Identification of Listeria monocytogenes Virulence Factors in Women With Abortion by Polymerase Chain Reaction

AUTHORS

Gita Eslami 1 , Hossein Goudarzi 2 , Elnaz Ohadi 3 , * , Arezou Taherpour 2 , Bita Pourkaveh 1 , Soudabeh Taheri 2

1 Infectious Diseases and Tropical Medicine Research Center, Shahid Beheshti University of Medical Sciences, Tehran, IR Iran

2 Department of Microbiology, Shahid Beheshti University of Medical Sciences, Tehran, IR Iran

3 Department of Microbiology, International Branch of Shahid Beheshti University of Medical Sciences, Tehran, IR Iran

How to Cite: Eslami G, Goudarzi H, Ohadi E, Taherpour A, Pourkaveh B, et al. Identification of Listeria monocytogenes Virulence Factors in Women With Abortion by Polymerase Chain Reaction, Arch Clin Infect Dis. 2014 ; 9(3):e19931. doi: 10.5812/archcid.19931.

ARTICLE INFORMATION

Archives of Clinical Infectious Diseases: 9 (3); e19931
Published Online: June 25, 2014
Article Type: Research Article
Received: September 15, 2013
Revised: February 2, 2014
Accepted: May 20, 2014
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Abstract

Background: Listeria monocytogenes, as one of the foodborne pathogens, is a causative agent of listeriosis. The transfer of L. monocytogenes bacteremia in pregnant women occurs as self-limited flu-like symptoms, but it may result in abortion, stillbirth or premature birth of the infected baby. One of the best methods for detection of this bacterium is polymerase chain reaction (PCR).

Objectives: The purpose of this study was detection of virulence factors (hlyA and plcA) of L. monocytogenes in women with abortion, using PCR.

Patients and Methods: In this pilot and cross-sectional study, 96 patients with abortion admitted in educational university, Tehran, Iran were surveyed for L. monocytogenes by PCR and culture methods. Some variants like age, occupation, history of abortion and education were considered for all patients. Vaginal swabs and secretions were transferred to trypticase soy broth as the transport media and then all the samples were transferred to a microbiology laboratory. The tubes were incubated in 4 ºC and the specimens were cultured on PALCAM media. The isolates were verified by Gram staining, catalase and oxidase test, methyl red-Voges-Proskauer (MR-VP), sugar fermentations and motility in 20-25ºC. Then, PCR was performed for the extracted DNAs. Data were analyzed by SPSS software version 17, and χ2 (Chi-square test).

Results: Out of 96 samples, 16 isolates of L. monocytogenes by PCR (plcA and hlyA) and four isolates by culture were identified. There was a significant difference between PCR and culture methods (P = 0.003). The results of this study showed that PCR was more sensitive and specific than culture method. There was also a significant association between the bacteria and hlyA and plcA genes and human abortion and between patients with abortion precedence and education.

Conclusions: Based on our study, plcA and hlyA played a key role in the virulence determination of L. monocytogenes. Data analysis also showed that L. monocytogenes could be a causative agent of abortion in pregnant women.

Keywords

Listeria monocytogenes Abortion Polymerase Chain Reaction Culture

Copyright © 2014, Infectious Diseases and Tropical Medicine Research Center. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.

1. Background

Listeria monocytogenes, a bacterium that causes foodborne infections, can result in abortion and diseases as severe as encephalomeningitis, septicemias and gastroenteritis. It is a facultative intracellular and Gram-positive bacterium, presented in pregnant women by flu-like symptoms (1-3). Along with the occurrence of listeriosis in adults, it is especially important in fetuses, since around 40% of all cases are pregnancy-related, where the disease can cause miscarriage, premature birth, stillbirth, and neonatal disease (2, 4). The incidence of listeriosis among pregnant women is 17 times as high as the general population (12 per 100000 vs. 0.7 per 100000, respectively) (5).

