new criterion of locality/normality degree is proposed, embracing the case of molecules with normal mode behavior, in particular, the isotopologues of CO2.

Correction to: Ouabain Accelerates Collective Cell Migration Through a cSrc and ERK1/2 Sensitive Metalloproteinase Activity.

The original version of the article unfortunately contained an error in the author group. Dr. Isabel Larré was not submitted and published in the original version.

Ouabain Accelerates Collective Cell Migration Through a cSrc and ERK1/2 Sensitive Metalloproteinase Activity.

Studies made in the Madin-Darby canine kidney (MDCK) epithelial cell line showed that ouabain regulates cell adhesion and cell-adhesion-related biological processes, such as migration. Here, we demonstrated that 10 nM ouabain accelerates collective cell migration and heals wounds in cultured MDCK cell monolayers. Ouabain-induced acceleration of cell migration depends on activation of the cSrc-ERK1/2 signaling cascade, as it was inhibited by the kinase inhibitors PP2 and PD98059. Activation of the cSrc-ERK1/2 signaling cascade increased expression and activation of the extracellular matrix metalloproteinase-2 (MMP-2). Inhibition of MMP activity using the generic inhibitor GM6001 or the potent iMMP-2 inhibitor prevented the accelerative effect of ouabain. Likewise, Focal Adhesion Kinase (FAK) inhibition with the transfection of dominant negative peptide FRNK impaired the effect of ouabain. These results suggest that ouabain binding to the Na+,K+-ATPase accelerates collective migration of MDCK cells through activation of the cSrc-ERK1/2-FAK signaling cascade and promoting secretion and MMP activity.

Simulation of the Raman spectra of CO2: bridging the gap between algebraic models and experimental spectra.

The carbon dioxide Raman spectrum is simulated within an algebraic approach based on curvilinear coordinates in a local representation. The two main advantages of the present algebraic approach are a possible connection with configuration space and the correct description of systems with either local or normal mode character. The system Hamiltonian and polarizability tensor are expanded in terms of curvilinear coordinates. The curvilinear coordinates are in turn expanded into normal coordinates, obtaining an algebraic representation in terms of normal bosonic operators. A canonical transformation maps the operators into a local algebraic representation. The final step is an anharmonization procedure to local operators. The Raman spectrum of CO2 has been simulated, obtaining results close to experimental accuracy, and polarizability transition moments for the Raman spectral lines between 1150 cm(-1) and 1500 cm(-1) are reported. The comparison between experimental and simulated spectra has provided six new CO2 experimental vibrational terms.

Evisceración omental transanal posterior a lesión de recto / Omental evisceration through a rectal perforation: case report

Rectal perforation rarely occurs spontaneously. We report a 44 years old male consulting for abdominal pain lasting 12 hours. Abdominal muscular resistance was observed on physical examination. A plain abdominal X ray film showed a pneumoperitoneum. The patient was operated finding a perforation in the lower rectum, with omentum sliding through it and exiting through the anus. The omentum was sectioned and ligated and a derivative colostomy was performed. The cause of the rectal perforation was not ascertained.

La perforación de recto se produce como resultado de una complicación bajo condiciones patológicas que comprometen la pared rectal. Rara vez ocurre espontáneamente. En casi todos los casos reportados de lesión rectal asociada a evisceración intestinal, el intestino delgado es el órgano involucrado. Las técnicas de reparación son variables, desde una rafia primaria en lesiones poco extensas, hasta resección de segmento lesionado y colostomía para los casos más graves. La decisión de la técnica a utilizar dependerá de la extensión y otras características de la lesión, del compromiso de estructuras vecinas, del tiempo de evolución y del grado de contaminación. El cirujano general debe estar preparado para el manejo de estas lesiones ya que son de resolución en los servicios de urgencias. Presentamos un caso, poco frecuente, de evisceración del epiplón mayor, transanal, posterior a lesión rectal de dudosa etiología.

Afrontamiento primario con elásticos vasculares en el manejo del cierre progresivo de fasciotomías / Vessel loops for primary closure of fasciotomies

Background: Compartment syndrome of the extremity may occur after severe trauma with vascular lesions secondary to fractures, crushes or gunshots. To prevent it a fasciotomy must be done. Aim To report the use vessel loop shoelace technique for the progressive closure of the fasciotomy. Material and methods: Descnptive study of 24 patients aged 26 +/- 9 years (21 males) that required fasciotomy to prevent compartment syndromes. The fasciotomy wound was closed progressively using vessel loops anchored to the skin with staples or sutures, which were tightened progressively, according to the evolution. Results: The studied patients required a total of 56 fasciotomies. In all patients a complete or near complete closure of the wound was achieved. The mean closure time was 9.5 +/- 3.3 days. Mean hospital stay was 12.3 +/- 4.3 days. Conclusions: Vessel loop shoelace technique is effective for fasciotomy wound closure.

