Abstract. Antibiotic-resistant bacteria are becoming more common around the world
each day. Terrestrial actinomycetes are the major sources of known antibiotics. However,
the number of new antibiotics found in terrestrial soils has fallen dramatically over the
last 20 years. Marine environments and mangroves are seen as untapped environments
which have high potential for new drug discovery. Actinomycetes strain QN63 was
isolated from sediment collected in a mangrove environment in Yen Hung District,
Quang Ninh Province, and it has been found to inhibit antibiotic-resistant
Staphylococcus aureus. Morphological and molecular identification shows that QN63 is
a strain of Streptomyces shenzhenensis. The identification of this strain and the published
results of its antibiotic properties suggest that S. shenzhenensis QN63 might be effective
in treating infections caused by antibiotic resistant Staphylococcus aureus.
7 trang |
Chia sẻ: thanhle95 | Lượt xem: 29 | Lượt tải: 0
Bạn đang xem nội dung tài liệu Identification of Streptomyces sp. QN63 against antibiotic-resistant Staphylococcus aureus, để tải tài liệu về máy bạn click vào nút DOWNLOAD ở trên
JOURNAL OF SCIENCE OF HNUE DOI: 10.18173/2354-1059.2015-00086
Chemical and Biological Sci. 2015, Vol. 60, No. 9, pp. 112-118
This paper is available online at
Received December 8, 2015. Accepted December 28, 2015.
Contact Duong Minh Lam, e-mail address: duong.minhlam@gmail.com
112
IDENTIFICATION OF Streptomyces sp. QN63
AGAINST ANTIBIOTIC-RESISTANT Staphylococcus aureus
Duong Minh Lam, Truong Thi Chien a d Tran Thi Thuy
Faculty of Biology, Hanoi National University of Education
Abstract. Antibiotic-resistant bacteria are becoming more common around the world
each day. Terrestrial actinomycetes are the major sources of known antibi tics. However,
the number of new antibiotics found in terrestrial soils has fallen dramatically over the
last 20 years. Marine environments and mangroves are seen as untapped environments
which have high potential for new drug discovery. Actinomycetes strain QN63 was
isolated from sediment collected in a mangrove environment in Yen Hung District,
Quang Ninh Province, and it has been found to inhibit antibiotic-resis ant
Staphylococcus aureus. Morphological and molecular identification shows that QN63 is
a strain of Streptomyces shenzhenensis. The identification of this strain and the published
results of its antibiotic properties suggest that S. shenz enensis QN63 might be effective
in treating infections caused by antibiotic resistant Staphylococcus aureus.
Keywords: Streptomyces sp. QN63, Streptomyces shenzhenensis, Staphylococcus aureus,
antibiotic resistant, mangroves.
1. Introduction
Methicillin Resistant Staphylococcus aureus-MRSA has become universal problem as it
resists almost every antibiotic tha has been used to kill it, including vancomycin. Twenty-f ve
years ago, in 1991, more than a half of the S. aureus strains isolated in the United States of
America (USA) were found to be capable of resisting penicillin, methicillin, tetracycline and
erythromycin [1].
Vancomycin was the only antibiotic that was effective against S. aureus at that time.
However, in 1996, a vancomycin-resistant S. aureus strain at the concentration of 4 - 8 µg/mL
was found in Japan, and then in France, England and the USA [1]. In 2002, Silvestri et al. [2]
found a vancomycin-resistant S. aureus strain at much higher concentration (16 µg/mL).
However, treatment of severe MRSA infections ontinues to be vancomycin but now at
trough levels of ≥ 15 mg/L [3].
Some scientists had suggested that the drug resistant bacteria w e all one strain of
MRSA [2]. S. aureus had infected almost 1/3 of world‟s population, and it has become a
threat to public health. Traditional drugs could not combat this problem of antibiotic
resistance [4]. In an attempt to control the spread of MRSA, there has been an increase in
Identification of Streptomyces sp. QN63 against antibiotic-resistant staphylococcus aureus
113
patient screening, decontamination, surveillance and contact isolation; n alert system has
been created; hand washing in hospitals has become mandatory and the search for new
antibiotics continues [5]. With integrated prevention methods, the number of healthcare
associated MRSA S. aureus infections (HA-MRSA) decreased at the university hospital in
Geneva, Switzerland [5, 6].
Vietnam is a country in which a high percentage of bacteria are antibiotic-resistant.
