Skip to main content
Download PDF

MLVA and MLST typing of Brucella from Qinghai, China

Infectious Diseases of Poverty volume 5, Article number: 26 (2016) Cite this article

Abstract

Background

The Qinghai-Tibet Plateau (QTP) of China is an extensive pastoral and semi-pastoral area, and because of poverty and bad hygiene conditions, Brucella is highly prevalent in this region. In order to adequately prevent this disease in the QTP region it is important to determine the identity of Brucella species that caused the infection.

Methods

A total of 65 Brucella isolates were obtained from human, livestock and wild animals in Qinghai, a Chinese province in east of the QTP. Two molecular typing methods, MLVA (multi-locus variable-number tandem-repeat analysis) and MLST (multi locus sequence typing) were used to identify the species and genotypes of these isolates.

Findings

Both MLVA and MLST typing methods classified the 65 isolates into three species, B. melitensis, B. abortus and B. suis, which included 60, 4 and 1 isolates respectively. The MLVA method uniquely detected 34 (Bm01 ~ Bm34), 3 (Ba01 ~ Ba03), and 1 (Bs01) MLVA-16 genotypes for B. melitensis, B. abortus and B. suis, respectively. However, none of these genotypes exactly matched any of the genotypes in the Brucella2012 MLVA database. The MLST method identified five known ST types: ST7 and ST8 (B. melitensis), ST2 and ST5 (B. abortus), and ST14 (B. suis). We also detected a strain with a mutant type (3-2-3-2-?-5-3-8-2) of ST8 (3-2-3-2-1-5-3-8-2). Extensive genotype-sharing events could be observed among isolates from different host species.

Conclusions

There were at least three Brucella (B. melitensis, B. abortus and B. suis) species in Qinghai, of which B. melitensis was the predominant species in the area examined. The Brucella population in Qinghai was very different from other regions of the world, possibly owing to the unique geographical characteristics such as extremely high altitude in QTP. There were extensive genotype-sharing events between isolates obtained from humans and other animals. Yaks, sheep and blue sheep were important zoonotic reservoirs of brucellosis causing species found in humans.

Multilingual abstracts

Please see Additional file 1 for translations of the abstract into the six official working languages of the United Nations.

Introduction

Brucellosis is one of the most widespread and severe zoonotic diseases across the world. This disease affects mammals and is transmitted to humans by animals through direct contact with contaminated animal fluids or indirectly through consumption of unpasteurized milk products [1]. Brucellosis in domestic mammals and humans is the cause of huge economic burden and medical challenges globally, especially in poor regions [2–5]. The causal agent of brucellosis, Brucella genus, currently contains 10 species: B. abortus, B. suis, B. melitensis, B. ovis, B. canis, B. neotomae, B. ceti, B. pinnipedialis, B. microti, and B. inopinata. Some species are further subdivided into biovars, i.e., B. melitensis bv.1 to 3, B. abortus bv. 1 to 6 and 9, and B. suis bv. 1 to 5 [6]. Most species with a preferential host and three other species (B. abortus, B. melitensis, and B. suis) remain the principal causes of zoonotic potential [1].

Since different species or biovars within a species of Brucella have different epidemiological significances, in order to effectively prevent this disease, it is important to identify the species or strain of Brucella that causes infection. Most previous molecular subtyping tools and “classical biotyping” methods lack sufficient discriminatory power for epidemiological investigations. Recently, two molecular typing methods called MLVA (multi-locus variable-number tandem-repeat analysis) and MLST (multi locus sequence typing) have emerged as useful tools for identifying and genotyping Brucella isolates [3, 7–9].

The Qinghai-Tibetan Plateau (QTP) is the largest and highest plateau on Earth, with an area of 2.5 × 106 km2 and an average elevation of 4,000 m above sea level [10]. The QTP is an extensive pastoral and semi-pastoral area, and owing to poverty and bad hygiene, Brucella is highly endemic to this region among yaks (Bos grunniens) [11, 12] and humans [13]. It should be mentioned that, probably due to technical difficulties, most previous studies on Brucella in the QTP merely examined infection surveillance, without paying adequate attention to the study of taxonomic identification of Brucella species. In the present study we collected a considerable number of Brucella samples from Qinghai Province, (Table 1) which is located in the northeastern corner of the QTP and constitutes >25 % of the area of the plateau (Fig. 1). We used both MLVA as well as MLST methods to type these samples and determine the composition characteristics of Brucella in the plateau area.