Frente al cada vez más frecuente manejo del trauma vascular en extremidades, debido a lesiones de distinta etiología, ya sea por accidentes de tránsito de alta velocidad, caídas de altura, o las crecientes tasas de lesiones en la vida civil por arma blanca y por arma de fuego, es que nos vemos enfrentados a múltiples tipos de lesiones vasculares que comprometen arterias y venas, asociados a extenso compromiso de partes blandas o a reintervenciones en períodos posteriores a las 6 hrs post trauma. De este modo es que el manejo asociado de la fasciotomía como método de prevención o tratamiento del síndrome compartamental es fundamental. Se presentan un total de 24 casos en los que se efectuaron 56 fasciotomías primarias o secundarias como profilaxis o tratamiento del síndrome compartamental, en las que se utilizaron elásticos vasculares para el cierre progresivo del defecto cutáneo de las fasciotomías, para disminuir el tiempo de evolución y así evitar el uso de injertos de piel en el cierre de los defectos.

Leiomyosarcoma of the vagina: case report and literature review.

Leiomyosarcoma of the vagina is quite rare. Extensive search of the literature discloses 137 case reports published over the past 40 years. Collectively, these reports give only cursory guidelines for diagnosis, management, and prognosis. We add another case to the sparse literature on leiomyosarcoma of the vagina. Treatment consisted of surgical excision. Tumor was found to extend to the margin of the excised specimen. The malignancy quickly recurred with lung metastases and the patient died. The very poor prognosis associated with this lesion emphasizes the critical need for early diagnosis and expeditious therapy. In the interest of improving salvage by prompt recognition and intervention, it is important for health-care professionals to be knowledgeable about and alert to this condition.

Herbaceous vegetation productivity, persistence, and metals uptake on a biosolids-amended mine soil.

The selection of plant species is critical for the successful establishment and long-term maintenance of vegetation on reclaimed surface mined soils. A study was conducted to assess the capability of 16 forage grass and legume species in monocultures and mixes to establish and thrive on a reclaimed Appalachian surface mine amended with biosolids. The 0.15-ha coarse-textured, rocky, non-acid forming mined site was prepared for planting by grading to a 2% slope and amending sandstone overburden materials with a mixture of composted and dewatered, anaerobically digested biosolids at a rate of 368 Mg ha(-1) (dry weight). Tall fescue (Festuca arundinacea Schreb.), orchardgrass (Dactylis glomerata L.), switchgrass (Panicum virgatum L.), caucasian bluestem (Bothriochloa caucasia L.), reed canarygrass (Phalaris arundinacea L.), ladino clover (Trifolium repens L.), birdsfoot trefoil (Lotus corniculatus L.), crownvetch (Coronilla varia L.), alfalfa (Medicago sativa L.), common sericea lespedeza and AULotan sericea lespedeza (Lespedeza cuneata L.), tall fescue-ladino clover, tall fescue-alfalfa, orchardgrass-birdsfoot trefoil, switchgrass-AULotan, and an herbaceous species mix intended for planting on reforested sites consisting of foxtail millet [Setaria italica (L.) Beauv.], perennial ryegrass (Lolium perenne L.), redtop (Agrostis alba L.), kobe lespedeza (Kummerowia striata L.), appalow lespedeza (Lespedeza cuneata L.), and birdsfoot trefoil were established between spring 1990 and 1991. Vegetative biomass and/or persistence were assessed in 1996, 1997, 1998, 2000, 2001, and 2002. The high rate of biosolids applied provided favorable soil chemical properties but could not overcome physical property limitations due to shallow undeveloped soil perched atop a compacted soil layer at 25 cm depth. The plant species whose persistence and biomass production were the greatest after a decade or more of establishment (i.e., switchgrass, sericea lespedeza, reed canarygrass, tall fescue, and crownvetch) shared the physiological and reproductive characteristics of low fertility requirements, drought and moisture tolerance, and propagation by rhizome and/or stolons. Of these five species, two (tall fescue and sericea lespedeza) are or have been seeded commonly on Appalachian coal surface mines, and often dominate abandoned pasture sites. Despite the high rates of heavy metal-bearing biosolids applied to the soil, plant uptake of Cd, Cu, Ni, and Zn were well within critical concentrations more than a decade after establishment of the vegetation.

