Francisco J Flores-Tena, Alma L Guerrero-Barrera, Francisco J Avelar-González, E Marcela Ramírez-López, M Consolación Martínez-Saldaña
The occurrence of Gram-negative pathogenic and opportunistic species, was studied for two years on air. soil and leachate from the San Nicolás Landfill. Aguascalientes, Mexico. For soil and leachate four samplings were done, two during the dry season and two during the rainy season. For soil there were 15 sampling points, the leachate samples were taken on the leachate tank. For air, twelve sampling were done in three points of the landfill. Twenty pathogenic and/or opportunistic bacteria were identified from air, twenty from soil and eleven from leachate. Most of them were enteric; however respiratory tract pathogenic bacteria were also identified. Pasteurella haemolytica were isolated in all air samples. Nine species were found in the a half of the soil samples. The most frequent species in leachate were Acinetobacter baumanii, Bordetella sp, Brucella sp. and Escherichia coli var II. The occurrence of pathogenic and opportunistic species points out to the nosocomial and domestic clinical wastes discharged in the landfill as a potential risk for public and occupational health.
{"title":"Pathogenic and opportunistic gram-negative bacteria in soil, leachate and air in San Nicolás landfill at Aguascalientes, Mexico.","authors":"Francisco J Flores-Tena, Alma L Guerrero-Barrera, Francisco J Avelar-González, E Marcela Ramírez-López, M Consolación Martínez-Saldaña","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The occurrence of Gram-negative pathogenic and opportunistic species, was studied for two years on air. soil and leachate from the San Nicolás Landfill. Aguascalientes, Mexico. For soil and leachate four samplings were done, two during the dry season and two during the rainy season. For soil there were 15 sampling points, the leachate samples were taken on the leachate tank. For air, twelve sampling were done in three points of the landfill. Twenty pathogenic and/or opportunistic bacteria were identified from air, twenty from soil and eleven from leachate. Most of them were enteric; however respiratory tract pathogenic bacteria were also identified. Pasteurella haemolytica were isolated in all air samples. Nine species were found in the a half of the soil samples. The most frequent species in leachate were Acinetobacter baumanii, Bordetella sp, Brucella sp. and Escherichia coli var II. The occurrence of pathogenic and opportunistic species points out to the nosocomial and domestic clinical wastes discharged in the landfill as a potential risk for public and occupational health.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"49 1-2","pages":"25-30"},"PeriodicalIF":0.0,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27589385","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
In Mexico, zero tolerance regulation is practiced regarding Salmonella in food products. the presence of which is verified by the procedure described in NOM 114-SSA-1994. During the period between August 2002 and March 2003, 245 food samples were tested using this procedure in the Central Laboratories of the Department of Health for the State of Jalisco (CEESLAB). Of these 245 samples, 35 showed presumptive colonies contaminated with Proteus swarm cells even after selective isolation. These swarm cells make Salmonella recovery and biochemical identification difficult due to the occurance of atypical biochemical profiles which generally correspond to that of Proteus. Out of the 35 samples contaminated with Proteus, 65 presumptive colonies were isolated. These colonies were analyzed using both normative microbiological method and Polymerase Chain Reaction (PCR). The PCR method detected two positive samples while normative microbiological method was not able to identify. In order to determine the extent of interference of Proteus swarming on the Salmonella-specific PCR band amplification, Salmonella ser. Typhimurium was grown in the presence of Proteus swarming. These results show that Proteus swarming did not interfere with Salmonella PCR-amplification, although the appearance of Sanlmonella was altered such that the black precipitate was no observed in the presence of Proteus swarming. Ours result indicate that the PCR method used in this study may be successfully applied to confirm presumptive Salmnonella colonies contaminated with Proteus swarming.