Table 1 Geographic distribution of Brucella samples in Qinghai, China
Full size table
Fig. 1
figure 1

Geographic distribution of Brucella samples in Qinghai, China. QTP, Qinghai-Tibet Plateau; the dotted counties (NO. 1 ~ 13) correspond to the 13 counties (Locality ID 1 ~ 13) in Table 1. The pie charts showed the composition (the relative pie size corresponds to the number of strains) of the four branches (A, B, C, and E) of B. melitensis

Full size image

Methods

Ethics statement

This study is a retrospective investigation of our historical collection with modern typing methods. Therefore, the study does not involve the collection or reporting of patient data. No animal work was carried out with the obtained results.

Bacterial strains and DNA preparation

A total of 65 isolates were examined: 31 recovered from human, 15 from sheep (Ovis aries), 11 from blue sheep (Pseudois nayaur), 6 from yaks (Bos mutus grunniens), and 1 each from cattle (Bos primigenius taurus) and Tibetan gazelle (Procapra picticaudata). Bacterial strains were cultured on Trypticase soy agar containing 5 % sheep blood (BD Diagnostic Systems, China Ltd., China) at 37 °C for 48 h. Total genomic DNA was extracted using the DNeasy Blood & Tissue Kit (Qiagen, Germany) as per the manufacturer’s recommended protocol.

MLVA genotyping

MLVA was performed as described earlier [9]. Briefly, 16 primer pairs were designed and classified as belonging to one of the three panels: panel 1 (bruce06, bruce08, bruce11, bruce12, bruce42, bruce43, bruce45, and bruce55), panel 2A (bruce18, bruce19, and bruce21), and panel 2B (bruce04, bruce07, bruce09, bruce16, and bruce30). PCR amplifications were performed in 40 μL reaction volumes, 5 μL of these were loaded in to 2 % (panel 1) or 3 % (panels 2A and 2B) agarose gels containing 0.5 μg/ml of ethidium bromide, visualized under UV light, and photographed. Band intensities were estimated using BioNumerics version 5.1 (Applied Maths, Belgium) and were then converted to repeat units by following the published allele numbering system [7].

In order to improve the genotyping accuracy, PCR products were also directly sequenced after purification. The sequences were aligned and the numbers of repeat units were checked in MEGA version 5 [14] using B. melitensis 16 M genome sequence as a reference (GenBank accession number NC_003317.1 and NC_003318.1). Clustering analysis was based on the categorical coefficient and unweighted pair group method using arithmetic averages (UPGMA) method provided in BioNumerics. The resulting genotypes were compared using the web-based Brucella2012 MLVA database (http://mlva.u-psud.fr/).

MLST genotyping

Nine distinct genomic loci, including seven housekeeping genes (gap, aroA, glk, dnaK, gyrB, trpE, and cobQ), one outer membrane protein (omp25), and one intergenic fragment (int-hyp), were selected for MLST genotyping [15]. Similar to the MLVA process described, PCR amplifications were performed in 40 μL reaction volumes using primer sequences as previously described [3]. Sequences obtained from purified PCR products were aligned using MEGA program and verified by visualizing. MLST sequences (GenBank accession number AM694191 ~ AM695630) of the strains described by Whatmore et al. [3] were downloaded and a local BLAST database was built using makeblastdb program of BLAST+ program package version 2.2.31 [16]. The sequences were matched with the local database using blastn program of the BLAST+ program package.

The BLAST results were parsed using BLAST Parser program version 1.2.6 [17]. Distinct alleles identified at the nine selected loci were each given a numerical designation according to sequence of defined alleles. If the sequence was different from those defined previously, it was designated as a new allele. Each sequence type over all loci (ST) was predicted using web-based MLST service (BrucellaBase, http://59.99.226.203/brucellabase/mlst.html). Phylogenetic relationships of combined sequences were inferred using the Neighbor-Joining method in BrucellaBase.

We could not identify biovars within strains, because it was difficult to distinguish among them using either MLVA16 or MLST markers [3, 18, 19].

