Visualizing aquatic bacteria by light and transmission electron microscopy

被引:21
作者
Silva, Thiago P. [1 ]
Noyma, Natalia P. [2 ]
Duque, Thabata L. A. [1 ]
Gamalier, Juliana P. [1 ]
Vidal, Luciana O. [2 ]
Lobao, Lucia M. [2 ]
Chiarini-Garcia, Helio [3 ]
Roland, Fabio [2 ]
Melo, Rossana C. N. [1 ]
机构
[1] Univ Fed Juiz de Fora, Lab Cellular Biol, Dept Biol, BR-36036900 Juiz de Fora, MG, Brazil
[2] Univ Fed Juiz de Fora, Aquat Ecol Lab, Dept Biol, BR-36036900 Juiz de Fora, MG, Brazil
[3] Univ Fed Minas Gerais, Lab Struct Biol & Reprod, Dept Morphol, BR-31270901 Belo Horizonte, MG, Brazil
来源
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY | 2014年 / 105卷 / 01期
关键词
Aquatic bacteria; Ultrastructure; Fluorescence microscopy; Aquatic ecosystems; Cell viability; Electron microscopy; GRAM-NEGATIVE BACTERIA; MEMBRANE-VESICLES; DIRECT ENUMERATION; VIABILITY; ENVELOPE; ULTRASTRUCTURE; ORGANIZATION; PRINCIPLES; ABUNDANCE; MESOSOMES;
D O I
10.1007/s10482-013-0047-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The understanding of the functional role of aquatic bacteria in microbial food webs is largely dependent on methods applied to the direct visualization and enumeration of these organisms. While the ultrastructure of aquatic bacteria is still poorly known, routine observation of aquatic bacteria by light microscopy requires staining with fluorochromes, followed by filtration and direct counting on filter surfaces. Here, we used a new strategy to visualize and enumerate aquatic bacteria by light microscopy. By spinning water samples from varied tropical ecosystems in a cytocentrifuge, we found that bacteria firmly adhere to regular slides, can be stained by fluorochoromes with no background formation and fast enumerated. Significant correlations were found between the cytocentrifugation and filter-based methods. Moreover, preparations through cytocentrifugation were more adequate for bacterial viability evaluation than filter-based preparations. Transmission electron microscopic analyses revealed a morphological diversity of bacteria with different internal and external structures, such as large variation in the cell envelope and capsule thickness, and presence or not of thylakoid membranes. Our results demonstrate that aquatic bacteria represent an ultrastructurally diverse population and open avenues for easy handling/quantification and better visualization of bacteria by light microscopy without the need of filter membranes.
引用
收藏
页码:1 / 14
页数:14
相关论文
共 50 条
[41]   Transmission Electron Microscopy as Key Technique for the Characterization of Telocytes [J].
Cantarero, Irene ;
Jose Luesma, Maria ;
Miguel Alvarez-Dotu, Jose ;
Munoz, Eduardo ;
Junquera, Concepcion .
CURRENT STEM CELL RESEARCH & THERAPY, 2016, 11 (05) :410-414
[42]   Intracellular papillae of Actinocephalus (Eriocaulaceae-Poales) roots and their interaction with fungi:: A light and transmission electron microscopy study [J].
Oriani, Aline ;
Scatena, Vera L. .
MICRON, 2007, 38 (06) :611-617
[43]   The sexual dimorphic inguinal glands of the frog species Ololygon centralis (Anura: Hylidae) at light and transmission electron microscopy [J].
Brito, Pedro ;
Targueta, Cintia P. ;
Arruda, Walquiria ;
Santos, Fernanda ;
Bastos, Rogerio .
ZOOLOGIA, 2019, 36
[44]   Efficient fluorescence recovery using antifade reagents in correlative light and electron microscopy [J].
Toyooka, Kiminori ;
Shinozaki-Narikawa, Naeko .
MICROSCOPY, 2019, 68 (05) :417-421
[45]   Same serial section correlative light and energy-filtered transmission electron microscopy [J].
Ren, Y ;
Kruhlak, MJ ;
Bazett-Jones, DP .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2003, 51 (05) :605-612
[46]   Balamuthia mandrillaris: Further morphological observations of trophozoites by light, scanning and transmission electron microscopy [J].
Gonzalez-Robles, Arturo ;
Lares-Villa, Fernando ;
Fernando Lares-Jimenez, Luis ;
Omana-Molina, Maritza ;
Salazar-Villatoro, Lizbeth ;
Martinez-Palomo, Adolfo .
EXPERIMENTAL PARASITOLOGY, 2015, 157 :150-155
[47]   Light microscopy and electron microscopy of Nephroselmis spinosa sp Nov (Prasinophyceae, Chlorophyta) [J].
Suda, S .
JOURNAL OF PHYCOLOGY, 2003, 39 (03) :590-599
[48]   Structural Analysis of Cerebral Organoids Using Confocal Microscopy and Transmission/Scanning Electron Microscopy [J].
Noh, Seulgi ;
Park, Yurim ;
Kim, Beomsue ;
Mun, Ji Young .
MICROSCOPY AND MICROANALYSIS, 2025, 31 (01)
[49]   CLAFEM: correlative light atomic force electron microscopy [J].
Janel, Sebastien ;
Werkmeister, Elisabeth ;
Bongiovanni, Antonino ;
Lafont, Frank ;
Barois, Nicolas .
CORRELATIVE LIGHT AND ELECTRON MICROSCOPY III, 2017, 140 :165-185
[50]   A new entomopoxvirus from a cockroach: Light and electron microscopy [J].
Radek, R ;
Fabel, P .
JOURNAL OF INVERTEBRATE PATHOLOGY, 2000, 75 (01) :19-27