Of the many patients in Hospital 175 who acquired an S. aureus infection, 55 strains were
identified and 50 - 70% of those strains resisted treatment with ampicillin, co-trimoxazol,
erythromycin, licomycin a d methicillin. The rate of resistance to axacilin increased from
9.6% in 1989 to 20.7% in 1994 [7]. And indeed most of the antibiotics in use at that time to
treat S. aureus infections had become ineffective. Looking for new and effective antibiotics to
treat drug resistant S. aureus has been and is a pressing need.
During our research on the screening that has been done in the search for new and valuable
antibiotics from mangrove actinomycetes, strain QN63 that was isolated from soil samples in
Yen Hung District, Quang NinhProvince was one which showed high activity against S. aureus
which were resistant to penicillin. Antibiotics produced by the QN63 strain were purified and
the chemical structure was determined to be cyclic peptide. It was a thermostable antibiotic,
remaining active 30 minutes after incubation at 80 oC [8]. Research that has been done showed
that antibiotics produced by the QN63 strain had high potential for application in treating drug
resistant S. aureus. In order to get closer to the goal identification to species level of the studied
strain is necessary and additional clinical studies on animals are also required. This paper
presents a more detailed identification of the QN63 strain based on morphological and
molecular characteristics.
2. Content
2.1. Materials and methods
2.1.1. Materials
- Subject: The QN63 strain was isolated from soil samples collected from Yen Hung
mangrove sediment, Quang Ninh Province.
- Test microorganism: Staphylococcus aureus 30sd from the collection of the Department
of Microbiology and Biotechnology, Hanoi National University of Education, Vietnam.
- Media: Czapek-glucose (glucose 30.0 g; KCl 0.5 g; NaNO3 3.0 g; FeSO4 0.01 g;
K2HPO4 1.0 g; MgSO4.7H2O 0.5 g; agar 20 g; sea water 1000 mL); Gause I (starch 20 g,
FeSO4 0.01 g, K2HPO4 0.5 g, agar 20 g, MgSO4 0.5 g, KNO3 0.5 g, sea water 1000 mL, pH 7.2 - 7.4);
Gause II (glucose 10 g, meat extract 3 g, pepton 5g, agar 20 g, sea water 1000 mL, pH 7.0 - 7.2);
MPA (meat extract 5 g, peptone 5 g, NaCl 5 g, agar 20 g, sea water 1000 ml, pH 7.0-7.2). A4
(glucose 10 g, soybean powder 10 g, CaCO3 1 g, agar 20 g, sea water 1000 mL, pH 7.0); A4H
(glucose 15 g, soybean powder 5 g, CaCO3 1 g, agar 20 g, sea water 1000 mL, pH 7.0);
Soybean powder medium (soybean 15 g, glycerine 2.5 g, glucose 15 g, peptone 5 g, CaCO3 1 g,
agar 20 g, sea water 1000 mL, pH 7.0).
2.1.2. Methods
* Morphological description
The strain QN63 was grown on different media for 10 days and then described
morphologies of colonies, aerial and substrate hyphae, conidiophores using light microscope.
Duong Minh Lam, Truong Thi Chien a d Tran Thi Thuy
114
* Electron microscopic descriptions
Electron microscopic graphs were taken to analyze the characteristics of the
conidiophores and spores. This was done at the National Institute of Hygiene and
Epidemiology, Hanoi, Vietnam.
* DNA isolation, PCR and phylogenetic analysis
DNA isolation was done using the method described in Sambrookvà Russell (2001) [9].
PCR and sequencing
Partial sequences of the DNA coding for 16S rRNA was amplified using the universal
primer pair (forward primer 314F: 5‟-CCTACGGGAGGCAGCAG-3‟ and reverse primer 907R:
5‟-CCGTCAATTCCTTTGAGTTT-3‟) with PCR master mix produced by the Bioneer Company,
Korea. The PCR products were purified using a QiaGen purification kit before sending out for
sequencing by the Gentis Company, Vietnam. The consensus sequence was combined from
both forward and reverse sequences.
Phylogenetic analysis
The sequence of the QN63 strain was used to search for similar sequences available in
the Genbank through the nucleotide blast program (nBlast-NCBI) [10]. All sequences used in
the analysis were anneled using ClustalX software [11] and then optimized in the BioEdit
program [12]. The Neighbor-Joining analysis was applied for phylogenetic analysis of the
studied sequence with 31 other selected Str ptomyces sequences in the Genbank. Two
sequences, Bacillus thuringiensis (EF206345) and B. gibsonii (AY737309), were used as the
outgroup. A Bootstrap analysis was done using 1000 replicates.