{"title":"Confirmation of presumptive Salmonella colonies contaminated with Proteus swarming using the polymerase chain reaction (PCR) method.","authors":"Rosalba Gutiérrez Rojo, Edith Torres Chavolla","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>In Mexico, zero tolerance regulation is practiced regarding Salmonella in food products. the presence of which is verified by the procedure described in NOM 114-SSA-1994. During the period between August 2002 and March 2003, 245 food samples were tested using this procedure in the Central Laboratories of the Department of Health for the State of Jalisco (CEESLAB). Of these 245 samples, 35 showed presumptive colonies contaminated with Proteus swarm cells even after selective isolation. These swarm cells make Salmonella recovery and biochemical identification difficult due to the occurance of atypical biochemical profiles which generally correspond to that of Proteus. Out of the 35 samples contaminated with Proteus, 65 presumptive colonies were isolated. These colonies were analyzed using both normative microbiological method and Polymerase Chain Reaction (PCR). The PCR method detected two positive samples while normative microbiological method was not able to identify. In order to determine the extent of interference of Proteus swarming on the Salmonella-specific PCR band amplification, Salmonella ser. Typhimurium was grown in the presence of Proteus swarming. These results show that Proteus swarming did not interfere with Salmonella PCR-amplification, although the appearance of Sanlmonella was altered such that the black precipitate was no observed in the presence of Proteus swarming. Ours result indicate that the PCR method used in this study may be successfully applied to confirm presumptive Salmnonella colonies contaminated with Proteus swarming.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"49 1-2","pages":"19-24"},"PeriodicalIF":0.0,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27589473","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Suero costeño is a fermented milk product from the Colombian Atlantic coast, which is produced by the spontaneous acidification of raw milk due to the action of environmental microbes during traditional and semi-industrial processes. Eleven fermentations were carried out in experimental settings replicating traditional conditions and changes in concentration among microbial groups involved during the process (Aerobic Mesophilic bacteria, Yeasts, Enterobacteriaceae and Lactic Acid Bacteria (LAB)). LAB plays an important role in the fermentation process, especially during the final stage (24 hours). In addition, yeasts seem to have an effect on fermentation, showing an increase during the first hours of the process, while Enterobacterial counts decreased during fermentation. Thirty six LAB strains were isolated from commercial samples and thirty two were identified using the API 50 CH kit (BioMCrieux). 41% of the strains identified belonged to the species Lb. plantarum, and 19% were Lb. paracasei subsp. paracasei. Sugars fermented by LAB include milk carbohydrates such as D-Lactose, D-Glucose and D-Galactose. Because of their capacity to use other carbohydrates (manose, celobiose, maltose, fructose, ribose, trehalose, salicin, gentiobiose), it would also be possible to use these strains as starter cultures for other fermentations.
{"title":"Preliminary studies on the microbiological characterization of lactic acid bacteria in suero costeño, a Colombian traditional fermented milk product.","authors":"C Cueto, D García, F Garcés, J Cruz","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Suero costeño is a fermented milk product from the Colombian Atlantic coast, which is produced by the spontaneous acidification of raw milk due to the action of environmental microbes during traditional and semi-industrial processes. Eleven fermentations were carried out in experimental settings replicating traditional conditions and changes in concentration among microbial groups involved during the process (Aerobic Mesophilic bacteria, Yeasts, Enterobacteriaceae and Lactic Acid Bacteria (LAB)). LAB plays an important role in the fermentation process, especially during the final stage (24 hours). In addition, yeasts seem to have an effect on fermentation, showing an increase during the first hours of the process, while Enterobacterial counts decreased during fermentation. Thirty six LAB strains were isolated from commercial samples and thirty two were identified using the API 50 CH kit (BioMCrieux). 41% of the strains identified belonged to the species Lb. plantarum, and 19% were Lb. paracasei subsp. paracasei. Sugars fermented by LAB include milk carbohydrates such as D-Lactose, D-Glucose and D-Galactose. Because of their capacity to use other carbohydrates (manose, celobiose, maltose, fructose, ribose, trehalose, salicin, gentiobiose), it would also be possible to use these strains as starter cultures for other fermentations.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"49 1-2","pages":"12-8"},"PeriodicalIF":0.0,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27589471","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marisol Blancas Mosqueda, Rafael Herrera Esparza, Cristina Rodríguez Padilla, Jesús Patricio Tavizón García, Marisa Mercado Reyes, Valentin Badillo Almaraz, Francisco Echavarría, Adrián López Saucedo, Carmen Mondragón de la Peña
We developed an experimental model of hydatidosis in BALB/c mice with six groups, a group of females and another group of males was infected with PSC of Echinococcus, granulosus. Another two groups were gonadectomised and infected with PSC. and another two groups were healthy controls. They were all bled and sacrificed after sixteen weeks post-infection. The cysts in the abdominal cavity were count, and samples were taken from liver. A microscopic study was made of the tissue around the cyst to evaluate the chronic inflammatory response. In addition the seric levels of estradiol and testosterone by means of radioimmunoassay (RIA) were determined. The results were that the females presented a greater number of cysts in liver than the males, in addition the levels to estradiol almost rose to the double in males and females after 16 weeks post-infection, and the testosterone diminished. The granulomatous response around the cysts was greater in the females than in the males. The gonadectomization affected the susceptibility to the infection in females, diminishing in number of hepatic cysts found. One concluded that the females are more susceptible to the infection by metacestode of E. granulosrus, than the males. The female displayed one better granulomatous answer than the males. Nevertheless this was not sufficient to eliminate the parasite or to inhibit its growth. The levels of estradiol and testosterone undergo an imbalance, observing that estradiol increased in chronic stages of the infection whereas the testosterone diminishes, which would indicate to us that probably the parasite causes hormonal imbalance in chronic stages, to be able to remain by long periods in its host.
