Hostname: page-component-78c5997874-94fs2 Total loading time: 0 Render date: 2024-11-10T22:00:44.338Z Has data issue: false hasContentIssue false

2013 multistate outbreaks of Cyclospora cayetanensis infections associated with fresh produce: focus on the Texas investigations

Published online by Cambridge University Press:  13 April 2015

F. ABANYIE*
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
R. R. HARVEY
Affiliation:
Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, GA, USA National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
J. R. HARRIS
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
R. E. WIEGAND
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
L. GAUL
Affiliation:
Texas Department of State Health Services, Austin, TX, USA
M. DESVIGNES-KENDRICK
Affiliation:
Fort Bend County Health & Human Services, Rosenberg, TX, USA
K. IRVIN
Affiliation:
United States Food and Drug Administration, College Park, MD, USA
I. WILLIAMS
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
R. L. HALL
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
B. HERWALDT
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
E. B. GRAY
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
Y. QVARNSTROM
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
M. E. WISE
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
V. CANTU
Affiliation:
Texas Department of State Health Services, Austin, TX, USA
P. T. CANTEY
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
S. BOSCH
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
A. J. DA SILVA
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA United States Food and Drug Administration, College Park, MD, USA
A. FIELDS
Affiliation:
United States Food and Drug Administration, College Park, MD, USA
H. BISHOP
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
A. WELLMAN
Affiliation:
United States Food and Drug Administration, College Park, MD, USA
J. BEAL
Affiliation:
United States Food and Drug Administration, College Park, MD, USA
N. WILSON
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA Epidemic Intelligence Service, Centers for Disease Control and Prevention, Atlanta, GA, USA
A. E. FIORE
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
R. TAUXE
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
S. LANCE
Affiliation:
National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA United States Food and Drug Administration, College Park, MD, USA
L. SLUTSKER
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
M. PARISE
Affiliation:
Center for Global Health, Division of Parasitic Diseases and Malaria, Centers for Disease Control and Prevention, Atlanta, GA, USA
*
*Author for correspondence: F. Abanyie, MD, MPH, Medical Epidemiologist, Parasitic Diseases Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, 1600 Clifton Rd, Mail Stop A-06, Atlanta, GA 30333, USA.(Email: why6@cdc.gov)
Rights & Permissions [Opens in a new window]

Summary

The 2013 multistate outbreaks contributed to the largest annual number of reported US cases of cyclosporiasis since 1997. In this paper we focus on investigations in Texas. We defined an outbreak-associated case as laboratory-confirmed cyclosporiasis in a person with illness onset between 1 June and 31 August 2013, with no history of international travel in the previous 14 days. Epidemiological, environmental, and traceback investigations were conducted. Of the 631 cases reported in the multistate outbreaks, Texas reported the greatest number of cases, 270 (43%). More than 70 clusters were identified in Texas, four of which were further investigated. One restaurant-associated cluster of 25 case-patients was selected for a case-control study. Consumption of cilantro was most strongly associated with illness on meal date-matched analysis (matched odds ratio 19·8, 95% confidence interval 4·0–∞). All case-patients in the other three clusters investigated also ate cilantro. Traceback investigations converged on three suppliers in Puebla, Mexico. Cilantro was the vehicle of infection in the four clusters investigated; the temporal association of these clusters with the large overall increase in cyclosporiasis cases in Texas suggests cilantro was the vehicle of infection for many other cases. However, the paucity of epidemiological and traceback information does not allow for a conclusive determination; moreover, molecular epidemiological tools for cyclosporiasis that could provide more definitive linkage between case clusters are needed.

Type
Original Papers
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © Cambridge University Press 2015

INTRODUCTION

Cyclospora cayetanensis is the protozoan parasite that causes cyclosporiasis. Cyclosporiasis is characterized by profuse watery diarrhoea; anorexia, fatigue, weight loss, nausea, flatulence, abdominal cramping, myalgia, vomiting, and low-grade fever may also occur [Reference Herwaldt1]. Symptoms typically begin an average of 7 days (range 2–14 days) after ingestion of the infective form of the parasite and, if infection is left untreated, may last weeks to months with remitting and relapsing symptoms [Reference Herwaldt1]. Cyclosporiasis occurs most commonly in tropical and subtropical regions. In the United States, at least one third of non-outbreak-associated cyclosporiasis cases have been associated with international travel [Reference Hall, Jones and Herwaldt2]. Since the mid-1990s cyclosporiasis outbreaks have been linked to imported fresh produce, including raspberries, basil, snow peas, and mesclun lettuce [Reference Herwaldt1, 3, Reference Herwaldt and Ackers4]. C. cayetanensis is not directly transmitted from one person to another; an infected person sheds unsporulated oocysts in the faeces, which are non-infective. These oocysts do not multiply outside the human host and require days to weeks in the environment to become infective [Reference Ortega5]. Infection is seasonal, and the time of year and environmental conditions responsible for transmission vary around the world. In the United States, most of the reported cases have occurred during May–August, peaking in June and July [Reference Herwaldt1, Reference Hall, Jones and Herwaldt2].