2.2. Results
2.2.1. Morphological descriptions
The QN63 strain was cultured in 7 different media, each containing a different carbon
source, to assess microscopic morphological characteristics, pigments secreted into the medium
(Table 1), and shapes and sizes of conidiophores and spores. Figure 1 shows the conidiop res
of the QN63 strain in the seven different media.
Figure 1. Conidiophores and hyphae of the QN63 strain on different media
a) Czapek-glucose; b) Gause I; c) ISP 4
Based on morphological characteristics of colonies and microscopic morphological
characteristics of conidiophores, the QN63 strain was found to possess typical characteristics of
the Streptomyces genus, identifying the strain as of the species Streptomyces. However, more
details are required to make a more precise identification.
Identification of Streptomyces sp. QN63 against antibiotic-resistant staphylococcus aureus
115
Table 1. Morphological characteristics of the QN63 strain on 7 growth media
Criteria
Media
Growth
rate
Aerial
hyphae
Substrate
hyphae
Pigment Conidiospores
Gause I: Conidiophores
visible at 5 days of
growth
Well
(+++)
Pinkish
Grey Grey -
- Well-developed spores
- Spiral conidiophores
ISP4: Conidiophores
visible at 5 days of
growth
Very
well
(++++)
White Grey -
- Well-developed spores
- Straight-Spiral
conidiophores
Gause II Weak (+) White Grey
Present,
Dark
brown
- Poorly-developed
spores
- Spiral conidiophores
Czapek-dox Weak (+) White Grey -
- Well-developed spores
- Spiral conidiophores
Czapek-glucose Average (++) White Grey -
- Ppoorly-developed
spores
- Spiral conidiophores
Czapek-starch:
conidiophores visible at
day 10th of growth
Well
(+++)
Whitish-
grey Grey -
- Well-developed spores
- Straight-Spiral
conidiophores
MPA with sea water:
spores not formed after
15 days of growth
Week
(+) Grey Grey
Present,
dark
brown
- Not yet formed
2.2.2. Morphologies under the electron microscope
Figure 2. Conidiophores and spores of the strain Streptomyces sp. QN63
a) on Gause I; b) on Czapek-starch
The light and electron microscopy were used to distinguish characteristics (Figure 2) of the
conidiophores and spore chain of the Streptomyces sp. QN63 on different media and they
showed the typical spiral spore chain of Streptomyces. The conidiophores were small (0.4 -
0.6 x 1.2 - 1.4 µm) bearing a chain of 18 - 40 spores. The spores are cylindrical, wrinkled
without appendages (hair, spines...) and relatively sm ll, 0.8 - 0.9 µm wide x 0.8 - 1.2 µm long
(Figure 2). The characteristics revealed by electron microscopy confirmed that QN63 is a
Duong Minh Lam, Truong Thi Chien a d Tran Thi Thuy
116
strain of Streptomyces. Streptomyces is a genera that is one of the most famous genera for
antibiotic producing ability and it is one of the most abundant microorganisms in the world.
However, the features revealed by culture test and electron features are not sufficient to
identify which species of Streptomyces the strain is. DNA analysis provides additional
information for a better identification.
2.2.3. Phylogenetic analysis
Figure 3. Neighbor-Joining phylogenetic tree based on the partial 16S rRNA gene
sequences of the Streptomyces sp. QN63 strain and 31 phylogenetically
closely related representative species of the genus Streptomyces.
Numbers at branching points indicate bootstrap percentages
(based on 1,000 replications)
Identification of Streptomyces sp. QN63 against antibiotic-resistant staphylococcus aureus
117
A partial DNA sequence encoding 16S rRNA fragment, which consists of 531 nucleotides,
was used for comparison purposes to search for highly similar sequences in the GenBank. The
sequence KM203728 of Streptomyces shenzhenensis was found to be 99.8% similar (531/532
nucleotides). A set of 34 sequences including 32 sequences of the genus Streptomyces and the
two sequences of Bacillus in which Bacillus sequences were used as out group. Neighbor-
Joining analysis showed that the Streptomyces sp. QN63 strain was closest to Streptomyces
shenzhenensis KM203728 with the bootstrap value of 77.9%. With this additional information,
it was concluded that QN63 is of the genus Streptomyces and species shenzhenensis, denoted as
S. shenzhenensis QN63.
Streptomyces shenzhenensis was first presented as a new species in a publication in 2011. It
was isolated from mangrove sediment in Shenzhen District, Guangdong Province, China [13].