{"title":"Gender as a factor of susceptibility to infection in experimental hydatidosis.","authors":"Marisol Blancas Mosqueda, Rafael Herrera Esparza, Cristina Rodríguez Padilla, Jesús Patricio Tavizón García, Marisa Mercado Reyes, Valentin Badillo Almaraz, Francisco Echavarría, Adrián López Saucedo, Carmen Mondragón de la Peña","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>We developed an experimental model of hydatidosis in BALB/c mice with six groups, a group of females and another group of males was infected with PSC of Echinococcus, granulosus. Another two groups were gonadectomised and infected with PSC. and another two groups were healthy controls. They were all bled and sacrificed after sixteen weeks post-infection. The cysts in the abdominal cavity were count, and samples were taken from liver. A microscopic study was made of the tissue around the cyst to evaluate the chronic inflammatory response. In addition the seric levels of estradiol and testosterone by means of radioimmunoassay (RIA) were determined. The results were that the females presented a greater number of cysts in liver than the males, in addition the levels to estradiol almost rose to the double in males and females after 16 weeks post-infection, and the testosterone diminished. The granulomatous response around the cysts was greater in the females than in the males. The gonadectomization affected the susceptibility to the infection in females, diminishing in number of hepatic cysts found. One concluded that the females are more susceptible to the infection by metacestode of E. granulosrus, than the males. The female displayed one better granulomatous answer than the males. Nevertheless this was not sufficient to eliminate the parasite or to inhibit its growth. The levels of estradiol and testosterone undergo an imbalance, observing that estradiol increased in chronic stages of the infection whereas the testosterone diminishes, which would indicate to us that probably the parasite causes hormonal imbalance in chronic stages, to be able to remain by long periods in its host.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"49 1-2","pages":"31-7"},"PeriodicalIF":0.0,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27589387","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nora Molina, Daniela Polverino, Marta Minvielle, Juan Basualdo
Giardia lamblia (syn G. intestinalis, G. duodenalis) is the intestinal protozoan producing non-bacterial diarrhea most prevalent in the world. PCR genotype classification of Giardia in feces depends on the quality and quantity of purified DNA and the removal of a great number of inhibitors. The aim of this study was to adapt a PCR protocol to the amplification of the triosephosphate isomerase (tpi) gene of Giardia lamblia in formalin-fixed feces. The tpi gene of G. lamblia was amplified in 28 of the 34 analyzed samples (82.35%) and the B genotype was obtained in all cases. Two major modifications were implemented to improve the performance of PCR from formolated fecal matter. One of these improvements was the use of polyvinylpyrrolidone (PVP) and the other was the addition of bovine serum albumin (BSA). The PCR protocol used in this study showed an amplification percentage exceeding the values reported by other authors with high sensibility and specificity.