Toxicologic evaluation of licorice extract as a cigarette ingredient.

Licorice extract (block, powder or liquid) may be applied to cigarette tobacco at levels of about 1-4% to enhance and harmonize the flavor characteristics of smoke, improve moisture holding characteristics of tobacco, and act as a surface active agent for ingredient application. Neat material pyrolysis studies, and smoke chemistry and biological activity studies (bacterial mutagenicity, cytotoxicity, micronucleus, and sub-chronic inhalation) with mainstream smoke, or mainstream smoke preparations from cigarettes containing various target levels (1.5-12%) of the licorice extracts were performed to provide data for an assessment of the use of licorice extract as a cigarette tobacco ingredient. At simulated tobacco burning temperatures up to 900 degrees C all forms of neat licorice extract pyrolyzed extensively, yielding small amounts of benzene, toluene, phenol and acetaldehyde with no indication that licorice extracts would transfer intact to mainstream smoke. As a single ingredient added to cigarette tobacco, block licorice extract at a target level of 12.5% increased smoke constituents including selected PAH, arsenic, lead, phenol and formaldehyde (on a TPM basis), while licorice extract powder (target level of 8% tobacco) increased select PAH, phenol and formaldehyde (on a TPM basis). Lower target application levels (including typical application levels) of block, powder or liquid licorice extract did not significantly alter the smoke chemistry profile. Biological tests indicated no relevant difference in the genotoxic or cytotoxic potential of either mainstream smoke (or smoke preparations) from cigarettes with added licorice extracts compared to control cigarettes. In sub-chronic 90-day rat inhalation studies, the mainstream smoke from cigarettes with 12.5% added block and 8% added powder licorice extract contained higher formaldehyde concentrations compared to control cigarette smoke. Female rats in the 12.5% block licorice extract exposure group displayed an increased incidence and severity of epithelial hyperplasia in the nose (level 2), with no relevant respiratory tract changes in the 8% powder licorice extract exposed rats. At the lower licorice extract application levels (1.25-5%), there was no indication of increased formaldehyde concentration in the smoke atmosphere and no relevant changes in respiratory tract tissues. Mineralcorticoid-like effects which have been associated with excess licorice ingestion were not found in any of the smoke inhalation studies. The results of these studies with various forms of licorice extract applied to cigarette tobacco suggest that adding licorice extract to cigarette tobacco at levels of < or =5% does not discernibly alter the smoke chemistry or biological effects normally associated with mainstream cigarette smoke.

Development of immunoassays for biomonitoring of hexamethylene diisocyanate exposure.

Hexamethylene diisocyanate (HDI) is used widely to manufacture polyurethanes for paints and coatings. It is an irritant and a chemical asthmagen. The U.S. Occupational Safety and Health Administration time-weighted average permissible exposure limit is 5 ppb and the ceiling limit is 20 ppb. We sought to develop a sensitive and specific immuno-bioassay to supplement workplace air monitoring and detect recent HDI exposure. For this, we produced rabbit antiserum to HDI-adducted keyhole limpet hemocyanin (HDI-KLH). The specificity of the antiserum was demonstrated by its reaction with a variety of HDI-conjugated proteins and the absence of reactions with conjugates of other diisocyanates, namely toluene diisocyanate and diphenyl methylene diisocyanate. Four immunoassays were developed and compared for their ability to detect decreasing quantities of HDI-adducted human serum albumin (HSA) containing 2 mol HDI adduct per mol HSA (HDI(2)-HSA) as determined by matrix-assisted laser desorption time-of-flight (MALDI-TOF) mass spectrometry. The sensitivities of some of the assays are within the range (0.82-45 nM) of current analytic methods. A Western analysis procedure has a sensitivity of 600 nM HDI adduct on HSA. ELISA inhibition assay, in which microtiter plates are coated with the HDI(2)-HSA antigen, has a sensitivity of 300 nM HDI adduct. An immunoblot assay has a sensitivity of 9 nM HDI adduct. The most sensitive bioassay (1.8 nM HDI adduct) is a three-antibody sandwich ELISA in which wells of microtiter plates are coated with the IgG fraction of the anti-HDI-KLH antisera. Compared with analytic methods for HDI biomonitoring, the immunoassays are faster and less costly and accommodate numerous samples simultaneously. The assays have the potential to affect industrial biomonitoring programs significantly.

