In recent years, valuable experience and insights have been gained into L-forms (cell-wall-deficient variants) of bacteria and fungi and their disease-trigger potential in cases with chronic infections, autism spectru...In recent years, valuable experience and insights have been gained into L-forms (cell-wall-deficient variants) of bacteria and fungi and their disease-trigger potential in cases with chronic infections, autism spectrum disorders, autoimmune and neurodegenerative diseases. Based on the concept of “internal” blood microbiota, consisting of L-forms and its relevance to health and disease, the current study aims to outline the profile of dysbiotic disorders in three cancer patients (with endometrial cancer, breast cancer and acute myeloid leukemia), all in a phase before chemotherapy. Venous blood samples from the patients and from one control healthy person, were microbiologically studied. The used novel methodology of blood microbiota assessment was based on the following phases: isolation of L-forms, development and propagation, cultivation and conversion of L-forms into classical bacteria and fungi, as well as their identification with MALDI-TOF method. From the patients were isolated L-forms of opportunistic bacteria (Enterococcus faecalis, Esherichia coli, Enterobacter cloacae and Pseudomonas oryzihabitans) and fungi such as Rhodotorula mucilaginosa, Aspergillus fumigatus and Mucorales. In conclusion, the common feature found for the three cancer patients was the isolation from the blood of highly associated communities consisting of morphologically indistinguishable L-bodies, which through reversion in broth, were identified as distinct bacterial and fungal species. Unlike classic bacteria or fungi causing sepsis and bacteremia/fungemia, the presence of L-forms in blood is hidden, it does not demonstrate clinical signs nor it can be detected by conventional methods. It should be noted, however, that the dysbiotic blood microbiota shows unique and individual characteristics for the concrete cancer patient, correlates to the common state of the organism and tumor localization in the body, as well as it outlines the cancer promoting role of L-forms in processes of malignization, cancer genesis and progression.展开更多
<b><span style="font-family:Verdana;">Background</span></b><span style="font-family:""><span style="font-family:Verdana;">: The recognition of hum...<b><span style="font-family:Verdana;">Background</span></b><span style="font-family:""><span style="font-family:Verdana;">: The recognition of human blood microbiota, consisting of cell wall-deficient microbes (L-forms), is a major challenge today in the field of microbiology. There are accumulating data confirming the concept of “internal” blood L-form microbiota and its significance for health and diseases. Finding out whether the blood microbiota can be of diagnostic and prognostic importance for detection and evaluation of chronic infections anywhere in </span><span style="font-family:Verdana;">the body is a major objective. In the context of chronically infected upper</span> <span style="font-family:Verdana;">respiratory tract (URT), the aim of the current study was to understand</span><span style="font-family:Verdana;"> wheth</span><span style="font-family:Verdana;">er a local infection can be a source for entry of bacteria and fungi in th</span><span style="font-family:Verdana;">e blood. </span><b><span style="font-family:Verdana;">Methods: </span></b><span style="font-family:Verdana;">Blood samples from six persons with chronic inflammations</span><span style="font-family:Verdana;"> in URT diagnosed with hypertrophied adenoids, chronic sinusitis, nasal polyps, chronic naso-pharyngitis and one control healthy person were studied. Blood microbiota assessment methodology that be used, included three phases: </span></span><span style="font-family:Verdana;">1</span><span style="font-family:""><span style="font-family:Verdana;">) </span><span style="font-family:Verdana;">isolation of L-form cultures from blood-development and propagation;</span></span><span style="font-family:Verdana;">2</span><span style="font-family:""><span style="font-family:Verdana;">) cultivation directed to conversion of L-forms into bacterial and fungal cul</span><span style="font-family:Verdana;">tures;</span></span><span style="font-family:Verdana;">3</span><span style="font-family:Verdana;">) isolation of pure classical bacterial and fungal cultures and their</span><span style="font-family:""> <span><span style="font-family:Verdana;">identification by MALDI-TOF method. </span><b><span style="font-family:Verdana;">Results:</span></b><span style="font-family:Verdana;"> From the patients were isolated </span></span><span style="font-family:Verdana;">L-forms of opportunistic bacteria (</span><i><span style="font-family:Verdana;">Streptococcus mitis</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Roseomonas mucosa</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Dermacoccus nishinomiyaensis</span></i><span><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Enterococcus faecalis</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Acinetobacter johnsonii</span></i><span style="font-family:Verdana;">, </span></span><i><span style="font-family:Verdana;">Pseudomonas putida</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Staphylococcus aureus</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Pseudomonas luteola</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Enterobacter cloacae</span></i><span style="font-family:Verdana;">) and fungi such as </span><i><span style="font-family:Verdana;">Rhodotorula mucilaginosa</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Aspergillus niger</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Aspergillus fumigatus and Mucorales.</span></i> <b><span style="font-family:Verdana;">Conclusion:</span></b><span style="font-family:Verdana;"> The novel innovative methodology for assessment of blood L-form microbiota was successfully applied for detection of microbes responsible for chronic infections at URT.展开更多