The 2013 multistate outbreaks of cyclosporiasis contributed to the highest annual number of cyclosporiasis cases in the United States since 1997. Cyclosporiasis has been a nationally notifiable disease in the United States since 1999 [Reference Hall, Jones and Herwaldt2]. At the time of writing this paper, cases of cyclosporiasis are reportable in 40 states, the District of Columbia, and New York City, which notify the Centers for Disease Control and Prevention (CDC) of cases via the Nationally Notifiable Diseases Surveillance System [6]. On 28 June 2013, CDC was notified of two laboratory-confirmed cases of cyclosporiasis in Iowa residents who became ill in June and did not have a history of international travel during the 14 days before illness onset. After additional cases were reported from other states, collaborative epidemiological and traceback investigations were conducted by CDC, state and local public health officials, and the U.S. Food and Drug Administration (FDA). Three states reported the majority of cases: Texas, Iowa, and Nebraska. The implicated food vehicle in the restaurant-associated cases in Iowa and Nebraska was a prepackaged salad mix, produced by a supplier in Guanajuato, Mexico, containing iceberg and romaine lettuce, red cabbage, and carrots [7]. We describe the investigations in Texas, the state with the highest number of reported cases during the investigation period (1 June–31 August 2013) and where a different food vehicle was responsible for illnesses.

METHODS

Ethical approval

The Center for Global Health within the CDC determined that these investigations were in response to a public health threat and did not meet the definition of human subject research, and were therefore exempt from institutional review board approval. In the case-control study conducted, the purpose of the investigation and voluntary nature of participation were explained to all participants and verbal assent was obtained prior to all interviews.

Definitions

We defined a confirmed case as laboratory-confirmed cyclosporiasis in a person who had onset of illness between 1 June and 31 August, and who did not have a history of international travel during the 14 days before symptom onset. We defined a cluster as more than one unrelated ill person (i.e. people who did not know or live with each other), at least one of whom had a laboratory-confirmed infection, who reported eating at the same restaurant, shopping at the same grocery store, or attending the same event (e.g. social gathering) as a confirmed case-patient in the 2–14 days before becoming ill (the incubation period for Cyclospora). Within a cluster, we defined a probable case as diarrhoea (i.e. ⩾3 loose stools in 24 h) in a person who ate food from the same restaurant, grocery store, or event as a confirmed case-patient during the 2- to 14-day incubation period. We further classified a probable case as epidemiologically linked if diarrhoea occurred in a person who ate food with (i.e. dined together in the same group) a confirmed case-patient from the same restaurant within the incubation period.

Outbreak identification and case ascertainment

The investigators used a hypothesis-generating questionnaire to identify potential vehicles of infection and clusters of cases for further investigation. The Texas Department of State Health Services targeted clusters with ⩾3 case-patients and available epidemiological (e.g. onset and exposure dates) and traceback information (e.g. receipts and shopper card information). One cluster was identified at a Mexican-style restaurant in southeastern Texas (restaurant A). A menu-specific questionnaire was used to identify common food items consumed by case-patients who ate at restaurant A. The questionnaire addressed meal date and time and details about menu items consumed by each patron, including condiments. Case-patients were asked to provide names and telephone numbers of their meal companions, which facilitated identification of epidemiologically linked cases and controls.

Two clusters associated with Mexican-style restaurants (restaurants B and C) in central Texas were also identified; neither restaurant was affiliated with restaurant A or each other. An additional cluster of case-patients from a grocery store in northeastern Texas was also identified. Data from shopper cards were used to identify common produce items purchased.

Restaurant A case-control study and environmental investigation

To identify the most likely vehicle(s) of infection for the restaurant A cluster, we conducted a case-control study. We defined a control as a person who ate food from the restaurant and reported no diarrhoea during the 14 days thereafter. We identified controls through credit card receipts, which included patron names and meal dates, and through interviews of case-patients, who provided names and contact information for meal companions. We attempted to identify at least three meal date-matched controls per case-patient. Trained personnel conducted telephone interviews using the menu-specific questionnaire.

The environmental investigation included reviewing with management the daily operation of the restaurant, ordering practices and suppliers for the exposure period, and inspecting and evaluating food storage and preparation areas and practices. We interviewed food handlers to assess what meals they ate at the restaurant and if they had been ill. The chef provided an ingredient list for each menu item and recipes for condiments including salsas.

Traceback investigations

Traceback investigations were conducted to determine common suppliers of produce to the pertinent points of service indicated by the epidemiological investigations. State and local health departments in Texas and CDC contacted the points of service to collect supplier and distributor information, which was forwarded to FDA. FDA district offices contacted the distributors and collected invoices and other records. FDA reviewed records pertaining to purchases made at each level of the distribution chains.

Statistical analysis

For the restaurant A cluster, data were analysed using SAS v. 9.3 (SAS Institute Inc., USA). To identify associations between cyclosporiasis and meal and condiment ingredients, we conducted unmatched and matched analyses of data from case-patients and controls. For many exposures, the number of persons was too small to use asymptotic methods; therefore, we used an exact method (i.e. exact conditional logistic regression) [Reference Mehta, Patel and Senchaudhuri8]. Matched case-control sets were treated as strata in these analyses, allowing us to control for the heterogeneity of risk across matched sets. We report the results as odds ratios (ORs) with corresponding 95% confidence intervals (CIs); we provide a median unbiased estimate of the OR if the upper bound of the CI is infinity.

