2002
DOI: 10.1016/s0923-2508(01)01284-0
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Differentiation of leptospires of the serogroup Pomona by monoclonal antibodies, pulsed-field gel electrophoresis and arbitrarily primed polymerase chain reaction

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Cited by 19 publications
(15 citation statements)
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“…However, our use of PFGE and gyrB sequence analysis as alternative methods for typing isolates have been done in other studies of leptospirosis. 6,7,22,26,28,29,38,53 The results of our study provide useful information on the epidemiology of leptospirosis in the Philippines, which until now was not well studied. However, studies with larger sample sizes on leptospirosis among rats, humans, and other animals in other areas of the Philippines would be beneficial in determining the transmission cycle of leptospirosis and the status of this zoonosis.…”
Section: Discussionmentioning
confidence: 90%
“…However, our use of PFGE and gyrB sequence analysis as alternative methods for typing isolates have been done in other studies of leptospirosis. 6,7,22,26,28,29,38,53 The results of our study provide useful information on the epidemiology of leptospirosis in the Philippines, which until now was not well studied. However, studies with larger sample sizes on leptospirosis among rats, humans, and other animals in other areas of the Philippines would be beneficial in determining the transmission cycle of leptospirosis and the status of this zoonosis.…”
Section: Discussionmentioning
confidence: 90%
“…Animal populations of the same species can exhibit either chronic or acute infections with serovar Pomona. Restriction fragment length polymorphism (RFLP) analysis of L. interrogans serovar Pomona isolates has revealed the presence of two major subtypes (5,22) that can be further differentiated by HpaII digestion (2) or IS1500 hybridization (24) patterns. Specific clonal populations, rather than all members of serovar Pomona, may form stable associations with selected maintenance host species (2).…”
mentioning
confidence: 99%
“…A maioria dessas técnicas apresenta limitações de ordem prática resultantes da complexidade, lentidão dos procedimentos para detectar e caracterizar o agente infeccioso ou ainda infraestrutura laboratorial necessária, além das limitações relativas à sensibilidade e especificidade, que são fatores complicadores para a realização de diagnóstico de baixo custo, prático e preciso (CICERONI et al, 2002;MANTEROLA et al, 2003). Assim, torna-se necessário a busca por métodos que apresentem mais especificidade, sensibilidade e rapidez no diagnóstico de bactérias no sêmen de touros a campo e de central de inseminação.…”
Section: Resultado E Discussãounclassified