Objective: To study the relationship between the polymorphism of drug resistant gene rpoB and drug resistance against rifampicin(RFP) of M. tuberculosis L-forms, and to evaluate its clinical application. Methods: A to...Objective: To study the relationship between the polymorphism of drug resistant gene rpoB and drug resistance against rifampicin(RFP) of M. tuberculosis L-forms, and to evaluate its clinical application. Methods: A total of 52 clinical isolated strains of M. tuberculosis L-forms were collected. rpoB gene polymorphism was analyzed by polymerase chain reaction and single-strand conformation polymorphism (PCR-SSCP) and conventional antimicrobial susceptibility test (AST). Their results were compared. Results: AST results showed that 38 of 52 clinical isolated strains were drug resistance (73.08%),while PCR-SSCP indicated 65.38% (32/52) rpoB gene polymorphism. There was no statistic significance(χ2= 2.4914) between the 2 methods. Conclusion:Combined the application of PCR-SSCP with AST in detecting rpoB drug resistant gene polymorphism of M. tuberculosis L-form from pneumoconiosis patients with tuberculosis may have advantages at earlier diagnosis and guidance of clinical medications.展开更多
Objective:To study the relationship between mutation in the katG gene and drug resistance of INH in Mycobacterium tuberculosis L-forms among patients of pneumoconiosis complicated with pulmonary tuberculosis, and to ...Objective:To study the relationship between mutation in the katG gene and drug resistance of INH in Mycobacterium tuberculosis L-forms among patients of pneumoconiosis complicated with pulmonary tuberculosis, and to explore the clinical application of PCR-SSCP. Methods: A total of 52 clinical isolated strains of Mycobacterium tuberculosis L-forms were collected. Mutation in the katG genes was detected by PCR-SSCP and traditional antimicrobial susceptibility test (AST). Results: The results by AST showed that there were 40 persisters in 52 clinical isolated strains. The drug resistant rate was 76.92%(40/52), and the gene mutation rate of katG was 57.70%(30/52)by PCR-SSCP, the difference was no quite significance (X^2 = 2.8507, P 〉 0.05). The coincidence rate of two methods was 75.00% (30/40). Conclusion: The detectionrate of katG resistant strains in Mycobacterium tuberculosis L-forms was high by PCR-SSCP. The combined application of PCR-SSCP and traditional antimicrobial susceptibility test can improve the detecting rate.展开更多
Objective: To study the relationship between drug resistant genetic mutation and drug resistance in Mycobacterium tuberculosis L-form, discuss the internal relationship between drug resistances and drug-resistant rel...Objective: To study the relationship between drug resistant genetic mutation and drug resistance in Mycobacterium tuberculosis L-form, discuss the internal relationship between drug resistances and drug-resistant related genes and explore the value of PCR- SSCP to clinical application. Methods: A total of 52 clinically isolated strains of tuberculosis L-form were collected among 97 pneumoconiosis patients complicated with tuberculosis. The gene mutations of katG, rpoB and rpsL were detected by PCR-SSCP, and the results were compared with those analyzed by traditional antimicrobial susceptibility test(AST). Results: The gene muta- tion rates of katG, rpoB and rpsL by PCR-SSCP were respectively 57.70% (30/52), 65.38% (32/52) and 40.38% (21/52). The rate of reversion was 78.85%(41/52) and the result of drag-resistant genes was invariable. The results of AST showed that there were 40 (76.92%) multi-drug resistant strains in 52 clinically isolated strains. The number for three-drug resistant strain was 21 (40.38%) and that of two-drug resistant was 19(36.54%), but only 12(23.08%) strains were one drug resistant. The rate of total drug-resistance was 100%, but there were 15 strains of allied mutation of three genes, 16 of two mutations and 6 of only one by PCR-SSCP. The coincidences were respectively 71.43%, 84.12% and 50.00%. Then there was no significant difference between the allied mutations of multi-drug resistant gene and the mutations of only one drug resistant gene (P 〉 0.05). Conclusion: PCR-SSCP technique has a higher sensibility and specificity to detect the genes of katG, rpoB and rpsL in tuberculosis L-form among pneumoconiosis complicated with tuberculosis,and the detecting rate of two drug resistant strains and three drug resistant strains was higher. The combined application of PCR-SSCP and AST has advantages at earlier diagnosis and guidance of clinical medications.展开更多
In this paper a zero-density estimate of the large sieve type is given for the automorphic L-function L f (s,χ),where f is a holomorphic cusp form and χ a Dirichlet character of mod q.