Importance of inflammatory and immune components in a mouse model of airway reactivity to toluene diisocyanate (TDI).

BACKGROUND: Nearly 9 million individuals are exposed to agents in the workplace associated with asthma, and isocyanates represent the most common cause of occupationally induced asthma. OBJECTIVES: Nonetheless, the immunological mechanisms responsible for isocyanate-induced asthma are not clear. A murine model for toluene diisocyanate (TDI) asthma is described and employed to examine inflammatory and immune components that may be involved in the disease. METHODS: Groups (n = 6) of C57BL/6J and athymic mice were sensitized by subcutaneous injection (20 microl on day 1, 5 microl on days 4 and 11), and 7 days later challenged by inhalation (100 p.p.b., days 20, 22 and 24) with TDI. Twenty-four hours following the last challenge the tracheae and lungs were examined for histological changes as well as for the expression of Th1, Th2 and pro-inflammatory cytokines. Mice were also examined for airway reactivity to methacholine challenge and for specific and total IgE and IgG antibodies. RESULTS: TDI sensitization resulted in increased reactivity to methacholine challenge as well as a significant inflammatory response in the trachea and nares of wild-type mice, but not in the athymic mice nor in the lungs of the C57BL/6J mice. Airway inflammation was characterized by inflammatory cell influx, goblet cell metaplasia and epithelial damage. Histological changes in the trachea were accompanied by increased mRNA expression of interleukin (IL)-4, tumour necrosis factor alpha, lymphotoxin beta, lymphotactin and Rantes, as well as TDI-specific IgG antibodies and elevated levels of total IgE. IgE-specific antibodies were not detected with this exposure regimen but were produced when the TDI concentrations were increased. CONCLUSIONS: These studies provide a unique murine model for occupational asthma that generates both inflammatory and immune mediators similar to those occurring in TDI-induced asthma in humans.

Subclinical immunologic and physiologic responses in hexamethylene diisocyanate-exposed auto body shop workers.

BACKGROUND: Diisocyanates are potent sensitizing agents and currently the most commonly identified cause of occupational asthma in industrialized countries. However, diisocyanate asthma is difficult to diagnose and exposure and host risk factors are unclear. Auto body shops, one of the most common hexamethylene diisocyanate (HDI) exposure settings, are particularly difficult to study due to their small size and episodic exposures. Surveillance studies of such workers are limited. OBJECTIVES: We have initiated a cross-sectional field epidemiologic study, Survey of Painters and Repairers of Auto bodies by Yale (SPRAY), to characterize the effects of diisocyanate exposures on actively employed auto body shop workers. Methods and Results We present here questionnaire, physiologic, immunologic, and exposure data on 75 subjects enrolled in the study. No overt cases of clinically apparent diisocyanate asthma were identified based on spirometry, methacholine challenge, peak flows, and symptoms. HDI-specific lymphocyte proliferation was present in 30% of HDI-exposed workers and HDI-specific IgG in 34% of HDI-exposed workers, but they were not associated. HDI-specific IgE was detected in two workers. HDI-specific lymphocyte proliferation, increased methacholine responsiveness, and symptoms of chest tightness and shortness of breath were more common in the most heavily HDI-exposed workers, the painters. More long-term follow-up of this cohort should clarify the significance of these HDI-specific immunologic responses, physiologic changes, and symptoms. CONCLUSIONS: These findings demonstrate the presence of HDI-specific immune responses in a large proportion of healthy HDI-exposed workers.

Isolated airway exposure to toluene diisocyanate results in skin sensitization.

Toluene diisocyanate (TDI), a highly reactive industrial chemical is a leading cause of occupational asthma in westernized countries. It has also been reported to be a skin sensitizer in mice and guinea pigs although instances of skin sensitivity in humans are rare. It is uncertain if skin-contact is necessary to initiate the dermal sensitization. This study sought to determine if exclusive airway exposure to TDI could result in skin sensitivity. A group of guinea pigs was administered 50 microl of 0.6% TDI intratracheally (it.), another group received intranasal (in.) application of 0.6, 1.2, or 1.8% TDI. Eighty percent (4/5) of the it.-dosed animals, and 92% (11/12) of in.-dosed animals exhibited skin sensitivity. None of 14 control animals gave a positive reaction to patch challenge with TDI. These findings indicate that exclusive exposure of the airways to TDI can result in skin sensitivity and suggest that such events may be possible in TDI workers and should be considered in all workers exposed via the airways to chemical sensitizers.