Findings

MLVA results

Using panel 1 markers, the present population clustered into eight known genotypes: 42 (1-5-3-13-2-2-3-2; N = 51), 43 (1-5-3-13-3-2-3-2; N = 6), 47 (3-4-2-13-4-2-3-3; N = 2), 28 (4-5-4-12-2-2-3-3; N = 2), 63 (1-5-3-13-2-3-3-2; N = 1), 36 (4-5-3-12-2-2-3-1; N = 1), 112 (4-5-3-12-2-2-3-3; N = 1), and 6 (2-3-6-10-4-1-5-2; N = 1). The Clustering analysis showed that the 65 isolates formed six main clusters (A ~ F). Cluster A had two genotypes (42 and 63); cluster B, C, E and F had a single genotype 42, 43, 47 and 6, respectively; cluster D had three genotypes (112, 36, and 28) (Fig. 2). According to Brucella2012 MLVA database and based on panel 1 markers we identified our samples as containing three species: B. melitensis (genotype 42, 43 and 47; cluster A, B, C and E), B. abortus (genotype 28, 36 and 112; cluster D) and B. suis (genotype 6; cluster F).

Fig. 2
figure 2

Dendrogram based on the MLVA genotyping assay showing relationships of the 65 Brucella isolates. ID: serial number for the 65 isolates; MLVA type: panel 1 and MLVA-16 genotypes; Host: the hosts from which the bacteria was isolated; Isolate: isolate name in the laboratory in which the DNA extraction was done; Year: the years when the strains were collected

Full size image

Based on a previous study [20], the B. melitensis strains were sub-grouped into “East Mediterranean” group (genotype 42 and 43) and “American” group (genotype 47). Considering all three MLVA panels, 34 (Bm01 ~ Bm34), 3 (Ba01 ~ Ba03), and 1 (Bs01) MLVA-16 genotypes were identified for B. melitensis, B. abortus and B. suis isolates respectively (Fig. 2). No genotypes completely matched any of the genotypes in the Brucella2012 MLVA database.

MLST results

A total of five known MLST genotypes were identified: ST7 (3-5-3-2-1-5-2-10-2; N = 2), ST8 (3-2-3-2-1-5-3-8-2; N = 57), ST2 (2-1-2-2-1-3-1-1-1; N = 2), ST5 (2-1-1-2-1-4-1-1-1; N = 2), ST14 (1-6-4-1-4-3-5-2-1; N = 1). The Neighbor-Joining clustering showed that the 65 isolates formed four main clusters – a, d, e and f. Of these, clusters a, e and f correspond to genotypes ST8, ST7 and ST14 respectively while cluster d corresponds to two genotypes, ST2 and ST5. According to Whatmore et al. [3], genotypes ST7 and ST8 belong to B. melitensis, ST2 and ST5 belong to B. abortus, and ST14 belongs to B. suis.

The gyrB sequence of strain Ma06 was different from any of known alleles (allele 1 ~ 6). Its sequence closely matched that of allele 1 (identical except for a di-nucleotide change of GC to AA on site 405 ~ 406 relative to the gyrB allele 1 sequence or on 2504 ~ 2505 sites relative to the ST8 sequence). Considering all MLST alleles, the strain Ma06 could be viewed as a mutant variant (3-2-3-2-?-5-3-8-2) of ST8 (3-2-3-2-1-5-3-8-2).

Discussion

In this study we used both MLVA and MLST methods to identify Brucella species in the east of the Qinghai-Tibet Plateau. Although there were some minor incongruences for e.g., in clustering results (Fig. 2 and Fig. 3), both methods showed a consistent conclusion that there were at least three Brucella species in the sample analyzed. Of the 65 isolates 60, 4, and 1 were respectively identified to B. melitensis, B. abortus, and B. suis, indicating that B. melitensis was a predominant species on the plateau. Interestingly however, when searching in the Brucella2012 MLVA database none of the genotypes found in our study were identical to any of the genotypes in the database. Based on MLST the ST8 seems to be the main ST type in the QTP region. Moreover, there was also a unique genotype (strain Ma06) which has not been reported anywhere before. These results demonstrated that the Brucella population found in the QTP region was very different from that in other regions. We attribute this to relatively isolated and special environment of the plateau. Extremely high altitudes make it difficult for lowland livestock breeds or wild animals to survive, thereby favoring only the endemic ones. Hence, there was a very limited breeds exchange between QTP and other regions, which may have consequently formed a unique local Brucella population.