We discuss the equivalent form of the Ldvy-Leblond equation such that the nilpotent matrices are two-dimensional. We show that this equation can be obtained in the non-relativistic limit of the (2+1)-dimensional Di...We discuss the equivalent form of the Ldvy-Leblond equation such that the nilpotent matrices are two-dimensional. We show that this equation can be obtained in the non-relativistic limit of the (2+1)-dimensional Dirac equation. Phrthermore, we analyze the case with four-dimensional matrices, propose a Hamiltonian for the equation in (3+1) dimensions, and solve it for a Coulomb potential The quantized energy levels for the hydrogen atom are obtained, and the result is consistent with the non-relativistic quantum mechanics.展开更多
In this paper, we investigate the space of <em>L<sup>p</sup> p</em>-harmonic 1-forms on a complete noncompact orientable <em>δ</em>-stable hypersurface <em>M<sup>m</...In this paper, we investigate the space of <em>L<sup>p</sup> p</em>-harmonic 1-forms on a complete noncompact orientable <em>δ</em>-stable hypersurface <em>M<sup>m</sup></em> that is immersed in space form <img src="Edit_6fbc11b9-ac23-40e2-b045-0fb25419337d.png" width="35" height="23" alt="" /> with nonnegative BiRic curvature. We prove the nonexistence of <em>L<sup>p</sup> p</em>-harmonic 1-forms on <em>M<sup>m</sup></em>. Moreover, we obtain some vanishing properties for this class of harmonic 1-forms.展开更多
文摘In recent years, valuable experience and insights have been gained into L-forms (cell-wall-deficient variants) of bacteria and fungi and their disease-trigger potential in cases with chronic infections, autism spectrum disorders, autoimmune and neurodegenerative diseases. Based on the concept of “internal” blood microbiota, consisting of L-forms and its relevance to health and disease, the current study aims to outline the profile of dysbiotic disorders in three cancer patients (with endometrial cancer, breast cancer and acute myeloid leukemia), all in a phase before chemotherapy. Venous blood samples from the patients and from one control healthy person, were microbiologically studied. The used novel methodology of blood microbiota assessment was based on the following phases: isolation of L-forms, development and propagation, cultivation and conversion of L-forms into classical bacteria and fungi, as well as their identification with MALDI-TOF method. From the patients were isolated L-forms of opportunistic bacteria (Enterococcus faecalis, Esherichia coli, Enterobacter cloacae and Pseudomonas oryzihabitans) and fungi such as Rhodotorula mucilaginosa, Aspergillus fumigatus and Mucorales. In conclusion, the common feature found for the three cancer patients was the isolation from the blood of highly associated communities consisting of morphologically indistinguishable L-bodies, which through reversion in broth, were identified as distinct bacterial and fungal species. Unlike classic bacteria or fungi causing sepsis and bacteremia/fungemia, the presence of L-forms in blood is hidden, it does not demonstrate clinical signs nor it can be detected by conventional methods. It should be noted, however, that the dysbiotic blood microbiota shows unique and individual characteristics for the concrete cancer patient, correlates to the common state of the organism and tumor localization in the body, as well as it outlines the cancer promoting role of L-forms in processes of malignization, cancer genesis and progression.