L. monocytogenes has six basic virulence genes including prfA, plcA, hlyA, mpl, actA, and plcB, located together in one virulence gene cluster between the house keeping genes idh and prs (6). L. monocytogenes is identified by selective enrichments and biochemical analyses. One of the best instruments that has a tremendous potential for detection of foodborne pathogens is polymerase chain reaction (PCR), and therefore it has been one of the most sought-after methods in food microbiology in recent years(7-9).

2. Objectives

The objective of the present study was detecting the virulence-associated gene(s) in L. monocytogenes by PCR and culture methods among women with abortion. Finally, we compared the two results.

3. Patients and Methods

3.1. Samples Collection

In this pilot and cross-sectional study, a total of 96 samples including vaginal swabs were collected by convenience samplings method from patients with spontaneous abortions who had been admitted to educational medical centers of Tehran, Iran, during June 2012 to May 2013. All the specimens were transferred on ice to the Microbiology Research Laboratory of Shahid Beheshti University of Medical Sciences.

3.2. Inclusion and Exclusion Criteria

Inclusion criteria was the swab of a sample of abortion under 20 weeks of pregnancy, and exclusion criteria was the swab of a sample of pregnancy tissues more than 20 weeks of pregnancy.

3.3. Enrichment, Culturing, and Morphological and Biochemical Identification

Briefly, the vaginal swabs were placed in 10 mL tryptic soy broth with yeast extract (TSBYE); the samples were incubated at 4°C. After a one-week period or a one to three month period of incubation, aliquots from the enrichment broth (TSBYE) were streaked onto PALCAM agar (Merck, Germany) and blood agar (Merck, Germany) and the plates were incubated at 37°C for 24 to 48 hours. Green shiny colonies with diffused black shadows around them on PALCAM agar and yellow small colonies with ß-hemolysis on blood agar were suspected to be Listeria. The isolates were confirmed by Gram staining, catalase reaction, oxidase test, tumbling motility at 20-25ºC, methyl red-Voges Proskauer (MR-VP) tests, and fermentation of sugars (xylose, rhamnose and mannitol). All the biochemically characterized isolates were tested for haemolysis on sheep blood agar.

3.4. DNA Extraction

DNA extraction was performed by AccuPrepgenomic DNA extraction kit (Bioneer Co., Korea). After one week, the vaginal swab specimens with TSBYE were incubated at 4°C; then 20 μL of proteinase K and 200 μL of binding buffer were added to 200 μL of samples; after mixing, they were incubated at 60°C for 20 minutes; 100 μL of isopropanol was added to the mixtures. The lysates were centrifuged at 8000 rpm for one minute; washing buffer one and then two were added to the tubes, respectively. After the centrifuge, 200 μL of the elution buffers were added and the final mixture was centrifuged at 8000 rpm for one minute. The eluted genomic DNA was stored at -20°C for further analyses.

3.5. Polymerase Chain Reaction

The PCR was standardized for detecting two virulence associated genes of L. monocytogenes, namely plcA, hlyA, using primer pairs of 5'-ATCAGT GAAGGGAAAATGCAAGAAG-3' and 5'-TTGTATAAGCAATGGGAACTCCTGG-3' specific for hlyA and 5'-ATGTTAAGTTGAGTACGAATTGCTC-3' and 5'-TACGATGAGCTATAACGGAGACATG-3'specific for plcA. The specificity of the standardized PCR was tested by screening the standard strain of L. monocytogenes (ATCC 7644). PCR was performed in a final volume of 25 μL, containing 12 μL PCR master mix, 8 vμL double distilled water (DDW), 1 μL (each) primer targeting the plcA or hlyA gene and 3 μL of the template DNA. The amplifications were carried out in master cycler (Eppendorf Co., Germany) using the following program for hlyA: 95°C for one minute, followed by 40 cycles (95°C for 30 seconds, 59 °C for 35 seconds, and 72°C for 30 seconds) and 72°C for five minutes; the amplification program for plcA was 95°C for one minute, followed by 40 cycles (95°C for 30 seconds,51°C for 35 seconds, and 72°C for 30 seconds) and 72°C for five minutes. The PCR products bands were analyzed by electrophoresis in a 1.5% agarose gel at 95 V for 45 minutes in Tris-Borate-ethylenediaminetetraacetic acid (TBE) 1X containing ethidium bromide under UV irradiation. The sequencing method was performed by Bioneer Company (Korea) and then the sequences were analyzed with Chromas 1.45 software and BLAST in NCBI.