Fig. 3
figure 3

Dendrogram based on the MLST genotyping assay showing relationships of the 65 Brucella isolates. ID: serial number for the 65 isolates; ST: MLST genotypes; Host: the hosts from which the bacteria was isolated. (Also see Fig. 2 for additional information)

Full size image

Based on MLVA-16, ten genotypes were shared by two or more host species. To elaborate further, four genotypes (Bm09, Bm19, Bm20, and Bm25) were shared between humans and sheep, and two (Bm08 and Ba03) were shared between humans and yaks (Fig. 2). Based on MLST, the ST8 type was also shared between humans and four other animals (sheep, yaks, blue sheep and Tibetan gazelle); the ST5 type was shared between humans and yaks (Fig. 3). Sheep and yaks are the main livestock on QTP and it is therefore not surprising that these animals pose a heavy zoonotic disease threat to humans. It should be noted that, all sheep and four out of six yaks were infected by B. melitensis, indicating that this bacterial species should be paid special attention to in both host species. It is well known that different bacterial species need different vaccine strains. For instance, there are three vaccine strains M5, S19 and S2, which are used to immunize animals in China for B. melitensis, B. abortus, and B. suis, respectively [21]. Because yaks could be infected by either B. melitensis or B. abortus, we suggest based on our study that both the B. melitensis type (M5) and B. abortus type vaccines (S19) should be tried in this animal.

The blue sheep were infected by all three Brucella species including B. suis, which is generally carried by pigs [1, 22]. More importantly, this animal shared Brucella genotypes with human (Bm07, Bm15 and Bm25), yaks (Bm06), and Tibetan gazelle (Bm01), indicating this animal is an important natural repertory for Brucella. Since there is obvious spatial and diet overlap between blue sheep and domestic livestock [23], we suggest that this animal is also an important infection source of Brucella in humans.

Additionally, due to high genetic diversity of B. melitensis, we also discuss the geographic distribution features of the strains. Figure 1 showed that 7 counties (locality ID: 2, 3, 5, 8, 9, 10, and 12) were dominated by A branch strains; 3 counties (locality ID: 1, 4, and 6) were dominated by B branch strains; 3 counties (locality ID: 7, 11, and 13) contained only C branch strains; and the E branch genotypes appeared only in 1 county (locality ID: 2). These results showed that the B. melitensis prevalence in the QTP region might have a considerable regional characteristic i.e., there might be genetic variations among different regions.

Our results for the first time elucidated the composition of species and genotypes of Brucella samples in the QTP region. We also presented the host- as well as geographic distributions of the species and genotypes. These results may have some implications for the future disease control programmes in QTP. First, since B. melitensis was the predominant species in the study area, special attention should be paid on this species in brucellosis control programs such as livestock vaccination. Second, the genotypes of Brucella in the QTP region were very different from other regions, but whether the genetic difference may result in different vaccination efficiencies should be elucidated in the further studies. Third, since there were extensive genotype-sharing events between humans and animals, brucellosis surveillance should be regularly executed on both livestock (sheep and yaks) and wild ungulates (blue sheep).

It should be noted that, as mentioned above, none of the genotypes found in our study were identical to any of the genotypes in the Brucella2012 database, in order to prevent over-interpreting our results, we did not compare our strains with those from other studies. This might limit our understanding of genetic relationships between the Brucella populations from QTP and from other regions. Moreover, because of imbalance of sample sizes among different counties and among different hosts, in this study, we were not able to do a detail epidemiological investigation. We suggest that the accumulation of more samples will enable us to further elucidate the genetic characteristics of Brucella species in QTP.

Conclusions

Our study drew three main conclusions: (i) there were at least three Brucella (B. melitensis, B. abortus and B. suis) species in the east of QTP and B. melitensis was the predominant species in the area studied; (ii) the Brucella population in the QTP region was very different from other regions probably due to the unique geographical characteristics e.g., extremely high altitude in QTP; and (iii) there were extensive genotype-sharing events between humans and animals; sheep, yaks and blue sheep were important zoonotic hosts of brucellosis to humans in the area studied.

Abbreviations

MLST:

multi locus sequence typing

MLVA:

multi-locus variable-number tandem-repeat analysis

QTP:

Qinghai-Tibet Plateau

References

  1. Atluri VL, Xavier MN, de Jong MF, den Hartigh AB, Tsolis RM. Interactions of the human pathogenic Brucella species with their hosts. Annu Rev Microbiol. 2011;65:523–41.