{"title":"PCR amplification of triosephosphate isomerase gene of Giardia lamblia in formalin-fixed feces.","authors":"Nora Molina, Daniela Polverino, Marta Minvielle, Juan Basualdo","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Giardia lamblia (syn G. intestinalis, G. duodenalis) is the intestinal protozoan producing non-bacterial diarrhea most prevalent in the world. PCR genotype classification of Giardia in feces depends on the quality and quantity of purified DNA and the removal of a great number of inhibitors. The aim of this study was to adapt a PCR protocol to the amplification of the triosephosphate isomerase (tpi) gene of Giardia lamblia in formalin-fixed feces. The tpi gene of G. lamblia was amplified in 28 of the 34 analyzed samples (82.35%) and the B genotype was obtained in all cases. Two major modifications were implemented to improve the performance of PCR from formolated fecal matter. One of these improvements was the use of polyvinylpyrrolidone (PVP) and the other was the addition of bovine serum albumin (BSA). The PCR protocol used in this study showed an amplification percentage exceeding the values reported by other authors with high sensibility and specificity.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"49 1-2","pages":"6-11"},"PeriodicalIF":0.0,"publicationDate":"2007-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27589470","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
All submerged cultures are under forces associated to fluid dinamics. In this review, the bases of hydrodynamic stress in agitated systems of submerged cultures will be presented, starting from the definitions of eddy of microscale, shear stress and shear rate. This work reports as well some of the most important proposals of cellular response of cells affected by shear injuries, and how other stress response mechanisms allow the cell to respond to the hydrodynamic effects. In addition, some of the most remarkable reports in each one of the cellular culture models will be presented that can be affected by the mechanical agitation, such as: bacteria, filamentous fungi, vegetal and animal cells.
{"title":"[Hydrodynamic stress: death and cellular damage in agitated cultures].","authors":"Mauricio A Trujillo-Roldán, Norma A Valdez-Cruz","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>All submerged cultures are under forces associated to fluid dinamics. In this review, the bases of hydrodynamic stress in agitated systems of submerged cultures will be presented, starting from the definitions of eddy of microscale, shear stress and shear rate. This work reports as well some of the most important proposals of cellular response of cells affected by shear injuries, and how other stress response mechanisms allow the cell to respond to the hydrodynamic effects. In addition, some of the most remarkable reports in each one of the cellular culture models will be presented that can be affected by the mechanical agitation, such as: bacteria, filamentous fungi, vegetal and animal cells.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"48 3-4","pages":"269-80"},"PeriodicalIF":0.0,"publicationDate":"2006-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27281492","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Rocio Ivette Lopez-Roa, Mary Fafutis-Morris, Matsuoka Masanori
A skin biopsy sample was obtained from a relapsed lepromatous leprosy patient from the central area of Mexico. Genes associated with resistance to anti-leprosy drugs were analyzed by DNA sequence assay. A single nucleotide substitution was found at codon 53 (ACC-->GCC) in the folP gene, which is known to confer dapsone resistance. No mutations in the rpoB and gyrA, which indicate resistance to rifampicin and fluoroquinoles, were detected. This is the first reported case of dapsone resistant leprosy in Mexico in which the cause of the resistance is shown at genomic level. Evaluation of drug resistance by identifying known mutations in these genes by PCR is simple and reliable. Testing for resistance to anti-leprosy drugs should be performed in relapses or intractable cases for a better outcome.
{"title":"A drug-resistant leprosy case detected by DNA sequence analysis from a relapsed Mexican leprosy patient.","authors":"Rocio Ivette Lopez-Roa, Mary Fafutis-Morris, Matsuoka Masanori","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>A skin biopsy sample was obtained from a relapsed lepromatous leprosy patient from the central area of Mexico. Genes associated with resistance to anti-leprosy drugs were analyzed by DNA sequence assay. A single nucleotide substitution was found at codon 53 (ACC-->GCC) in the folP gene, which is known to confer dapsone resistance. No mutations in the rpoB and gyrA, which indicate resistance to rifampicin and fluoroquinoles, were detected. This is the first reported case of dapsone resistant leprosy in Mexico in which the cause of the resistance is shown at genomic level. Evaluation of drug resistance by identifying known mutations in these genes by PCR is simple and reliable. Testing for resistance to anti-leprosy drugs should be performed in relapses or intractable cases for a better outcome.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"48 3-4","pages":"256-9"},"PeriodicalIF":0.0,"publicationDate":"2006-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27281083","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marco Adán Juárez-Verdayes, Miguel Angel Reyes-López, Mario Eugenio Cancino-Díaz, Susana Muñoz-Salas, Sandra Rodríguez-Martínez, Francisco Javier Zavala-Díaz de la Serna, César Hugo Hernández-Rodríguez, Juan Carlos Cancino-Díaz
The infection frequency associated to bacterial conjunctivitis, corneal ulcers (CU), and endophthalmitis was studied along a five years period. The isolation and identification of microorganisms were performed by culture-based methods and biochemical test respectively. Also, a nested PCR to detect gram-negative and gram-positive bacteria in the clinical samples was assayed. Nested PCR was a more efficient method than culture to detect bacteria in the samples. The most frequently isolated species was Staphylococcus epidermidis, a bacterium commonly considered as a human saprophyte. The S. epidermidis strains from conjunctivitis, CU, and endophthalmitis exhibited 46, 33.9, and 34.1% of oxacilin-resistance respectively. A total of 28% of intermediate-vancomycin resistance (MIC = 8-16 microg/ml) was observed among S. epidermidis strain collection. The UPGMA cluster analysis of the multiresistance profile data of intermediate vancomycin-resistant S. epidermidis strains showed a high phenotypic diversity and no relationship between each group and their clinical origin. The biofilm formation capacity was broadly distributed (66%), particularly among intermediate-vancomycin strains (> 75%). In brief, S. epidermidis displayed a high diversity of antibiotic resistance profiles and biofilm formation capacity. These phenotypic traits could explain the high isolation frequency of S. epidermidis from ocular infections and oblige to review the saprophytic status of these bacteria.