3.6. Data Analysis:

All data were compiled, and analysis was done using spss version 17 and for survey of sig­nificance, χ2 (Chi-square test) was calculated. Minimal level of significance was considered P < 0.05.

4. Results

Among 96 samples from spontaneous abortions, four specimens were positive for L. monocytogenes by microbiological tests. The standardized PCR allowed amplification of virulence-associated genes of L. monocytogenes, namely plcA and hlyA, to 659 and 451 bp PCR products, respectively. Among 96 samples, L. monocytogenes was found in 16 samples entailing plcA and hlyA genes according to the PCR results (Figures 1 and 2).

Figure 1. Polymerase Chain Reaction Products of hlyA gene (451 bp) on 1.5% Agarose Gel Stained With Ethidium Bromide
Polymerase Chain Reaction Products of hlyA gene (451 bp) on 1.5% Agarose Gel Stained With Ethidium Bromide

Lane 1, positive control; lanes 2-6 and 8, positive samples; lanes 7 and 9, negative control; Lane M, 50-bp PCR marker.

Figure 2. Polymerase Chain Reaction Products of plcA Gene (659 bp) on 1.5% Agarose Gel Stained With Ethidium Bromide
Polymerase Chain Reaction Products of plcA Gene (659 bp) on 1.5% Agarose Gel Stained With Ethidium Bromide

Lane 1, positive control; lanes 2-8, positive samples; lane 9, negative control; Lane M, 100-bp PCR marker.

Statistically, there was a significant difference between these two methods (P = 0.003). This study showed that PCR was more sensitive and specific than culture method.

The average age of the 96 women was 30.9 ± 4.7 years old and the average age of patients with positive L. monocytogenes PCR results was 33.5 ± 7.2 years old. Of 96 samples, 27 patients (28.1%) were low educated, 53 (55.2%) had a high school diploma and 16 (16.7%) had a college degree. High school graduates and low-educated patients had the highest incidence of Listeria compared with higher educated ones (11, 68.8%). Therefore, there was a significant association between patients positive forListeria and control samples regarding education; 95% CI [2.3-85.7 OR=12.2] (P = 0.00).

Of 96 patients, 12 (12.5%) had more than one abortion before and 84 (87.5%) did not have any abortion history. Of 16 patients positive for L. monocytogenes, 6 (37.5%) had abortion precedent. There was a significant association between patients with abortion precedence and with non-abortion precedence; 95% CI [1.7-33.5 OR=74] (P =0.001).

Analysis of all the samples indicates that of 16 patients positive for L. monocytogenes, 11 (68.8%) and 5 (31.2%) were housewives and employed women, respectively. Hence, there was no significant association between the housewives and the employed women (P = 0.9). The investigation of contraception methods also showed that there was no significant association between women with positive and negative Listeria regarding the contraception methods (Table 1). We did not encounter any missing value, either.

Table 1. Frequency of Listeria monocytogenes Based on the Research Variables a,b
VariablesPrevalence of L. monocytogenes by PCRPrevalence of L. monocytogenes by Culture
PositiveNegativeTotalPositiveNegativeTotal
Education
Low level of education3242722527
High school diploma 11425325153
Higher than diploma2141601616
Total16809649296
Age
Lower than 20 years011011
21-30 Years8334133841
31-41 Years8465415354
Total16809649296
Abortion precedence
Abortion precedence661221012
Non-abortion Precedence10748428284
Total16809649296
Job
Housewife11667737477
Employed 5141911819
Total16809649296
Contraception methods
Natural7273423234
Other methods9536226062
Total16809649296

aAbbreviation: PCR, polymerase chain reaction.

bData are presented as No.