    Article  CAS  PubMed  Google Scholar 

  2. Pappas G, Papadimitriou P, Akritidis N, Christou L, Tsianos EV. The new global map of human Brucellosis. Lancet Infect Dis. 2006;6:91–9.

    Article  PubMed  Google Scholar 

  3. Whatmore AM, Perrett LL, MacMillan AP. Characterisation of the genetic diversity of Brucella by multilocus sequencing. BMC Microbiol. 2007;7:34.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Kansiime C, Rutebemberwa E, Asiimwe BB, Makumbi F, Bazira J, Mugisha A. Annual trends of human brucellosis in pastoralist communities of south-western Uganda: a retrospective ten-year study. Infec Dis Poverty. 2015;4:39.

    Article  Google Scholar 

  5. Ducrotoy MJ, Ammary K, Lbacha HA, Zouagui Z, Mick V, Prevost L, Bryssinckx W, Welburn SC, Benkirane A. Narrative overview of animal and human brucellosis in Morocco: intensification of livestock production as a driver for emergence? Infec Dis Poverty. 2015;4:57.

    Article  Google Scholar 

  6. Garin-Bastuji B, Mick V, Le Carrou G, Allix S, Perrett LL, Dawson CE, et al. Examination of taxonomic uncertainties surrounding Brucella abortus bv. 7 by phenotypic and molecular approaches. Appl Environ Microbiol. 2014;80(5):1570–9.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Le Flèche P, Jacques I, Grayon M, Al Dahouk S, Bouchon P, Denoeud F, et al. Evaluation and selection of tandem repeat loci for a Brucella MLVA typing assay. BMC Microbiol. 2006;6:9.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Chen Y, Zhen Q, Wang Y, Xu J, Sun Y, Li T, et al. Development of an extended multilocus sequence typing for genotyping of Brucella isolates. J Microbiol Methods. 2011;86(2):252–4.

    Article  CAS  PubMed  Google Scholar 

  9. Di D, Cui B, Wang H, Zhao H, Piao D, Tian L, et al. Genetic polymorphism characteristics of Brucella canis isolated in China. PLoS One. 2014;9(1):e84862.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Wu T. The Qinghai-Tibetan plateau: how high do Tibetans live? High Alt Med Biol. 2001;2:489–99.

    Article  CAS  PubMed  Google Scholar 

  11. Wiener G, Han J, Long R. The yak. 2nd ed. Bangkok: RAP publication; 2003.

    Google Scholar 

  12. Lang X, Qu H, Bu Z, Yang Y, Sun C, Li X, et al. Seroprevalence of Brucella infection in yaks (Bos grunniens) on the Qinghai-Tibet plateau of China. Trop Anim Health Prod. 2011;43:305–6.

    Article  Google Scholar 

  13. Xue H. Analysis on infection and the related factor of brucellosis in high-risk population in Qinghai Province of 2006 to 2010. Taiyuan, Shanxi Province, China: Master thesis of Shanxi Medical University; 2012.

  14. Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011;28(10):2731–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Chen Y, Ke Y, Wang Y, Yuan X, Zhou X, Jiang H, et al. Changes of predominant species/biovars and sequence types of Brucella isolates, Inner Mongolia. China BMC Infect Dis. 2013;13:514.

    Article  PubMed  Google Scholar 

  16. Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, et al. BLAST+: architecture and applications. BMC Bioinformatics. 2009;10:421.

    Article  PubMed  PubMed Central  Google Scholar 

  17. Marco C, Roberta B. BLAST Parser. BITS Conference. Societa di Bioinformatica Italiana. Bologna. Societa di Bioinformatica Italiana Bologna Italy. 2006;5:28–9.

    Google Scholar 

  18. Jiang H, Fan M, Chen J, Mi J, Yu R, Zhao H, et al. MLVA genotyping of Chinese human Brucella melitensis biovar 1, 2 and 3 isolates. BMC Microbiol. 2011;11:256.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Jiang H, Wang H, Xu L, Hu G, Ma J, Xiao P, et al. MLVA genotyping of Brucella melitensis and Brucella abortus isolates from different animal species and humans and identification of Brucella suis vaccine strain s2 from cattle in China. PLoS One. 2013;8(10):e76332.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Al Dahouk S, Le Flèche P, Nöckler P, Jacques I, Grayon M, Scholz HC, et al. Evaluation of Brucella MLVA typing for human brucellosis. J Microbiol Methods. 2007;69:137–45.