Nifedipina microgránulos estudio multicéntrico abierto en pacientes con hipertensión arterial leve y moderada / Nifedipine microgranules study multicentric open and patients with hypertension arterial ligth and moderate

Se evaluó mediante un estudio multicéntrico prospectivo y abierto el efecto de la nifedipina en forma de microgránulos en el tratamiento de pacientes con hipertensión arterial leve y moderada. Fueron estudiados 67 pacientes, la administración de nifedipina microgránulos produjo un descenso del 17 por ciento en la presión arterial sistólica y del 23 por ciento en la presión arterial diastólica, se produjo además un descenso en la frecuencia del pulso que alcanzó significancia estadística. Los efectos adversos relacionados con la droga fueron poco frecuentes, consistieron en: cefalea, rubor y mareo de carácter leve que no ameritaron la suspensión del tratamiento

Rapid reduction of intracellular glutathione in human bronchial epithelial cells exposed to occupational levels of toluene diisocyanate.

Toluene diisocyanate (TDI) is a recognized chemical asthmogen, yet the mechanism of this toxicity and the molecular reactions involved have not been elucidated. We have previously shown that TDI vapor forms adducts with the apical surface of the respiratory epithelium, and that it colocalizes with ciliary tubulin. In vitro, we have shown rapid reaction of TDI with glutathione (GSH) and transfer of the bisGS-TDI adduct to a sulfhydryl-containing major histocompatibility complex peptide. This study sought to determine if intracellular GSH is altered following exposure to TDI. We used the dye CellTracker Green (chloromethylfluorescein, CMFDA) for detection of glutathione. One-day and 6-day air-liquid cultures of human bronchoepithelial cells (HBE) were exposed to 20-100 ppb TDI vapor for 5, 15, or 30 min. Cells were subsequently imaged using a confocal microscope. Both 1- and 6-day cultures showed a decrease in intensity of the thiol staining as a function of the TDI exposure dose. Doses as low as 20 ppb, the current permissible exposure limit (PEL) to TDI, resulted in rapid (within 5 min) decreases in fluorescence. The decreased fluorescence was not due to cytotoxicity or decrease in either esterase or glutathione-S-transferase activity, enzymes necessary for activation of the fluorescence of CMFDA. The decrease in glutathione levels was verified using another fluorescent label, ThioGlo(TM) 1, and cell extracts. In addition, the mucus produced by 6-day air-liquid interface HBE cells in response to TDI exposure appeared to be protective, as HBE cells underlying mucus retained more fluorescence than did cells in the same cultures that were not covered with mucus. These results, along with previous data, strongly suggest that TDI enters pulmonary cells and reacts rapidly with intracellular GSH, and that this can occur at the current PEL of 20 ppb. This rapid reaction suggests the importance of cellular thiols in TDI-induced pulmonary disease.

Comparison between phase space structures in coupled Morse systems and in various su(2) approximations.

While Hamiltonians written in terms of position and momentum provide a transparent picture of the motion of a system, Hamiltonians written in terms of Lie algebras are easier to handle quantum mechanically. Therefore we are interested to know how to transform one into the other. Since the exact transformation often leads to complicated expressions, we look for approximations which preserve the essential features. As basic criterion we look for the degree of equality of the classical phase space structures. We illustrate our ideas for the case of two coupled Morse systems and its approximation in terms of the Lie algebra su(2), which is relevant to anharmonic models of molecular spectroscopy. (c) 2001 American Institute of Physics.

Identification of human lung and skin proteins conjugated with hexamethylene diisocyanate in vitro and in vivo.

Diisocyanates are asthma-causing chemicals used in the commercial production of polyurethane. We have previously shown that human lung epithelial cell proteins can become conjugated with hexamethylene diisocyanate (HDI) and may be biologically important in diisocyanate-induced asthma. The objective of this study was to identify specific human lung and skin proteins that become conjugated with diisocyanate after in vitro and in vivo exposure. Following in vitro exposure of human airway epithelial cells (A549), keratin 18, the 78-kD glucose-regulated protein, trans-1, 2-dihyrobenzene-1,2-diol dehydrogenase, and actin were identified as prominent diisocyanate-conjugated proteins through use of a combination of immunocytochemical and mass spectrometric techniques. Following in vivo inhalation of an HDI aerosol, keratin 18 was also identified as the predominant diisocyanate-conjugated protein in human endobronchial biopsy samples, whereas albumin was the predominant diisocyanate-conjugated protein in bronchoalveolar lavage fluid. Keratin was also identified as a predominant diisocyanate-conjugated protein in human skin biopsy samples after epicutaneous exposure to liquid-phase HDI, although the major skin diisocyanate-conjugated protein (56-kD) differed from the predominant lung diisocyanate-conjugated keratin (47-kD). The data from this study identify keratin and other proteins as potential "carriers" for diisocyanates in vivo, and suggest that HDI conjugation of these proteins may play a role in the pathogenesis of diisocyanate-induced asthma.