5. Discussion

Few human listeriosis cases have been reported in Iran. This can be due to imperfect identification or isolation methods, lack of awareness, and low incidence rate in some regions. Approximately, one-third of reported human listeriosis is associated with pregnancy, causing spontaneous abortions, especially in the second or third trimester (10).

In the present study, 16 and four isolates of L. monocytogenes were recovered from human abortion cases by PCR and culture, respectively. The rate of L. monocytogenes identified by PCR was 16.7%. The result of the used methods as well as the data analysis showed that L. monocytogenes can be a causative agent of abortion in pregnant women.

A number of factors are involved in manifestation of L. monocytogenes virulence. Detection of only one virulence-associated gene by PCR is not always sufficient to identify L. monocytogenes(11, 12). Moreover, two genes (plcA and hlyA) were investigated in our study. L. monocytogenes phospholipases are essential determinants of pathogenicity and thus, we investigated them as well (5). plcA and hlyA existed in all the positive cases (16). In a study by Kaur et al. the prevalence of L. monocytogenes in India reported four isolates from 305 samples comprising blood, urine, and placental bits, faecal and vaginal swabs that were collected from 61 patients with spontaneous abortion samples. Another result of this research was that plcA and its expression had key roles in virulence determination of L. monocytogenes (5).

Shayan et al. reported 36 isolates of L. monocytogenes in Iran with PCR method and 7 isolates with culture, among 100 vaginal samples. In accordance with this study, PCR was faster, more sensitive and more specific than culture method for identifying L. monocytogenes in vaginal swabs. Because of some factors like the number of samples and country similarity, the results of this research were similar to our results (13).

In a research study conducted by Kargar et al. in Iran, out of 311 samples (urine, blood, placenta and cervix), no positive cases were detected by culture method, but 10.28% prevalence for L. monocytogenes by PCR for hlyA was identified. There was similarity between Kargar’s research and our study in abortion precedence. This similarity can be related to country conditions and similar applied methods (14). Based on the survey of Ahmed et al., 71 examined seafood samples, 20 (28.2%) were identified with L. monocytogenes, 15 (75%) of which were confirmed as virulent strains. In addition, of 50 human stool samples, only 1 (2%) was identified with virulent L. monocytogenes (15).

The results of the study of Chao et al. in china showed that of 548 samples, 32 strains (5.8%) were isolated from pre-prepared foods in markets and the average prevalence was 13.06% by PCR method for hlyA. The study showed that the prevalence of L. monocytogenes in pre-prepared foods in markets was significantly higher than those in cooked foods of hotels and restaurants. The difference of results between our study and that of Chao’s can be explained by samples differences (16).

Based on Jahangirsisakht et al. study in Iran, among 311 samples collected from 107 pregnant women (including urine, blood, placenta and cervix swab), 190 specimens were from pregnant women with a history of abortion and 120 from cases with normal delivery. Among 107 pregnant women, L. monocytogenes hlyA gene was detected in 11 (10.28%), with the highest frequency in the age group of 26-30 years old. The mean age of participants was 26.7 years old and almost 64% of positive samples were taken from cervix. The results of this survey were similar to the outcomes of our study; in addition, the samples and the studied genes were alike in both (17).

The result of Goudarzi et al. study showed that out of a total of 87 blood samples, 12 were detected positive for L. monocytogenes using both culture and PCR methods. The results also showed a significant statistical relationship between recurrent abortions and level of education using PCR (P < 0.05). Because of several factors like age, positive cases and education, the results of this study and our study had more similarity compared to other researches (18).

Acknowledgements

Footnotes

References

  • 1.

    Pust S, Morrison H, Wehland J, Sechi AS, Herrlich P. Listeria monocytogenes exploits ERM protein functions to efficiently spread from cell to cell. EMBO J. 2005; 24(6) : 1287 -300 [DOI][PubMed]

  • 2.

    Autio T. Tracing the sources of Listeria monocytogenes contamination and listeriosis using molecular tools. 2003;

  • 3.