With the finding of S. shenzhenensis in the Yen Hung mangroves, it has been suggested that
mangrove actinomycetes could be dispersed in coastal water flows. The coastal mangroves of
Yen Hung (Quang Ninh Province, Vietnam) and Shenzhen (Guangdong Province, China) are
900 km from each other.
3. Conclusion
The actinomycete strain, QN63, which inhibited antibiotic-resistan Staphylococcus
aureus, was isolated from mangrove sediment in Yen Hung District, Quang Ninh Province. It
was identified asStreptomyces shenzhenensis based on light and electron microscopy revealed
features along with molecular characteristics and the strain in question is now referred as S.
shenzhenensis QN63. Identifying the strain to the species level is basic information needed for
further practical and clinical study of S. shenzhenensis QN63.
REFERENCES
[1] Hiramatsu K, Hanaki H, Ino T, Yabuta K, Oguri T, Tenover FC., 1997. Methicillin-
resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility.
Journal of Antimicrobial Chemotherapy Vol. 40, pp. 135-136.
[2] Silvestri L, Milanese M, Oblach L, Fontana F, Gregori D, Guerra R, van Saene H.,
2002. Enteral vancomycin to control methicillin-resistant Staphylococcus aureus
outbreak in mechanically ventilated patients. American Journal of Infection Control 30:
pp. 391-399.
[3] Steinmetz T, Eliakim-Raz N, Goldberg E, Leibovici L, Yahav D, 2015. Association of
vancomycin serum concentrations with efficacy in patients with MRSA infections: a
systematic review and meta-analysis. Clinical Microbiology and Infection Vol. 21,
No.7, pp. 665-67.
[4] Richardson AR, Libby SJ, Fang FC, 2015. A Nitric Oxide–Inducible Lactate
Dehydrogenase Enables Staphylococcus aureus to Resist Innate Immunity. Science 319:
pp. 1672-1676.
[5] Fankhauser C, Schrenzel J, Francois P, Pittet D, Harbarth S. 2015. Secular trends of
methicillin-resistant Staphylococcus aureus (MRSA) at Geneva University Hospitals
(HUG) over a 14-year period. Antimicrobial Resistance and Infection Control 2015,
4(Suppl 1):O9
Duong Minh Lam, Truong Thi Chien a d Tran Thi Thuy
118
[6] Olearo F, Albrich W, Harbarth S, Kronenberg A. 2015. Ten years of MRSA surveillance
in Switzerland: similarities and differences with Europe. Antimicrobial Resistance and
Infection Control 2015, 4(Suppl 1):O8
[7] Vu Bao Chau, 2000. Antibiotic resistant level of some bacteria isolated from infected
surgeries at hospital 175. 9-11-
2000.htm.
[8] Duong Minh Lam, Dang Ngoc Quang, Nguyen Thi Ha. 2013. Isolation, purification
and characterization of drug resistant Staphylococcus aureus antibiotics by
Streptomyces sp. QN63. Journal of Sciences and Technology V l. 51, No. 5: pp. 555-563.
[9] Sambrook J, Russell D., 2001. Molecular Cloning: A Laboratory Manual, 3rd ed. Cold
Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
[10]
&LINK_LOC=blasthome.
[11] Thompson JD, Gibson TJ, Plewniak F, Higgins DG, 1997. The Clustal X windows
interface: flexible strategies for multiple sequence alignment aided by quality analysis
tools. Nuc. Acid. Res., 24: pp.4876-4882.
[12] Hall TA., 1999. BioEdit: a user-friendly biological sequence alignment editor and
analysis program for Windows 95/98/NT. Nuc. Acid. Symp. Ser., Vol. 41, pp. 95-98.
[13] Lin HP, Xie Q, Li L, Xie XQ, Sun M, Hong K, 2011. Streptomyces shenzhenensis sp.
nov., a novel actinomycete isolated from mangrove sediment. Antonie Van
Leeuwenhoek Vol. 100, pp. 631-637.