{"title":"Isolation, vancomycin resistance and biofilm production of Staphylococcus epidermidis from patients with conjunctivitis, corneal ulcers, and endophthalmitis.","authors":"Marco Adán Juárez-Verdayes, Miguel Angel Reyes-López, Mario Eugenio Cancino-Díaz, Susana Muñoz-Salas, Sandra Rodríguez-Martínez, Francisco Javier Zavala-Díaz de la Serna, César Hugo Hernández-Rodríguez, Juan Carlos Cancino-Díaz","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The infection frequency associated to bacterial conjunctivitis, corneal ulcers (CU), and endophthalmitis was studied along a five years period. The isolation and identification of microorganisms were performed by culture-based methods and biochemical test respectively. Also, a nested PCR to detect gram-negative and gram-positive bacteria in the clinical samples was assayed. Nested PCR was a more efficient method than culture to detect bacteria in the samples. The most frequently isolated species was Staphylococcus epidermidis, a bacterium commonly considered as a human saprophyte. The S. epidermidis strains from conjunctivitis, CU, and endophthalmitis exhibited 46, 33.9, and 34.1% of oxacilin-resistance respectively. A total of 28% of intermediate-vancomycin resistance (MIC = 8-16 microg/ml) was observed among S. epidermidis strain collection. The UPGMA cluster analysis of the multiresistance profile data of intermediate vancomycin-resistant S. epidermidis strains showed a high phenotypic diversity and no relationship between each group and their clinical origin. The biofilm formation capacity was broadly distributed (66%), particularly among intermediate-vancomycin strains (> 75%). In brief, S. epidermidis displayed a high diversity of antibiotic resistance profiles and biofilm formation capacity. These phenotypic traits could explain the high isolation frequency of S. epidermidis from ocular infections and oblige to review the saprophytic status of these bacteria.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"48 3-4","pages":"238-46"},"PeriodicalIF":0.0,"publicationDate":"2006-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27281123","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
C Alvarado, B E García Almendárez, S E Martin, C Regalado
This work was conducted to identify indigenous LAB capable of antimicrobial activity, present in traditional Mexican-foods with potential as natural preservatives. A total of 27 artisan unlabeled Mexican products were evaluated, from which 94 LAB strains were isolated, and only 25 strains showed antimicrobial activity against at least one pathogen indicator microorganism. Most of the inhibitory activity showed by the isolated LAB strains was attributed to pH reduction by organic acids. Lactobacillus and Lactococcus strains were good acid producers, depending on the substrate, and may enhance the safety of food products. Cell free cultures of Leuconostoc mesenteroides CH210, and PT8 (from chorizo and pulque, respectively) reduced the number of viable cells of enteropathogenic E. coli in broth system. Lb. plantarum CC10 (from "madre" of vinegar) showed significant inhibitory effect against S. aureus 8943. E. faecium QPII (from panela cheese) produced a bacteriocin with wide anti-L. monocytogenes activity. Selected LAB from traditional Mexican foods showed good potential as bio-preservatives.