    Neuhaus K, Satorhelyi P, Schauer K, Scherer S, Fuchs TM. Acid shock of Listeria monocytogenes at low environmental temperatures induces prfA, epithelial cell invasion, and lethality towards Caenorhabditis elegans. BMC Genomics. 2013; 14 : 285 [DOI][PubMed]

  • 4.

    World health organization . International Food Safety Authorities Network (INFOSAN) 2008;

  • 5.

    Kaur S, Malik SV, Vaidya VM, Barbuddhe SB. Listeria monocytogenes in spontaneous abortions in humans and its detection by multiplex PCR. J Appl Microbiol. 2007; 103(5) : 1889 -96 [DOI][PubMed]

  • 6.

    Morobe IC, Obi CL, Nyila MA, Matsheka MI, Gashe BA. Molecular Characterization and Serotyping of Listeria monocytogenes with a Focus on Food Safety and Disease Prevention. BiochemTest. : 978 -53

  • 7.

    Rawool DB, Malik SVS, Barbuddhe SB, Shakuntala I, Aurora R. A multiplex PCR for detection of virulence associated genes in Listeria monocytogenes. Int J Food Saf. 2007; 9 : 56 -62

  • 8.

    Rawool DB, Malik SV, Shakuntala I, Sahare AM, Barbuddhe SB. Detection of multiple virulence-associated genes in Listeria monocytogenes isolated from bovine mastitis cases. Int J Food Microbiol. 2007; 113(2) : 201 -7 [DOI][PubMed]

  • 9.

    Paziak-Domanska B, Boguslawska E, Wieckowska-Szakiel M, Kotlowski R, Rozalska B, Chmiela M, et al. Evaluation of the API test, phosphatidylinositol-specific phospholipase C activity and PCR method in identification of Listeria monocytogenes in meat foods. FEMS Microbiol Lett. 1999; 171(2) : 209 -14 [PubMed]

  • 10.

    Coordinating Center for Infectious Diseases / Division of Bacterial and Mycotic Diseases . Listeriosis. 2005;

  • 11.

    Portnoy DA, Chakraborty T, Goebel W, Cossart P. Molecular determinants of Listeria monocytogenes pathogenesis. Infect Immun. 1992; 60(4) : 1263 -7 [PubMed]

  • 12.

    Vazquez-Boland JA, Kuhn M, Berche P, Chakraborty T, Dominguez-Bernal G, Goebel W, et al. Listeria pathogenesis and molecular virulence determinants. Clin Microbiol Rev. 2001; 14(3) : 584 -640 [DOI][PubMed]

  • 13.

    Shayan R. Isolation and identification of Listeria monocytogenes in Vaginal samples using PCR method. Modares J Med Sci. 2010; 12 : 51 -8

  • 14.

    Kargar M. Comparing culture and molecular methods for detection of Listeria monocytogenes in Pregnant women. Armaghane Danesh, Journal of medical science Yasuj Medical University. 2012; 17

  • 15.

    Ahmed HA, Hussein MA, El-Ashram AM. Seafood a potential source of some zoonotic bacteria in Zagazig, Egypt, with the molecular detection of Listeria monocytogenes virulence genes. Vet Ital. 2013; 49(3) : 299 -308 [DOI][PubMed]

  • 16.

    Chao G, Deng Y, Zhou X, Xu Q, Qian X, Zhou L, et al. Prevalence of Listeria monocytogenes in delicatessen food products in China. Food control. 2006; 17(12) : 971 -4

  • 17.

    Jahangirsisakht A, Kargar M, Mirzaee A, Akbartabar Toori M, Aramesh SH, Mohamadkhani N, et al. Assessing Listeria monocytogenes hly A gene in pregnant women with spontaneous abortion using PCR method in Yasuj, south west of Iran. Afr J Microbiol Res. 2013; 7(33) : 4257 -60

  • 18.

    Goudarzi E. urvey of Polymerase Chain Reaction Efficiency in the Detection of Mycoplasma, Listeria and Brucella in Culture Negative Samples Obtained from Women with Abortion. J Mazand Univ Med Sci. 2013; 23(105) : 61 -9

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