文摘<b><span style="font-family:Verdana;">Background</span></b><span style="font-family:""><span style="font-family:Verdana;">: The recognition of human blood microbiota, consisting of cell wall-deficient microbes (L-forms), is a major challenge today in the field of microbiology. There are accumulating data confirming the concept of “internal” blood L-form microbiota and its significance for health and diseases. Finding out whether the blood microbiota can be of diagnostic and prognostic importance for detection and evaluation of chronic infections anywhere in </span><span style="font-family:Verdana;">the body is a major objective. In the context of chronically infected upper</span> <span style="font-family:Verdana;">respiratory tract (URT), the aim of the current study was to understand</span><span style="font-family:Verdana;"> wheth</span><span style="font-family:Verdana;">er a local infection can be a source for entry of bacteria and fungi in th</span><span style="font-family:Verdana;">e blood. </span><b><span style="font-family:Verdana;">Methods: </span></b><span style="font-family:Verdana;">Blood samples from six persons with chronic inflammations</span><span style="font-family:Verdana;"> in URT diagnosed with hypertrophied adenoids, chronic sinusitis, nasal polyps, chronic naso-pharyngitis and one control healthy person were studied. Blood microbiota assessment methodology that be used, included three phases: </span></span><span style="font-family:Verdana;">1</span><span style="font-family:""><span style="font-family:Verdana;">) </span><span style="font-family:Verdana;">isolation of L-form cultures from blood-development and propagation;</span></span><span style="font-family:Verdana;">2</span><span style="font-family:""><span style="font-family:Verdana;">) cultivation directed to conversion of L-forms into bacterial and fungal cul</span><span style="font-family:Verdana;">tures;</span></span><span style="font-family:Verdana;">3</span><span style="font-family:Verdana;">) isolation of pure classical bacterial and fungal cultures and their</span><span style="font-family:""> <span><span style="font-family:Verdana;">identification by MALDI-TOF method. </span><b><span style="font-family:Verdana;">Results:</span></b><span style="font-family:Verdana;"> From the patients were isolated </span></span><span style="font-family:Verdana;">L-forms of opportunistic bacteria (</span><i><span style="font-family:Verdana;">Streptococcus mitis</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Roseomonas mucosa</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Dermacoccus nishinomiyaensis</span></i><span><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Enterococcus faecalis</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Acinetobacter johnsonii</span></i><span style="font-family:Verdana;">, </span></span><i><span style="font-family:Verdana;">Pseudomonas putida</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Staphylococcus aureus</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Pseudomonas luteola</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Enterobacter cloacae</span></i><span style="font-family:Verdana;">) and fungi such as </span><i><span style="font-family:Verdana;">Rhodotorula mucilaginosa</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Aspergillus niger</span></i><span style="font-family:Verdana;">,</span><i><span style="font-family:Verdana;"> Aspergillus fumigatus and Mucorales.</span></i> <b><span style="font-family:Verdana;">Conclusion:</span></b><span style="font-family:Verdana;"> The novel innovative methodology for assessment of blood L-form microbiota was successfully applied for detection of microbes responsible for chronic infections at URT.
文摘Objective: To study the relationship between the polymorphism of drug resistant gene rpoB and drug resistance against rifampicin(RFP) of M. tuberculosis L-forms, and to evaluate its clinical application. Methods: A total of 52 clinical isolated strains of M. tuberculosis L-forms were collected. rpoB gene polymorphism was analyzed by polymerase chain reaction and single-strand conformation polymorphism (PCR-SSCP) and conventional antimicrobial susceptibility test (AST). Their results were compared. Results: AST results showed that 38 of 52 clinical isolated strains were drug resistance (73.08%),while PCR-SSCP indicated 65.38% (32/52) rpoB gene polymorphism. There was no statistic significance(χ2= 2.4914) between the 2 methods. Conclusion:Combined the application of PCR-SSCP with AST in detecting rpoB drug resistant gene polymorphism of M. tuberculosis L-form from pneumoconiosis patients with tuberculosis may have advantages at earlier diagnosis and guidance of clinical medications.