Vibrational Excitations of Methane in the Framework of a Local-Mode Anharmonic Model.

The stretching and bending vibrations of methane are described in a local-mode anharmonic symmetry adapted model. Both Hecht- and Fermi-like interactions are considered. We start by establishing the Hamiltonian of the system in terms of internal coordinates and momenta. The Hamiltonian is then rewritten in terms of local creation (annihilation) operators a(dagger)(i)(a(i)), which are later anharmonized by means of the deformation of the harmonic oscillator algebra to the U(2) algebra. This procedure corresponds to the exact Morse result for the dominant matrix elements involved in the harmonically coupled anharmonic oscillator model (HCAO) introduced by Child and Lawton. We have carried out a fit to 40 experimental levels with an rms deviation of 1.17 cm(-1). In addition, we present a description of the dipole transition intensities. Copyright 2000 Academic Press.

TLA-1: a new plasmid-mediated extended-spectrum beta-lactamase from Escherichia coli.

Escherichia coli R170, isolated from the urine of an infected patient, was resistant to expanded-spectrum cephalosporins, aztreonam, ciprofloxacin, and ofloxacin but was susceptible to amikacin, cefotetan, and imipenem. This particular strain contained three different plasmids that encoded two beta-lactamases with pIs of 7.0 and 9.0. Resistance to cefotaxime, ceftazidime, aztreonam, trimethoprim, and sulfamethoxazole was transferred by conjugation from E. coli R170 to E. coli J53-2. The transferred plasmid, RZA92, which encoded a single beta-lactamase, was 150 kb in length. The cefotaxime resistance gene that encodes the TLA-1 beta-lactamase (pI 9.0) was cloned from the transconjugant by transformation to E. coli DH5alpha. Sequencing of the bla(TLA-1) gene revealed an open reading frame of 906 bp, which corresponded to 301 amino acid residues, including motifs common to class A beta-lactamases: (70)SXXK, (130)SDN, and (234)KTG. The amino acid sequence of TLA-1 shared 50% identity with the CME-1 chromosomal class A beta-lactamase from Chryseobacterium (Flavobacterium) meningosepticum; 48.8% identity with the VEB-1 class A beta-lactamase from E. coli; 40 to 42% identity with CblA of Bacteroides uniformis, PER-1 of Pseudomonas aeruginosa, and PER-2 of Salmonella typhimurium; and 39% identity with CepA of Bacteroides fragilis. The partially purified TLA-1 beta-lactamase had a molecular mass of 31.4 kDa and a pI of 9.0 and preferentially hydrolyzed cephaloridine, cefotaxime, cephalothin, benzylpenicillin, and ceftazidime. The enzyme was markedly inhibited by sulbactam, tazobactam, and clavulanic acid. TLA-1 is a new extended-spectrum beta-lactamase of Ambler class A.

Chlorpyrifos: an unwelcome pesticide in our homes.

Chlorpyrifos is an extensively used organophosphate insecticide having many urban and agricultural crop pest control uses. Studies conducted in indoor environments after termiticide, crack-and-crevice, broadcast, or fogger applications have shown that chlorpyrifos exposure can occur via inhalation of residual air concentrations, dermal or oral exposure from residues on floors and carpets, children toys, food, and dust. Not long ago the weight of scientific evidence supported safe indoor use, but recent studies support the possibility that when pregnant female rats are given the pesticide, chlorpyrifos causes brain damage in fetal rats. Moreover, the exposure of young rats to chlorpyrifos impairs early nervous system development. After finding that chlorpyrifos is an exposure risk especially to children, in June 2000 the United States Environmental Protection Agency and manufacturers agreed to voluntary measures that will reduce the exposure of children to chlorpyrifos-containing products. This action implies a search for less harmful new products to replace it and/or safer ways to control pests through basic hygiene. Whichever pest control method is selected, one should keep in mind that preventing environmental pesticide exposure in children is always better than treating the resulting disease.