{"title":"Food-associated lactic acid bacteria with antimicrobial potential from traditional Mexican foods.","authors":"C Alvarado, B E García Almendárez, S E Martin, C Regalado","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>This work was conducted to identify indigenous LAB capable of antimicrobial activity, present in traditional Mexican-foods with potential as natural preservatives. A total of 27 artisan unlabeled Mexican products were evaluated, from which 94 LAB strains were isolated, and only 25 strains showed antimicrobial activity against at least one pathogen indicator microorganism. Most of the inhibitory activity showed by the isolated LAB strains was attributed to pH reduction by organic acids. Lactobacillus and Lactococcus strains were good acid producers, depending on the substrate, and may enhance the safety of food products. Cell free cultures of Leuconostoc mesenteroides CH210, and PT8 (from chorizo and pulque, respectively) reduced the number of viable cells of enteropathogenic E. coli in broth system. Lb. plantarum CC10 (from \"madre\" of vinegar) showed significant inhibitory effect against S. aureus 8943. E. faecium QPII (from panela cheese) produced a bacteriocin with wide anti-L. monocytogenes activity. Selected LAB from traditional Mexican foods showed good potential as bio-preservatives.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"48 3-4","pages":"260-8"},"PeriodicalIF":0.0,"publicationDate":"2006-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27281079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
D Calvo, L N Cariddi, M Grosso, M S Demo, A M Maldonado
Achyrocline satureioides (LAM.) DC (Compositae) is a sub-bush original from America and distributed in Europe and Africa. It is mainly used in infusions, as digestive, sedative among others and has antimicrobial and antiviral properties. A research was made into the anti-microbial activity of the A. satureioides decoction on the Staphylococcus spp strains. They were isolated from 18 patients with acne lesions and from 7 patients infected with Staphylococcus spp. (5 strains were taken from catheters and 2 from wounds). The strains were classified through biochemical tests and then were seeded in triptein-soy agar with or without decoction to observe the antibacterial activity. On the other hand, cultures of lymphocytes were made from those patients who displayed infections caused by Staphylococcus spp. and from 12 control non-infected individuals. The lymphocytes were stimulated with decoction or PHA-M. Among the expanded, CD8+ T cells, with anti-human CD8 monoclonal antibody were the outstanding ones by indirect IF. The A. satureiodes decoction inhibited 95% of the isolated Staphylococcus spp. strains and stimulated the lymphocyte expansion, of which 40% were CD8+ T cells. The A. satureiodes decoction showed anti-microbial activity and resulted to be an immunostimulating agent on CD8+ T cells, with lesser mitogenic effects than PHA-M.
{"title":"Achyrocline satureioides (LAM.) DC (Marcela): antimicrobial activity on Staphylococcus spp. and immunomodulating effects on human lymphocytes.","authors":"D Calvo, L N Cariddi, M Grosso, M S Demo, A M Maldonado","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Achyrocline satureioides (LAM.) DC (Compositae) is a sub-bush original from America and distributed in Europe and Africa. It is mainly used in infusions, as digestive, sedative among others and has antimicrobial and antiviral properties. A research was made into the anti-microbial activity of the A. satureioides decoction on the Staphylococcus spp strains. They were isolated from 18 patients with acne lesions and from 7 patients infected with Staphylococcus spp. (5 strains were taken from catheters and 2 from wounds). The strains were classified through biochemical tests and then were seeded in triptein-soy agar with or without decoction to observe the antibacterial activity. On the other hand, cultures of lymphocytes were made from those patients who displayed infections caused by Staphylococcus spp. and from 12 control non-infected individuals. The lymphocytes were stimulated with decoction or PHA-M. Among the expanded, CD8+ T cells, with anti-human CD8 monoclonal antibody were the outstanding ones by indirect IF. The A. satureiodes decoction inhibited 95% of the isolated Staphylococcus spp. strains and stimulated the lymphocyte expansion, of which 40% were CD8+ T cells. The A. satureiodes decoction showed anti-microbial activity and resulted to be an immunostimulating agent on CD8+ T cells, with lesser mitogenic effects than PHA-M.</p>","PeriodicalId":21464,"journal":{"name":"Revista latinoamericana de microbiologia","volume":"48 3-4","pages":"247-55"},"PeriodicalIF":0.0,"publicationDate":"2006-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"27281125","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}