    Article  CAS  PubMed  Google Scholar 

  21. Shang D, Xiao D, Yin J. Epidemiology and control of brucellosis in China. Vet Microbiol. 2002;90:165–82.

    Article  Google Scholar 

  22. Burniston S, Okello AL, Khamlome B, Inthavong P, Gilbert J, Blacksell SD, Allen J, Welburn SC. Cultural drivers and health-seeking behaviours that impact on the transmission of pig-associated zoonoses in Lao People’s Democratic Republic. Infec Dis Poverty. 2015;4:11.

    Article  Google Scholar 

  23. Mishra C, Van Wieren SE, Ketner P, Heitkonig IMA, Prins HHT. Competition between domestic livestock and wild bharal Pseudois nayaur in the Indian Trans-Himalaya. J Appl Ecol. 2004;41(2):344–54.

    Article  Google Scholar 

Download references

Acknowledgments

This study was supported by the Science and Technology Plan of Qinghai Province (NO. 2013-Z-749) and the Youth Innovation Promotion Association of Chinese Academy of Sciences (NO. 2015352).

Author information

Author notes

    Authors and Affiliations

    1. Qinghai Institute for Endemic Disease Prevention and Control, Xining, 811602, Qinghai, China

      Jun-Ying Ma, Hu Wang, Xue-Fei Zhang, Li-Qing Xu, Gui-Ying Hu & Yu-Min Qin

    2. State Key Laboratory for Infectious Disease Prevention and Control, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, 102206, China

      Hai Jiang, Hong-Yan Zhao, Dong-Ri Piao & Bu-Yun Cui

    3. Key Laboratory of Adaptation and Evolution of Plateau Biota, Northwest Institute of Plateau Biology, Chinese Academy of Sciences, Xining, 810008, Qinghai, China

      Fang Zhao & Gong-Hua Lin

    Authors
    1. Jun-Ying Ma
      View author publications

      You can also search for this author in PubMed Google Scholar

    2. Hu Wang
      View author publications

      You can also search for this author in PubMed Google Scholar

    3. Xue-Fei Zhang
      View author publications

      You can also search for this author in PubMed Google Scholar

    4. Li-Qing Xu
      View author publications

      You can also search for this author in PubMed Google Scholar

    5. Gui-Ying Hu
      View author publications

      You can also search for this author in PubMed Google Scholar

    6. Hai Jiang
      View author publications

      You can also search for this author in PubMed Google Scholar

    7. Fang Zhao
      View author publications

      You can also search for this author in PubMed Google Scholar

    8. Hong-Yan Zhao
      View author publications

      You can also search for this author in PubMed Google Scholar

    9. Dong-Ri Piao
      View author publications

      You can also search for this author in PubMed Google Scholar

    10. Yu-Min Qin
      View author publications

      You can also search for this author in PubMed Google Scholar

    11. Bu-Yun Cui
      View author publications

      You can also search for this author in PubMed Google Scholar

    12. Gong-Hua Lin
      View author publications

      You can also search for this author in PubMed Google Scholar

    Corresponding authors

    Correspondence to Bu-Yun Cui or Gong-Hua Lin.

    Additional information

    Competing interests

    The authors declare that they have no competing interests.

    Authors’ contributions

    JYM, HW, BYC and GHL contributed to the design of the study. JYM, BYC and GHL collected the data and wrote the paper. JYM, XFZ, LQX, GYH, HJ, FZ, HYZ, DRP, YMQ and GHL analyzed the data. All authors read and approved the final paper.

    Additional file

    Additional file 1:

    Multilingual abstracts in the six official working languages of the United Nations. (PDF 350 kb)

    Rights and permissions

    Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

    Reprints and permissions

    About this article

    Check for updates. Verify currency and authenticity via CrossMark

    Cite this article

    Ma, JY., Wang, H., Zhang, XF. et al. MLVA and MLST typing of Brucella from Qinghai, China. Infect Dis Poverty 5, 26 (2016). https://doi.org/10.1186/s40249-016-0123-z

    Download citation

    • Received:

    • Accepted:

    • Published:

    • DOI: https://doi.org/10.1186/s40249-016-0123-z

    Keywords

    Infectious Diseases of Poverty

    ISSN: 2049-9957

    Contact us