基金National Science Foundation Youth fund of Anhui University of Science & Technology(200537)
文摘Objective:To study the relationship between mutation in the katG gene and drug resistance of INH in Mycobacterium tuberculosis L-forms among patients of pneumoconiosis complicated with pulmonary tuberculosis, and to explore the clinical application of PCR-SSCP. Methods: A total of 52 clinical isolated strains of Mycobacterium tuberculosis L-forms were collected. Mutation in the katG genes was detected by PCR-SSCP and traditional antimicrobial susceptibility test (AST). Results: The results by AST showed that there were 40 persisters in 52 clinical isolated strains. The drug resistant rate was 76.92%(40/52), and the gene mutation rate of katG was 57.70%(30/52)by PCR-SSCP, the difference was no quite significance (X^2 = 2.8507, P 〉 0.05). The coincidence rate of two methods was 75.00% (30/40). Conclusion: The detectionrate of katG resistant strains in Mycobacterium tuberculosis L-forms was high by PCR-SSCP. The combined application of PCR-SSCP and traditional antimicrobial susceptibility test can improve the detecting rate.
基金This work was supported by the Youth Natural Science Foundation of Anhui University of Science & Technology(200537)
文摘Objective: To study the relationship between drug resistant genetic mutation and drug resistance in Mycobacterium tuberculosis L-form, discuss the internal relationship between drug resistances and drug-resistant related genes and explore the value of PCR- SSCP to clinical application. Methods: A total of 52 clinically isolated strains of tuberculosis L-form were collected among 97 pneumoconiosis patients complicated with tuberculosis. The gene mutations of katG, rpoB and rpsL were detected by PCR-SSCP, and the results were compared with those analyzed by traditional antimicrobial susceptibility test(AST). Results: The gene muta- tion rates of katG, rpoB and rpsL by PCR-SSCP were respectively 57.70% (30/52), 65.38% (32/52) and 40.38% (21/52). The rate of reversion was 78.85%(41/52) and the result of drag-resistant genes was invariable. The results of AST showed that there were 40 (76.92%) multi-drug resistant strains in 52 clinically isolated strains. The number for three-drug resistant strain was 21 (40.38%) and that of two-drug resistant was 19(36.54%), but only 12(23.08%) strains were one drug resistant. The rate of total drug-resistance was 100%, but there were 15 strains of allied mutation of three genes, 16 of two mutations and 6 of only one by PCR-SSCP. The coincidences were respectively 71.43%, 84.12% and 50.00%. Then there was no significant difference between the allied mutations of multi-drug resistant gene and the mutations of only one drug resistant gene (P 〉 0.05). Conclusion: PCR-SSCP technique has a higher sensibility and specificity to detect the genes of katG, rpoB and rpsL in tuberculosis L-form among pneumoconiosis complicated with tuberculosis,and the detecting rate of two drug resistant strains and three drug resistant strains was higher. The combined application of PCR-SSCP and AST has advantages at earlier diagnosis and guidance of clinical medications.
基金Supported by the NNSF of China(11071186)Supported by the Science Foundation for the Excellent Youth Scholars of Shanghai(ssc08017)Supported by the Doctoral Research Fund of Shanghai Ocean University
文摘In this paper a zero-density estimate of the large sieve type is given for the automorphic L-function L f (s,χ),where f is a holomorphic cusp form and χ a Dirichlet character of mod q.
文摘We discuss the equivalent form of the Ldvy-Leblond equation such that the nilpotent matrices are two-dimensional. We show that this equation can be obtained in the non-relativistic limit of the (2+1)-dimensional Dirac equation. Phrthermore, we analyze the case with four-dimensional matrices, propose a Hamiltonian for the equation in (3+1) dimensions, and solve it for a Coulomb potential The quantized energy levels for the hydrogen atom are obtained, and the result is consistent with the non-relativistic quantum mechanics.
文摘In this paper, we investigate the space of <em>L<sup>p</sup> p</em>-harmonic 1-forms on a complete noncompact orientable <em>δ</em>-stable hypersurface <em>M<sup>m</sup></em> that is immersed in space form <img src="Edit_6fbc11b9-ac23-40e2-b045-0fb25419337d.png" width="35" height="23" alt="" /> with nonnegative BiRic curvature. We prove the nonexistence of <em>L<sup>p</sup> p</em>-harmonic 1-forms on <em>M<sup>m</sup></em>. Moreover, we obtain some vanishing properties for this class of harmonic 1-forms.