Laboratory analysis of stool specimens

Stool specimens positive for Cyclospora on examination at the Texas State Public Health Laboratory were sent to CDC's Parasitic Diseases Reference Diagnostic Laboratory for confirmatory testing and identification of the parasite to the species level (i.e. C. cayetanensis). CDC examined wet mounts of the specimens by ultraviolet (UV) fluorescence microscopy to identify Cyclospora oocysts, which are autofluorescent. Because these specimens had been stored in zinc polyvinyl alcohol, they were suitable for molecular analysis. CDC conducted DNA extraction as described previously [Reference da Silva9] and adapted a TaqMan real-time PCR method for species-level identification [Reference Verweij10]. To ensure the validity of the PCR results, CDC examined a subset of the specimens by DNA sequencing of the 18S rRNA gene as described previously [Reference Ho11].

RESULTS

Case reporting for multistate outbreaks

CDC was notified of 631 laboratory-confirmed cases of cyclosporiasis in residents of 25 states whose illness onset dates were during June–August 2013 (Fig. 1). Case-patients had a median age of 52 years (range <1–94 years); 298 (58% of 518) were female. Of the 596 persons with available information, 49 (8%) were hospitalized and no deaths were reported. The three states with the highest numbers of reported cases were Texas (270 cases, 43%), Iowa (140, 22%), and Nebraska (87, 14%). In Iowa and Nebraska, the number of cases peaked in mid-June, whereas in Texas the peak occurred in early July (Fig. 1).

Fig. 1. Confirmed cyclosporiasis cases (n = 631) reported during the investigation period (1 June to 31 August 2013) by week of illness onset. Total cases in the United States are shown in the green bar graph, Texas cases by the red line, and a combination of Iowa and Nebraska cases by the blue line.

More than 70 clusters of cases linked to multiple restaurants and grocery stores in various regions of Texas were identified. Most (86%) of the clusters involved two or three ill persons. Of the 26 clusters (12 restaurants, 14 grocery stores) with ⩾3 ill persons, only four clusters had adequate epidemiological and traceback information to conduct a thorough investigation. The four clusters investigated are summarized in Table 1 and are described below.

Table 1. Summary of investigations of cluster-associated cases of cyclosporiasis in Texas

Restaurant A case-control study

A total of 25 case-patients were enrolled in the case-control study. Of these, 18 were confirmed cases and seven were probable cases, three of which were epidemiologically linked. The four probable cases that were not epidemiologically linked were identified through credit card receipts.

Meal dates were identified for 21 (84%) case-patients and included five dates (Table 2); the telephone interviews were conducted 4–6 weeks after the reported meal dates. The dates of illness onset were known for 22 (88%) case-patients and ranged from 10 July to 24 July (Table 2). The median incubation period was 7 days (n = 18) for both the confirmed (range 4–16 days) and probable (range 6–8 days) cases. We matched by meal date the 21 case-patients whose meal date was known with 65 controls (Table 2).

Table 2. Restaurant A case-control study of cyclosporiasis – number of cases and controls by meal date*

* Restaurant A was closed on Mondays and was closed from 1–4 July for the Independence Day Holiday.

Of 58 ingredients used in preparing food items on the restaurant's menu, ten were significantly associated with cyclosporiasis (Table 3). The only ingredient eaten by all 25 case-patients was cilantro, the ingredient most strongly associated with illness (OR 19·9, 95% CI 4·1–∞). Consumption of lettuce was not associated with illness (iceberg lettuce: matched OR 2·5, 95% CI 0·79–8·4; romaine lettuce: matched OR 3·0, 95% CI 0·16–∞). Neither red cabbage nor carrots (the other components of the salad mix linked to cases of cyclosporiasis in Iowa and Nebraska) were used at restaurant A.

Table 3. Frequencies and odds ratios for selected food exposures in case-control study of cyclosporiasis linked to restaurant A

OR, Odds ratio; CI, confidence interval.

* Not statistically significant in unmatched analysis, but was significant in matched analysis

Restaurant A prepared and served three salsas: side salsa, fire-roasted salsa, and salsa ranchera, as well as one in-house-prepared hot sauce, all of which contained both cilantro and tomatoes. Of these, the side salsa, the fire-roasted salsa, and the hot sauce contained fresh cilantro and were associated with illness (Table 3). The salsa ranchera, which contained only cooked ingredients, was not associated with illness (Table 3). Of note, the side salsa and hot sauce contained canned tomatoes, whereas the fire-roasted salsa contained fresh tomatoes.

The environmental investigation at restaurant A did not identify practices that could result in contamination of the ingredients with Cyclospora. All of the interviewed restaurant staff reported eating at the restaurant, but none reported diarrhoeal illnesses during June and July. No food items from the exposure period were available for laboratory testing.

Two other restaurant clusters

Formal epidemiological studies were not conducted at restaurants B and C because of the small number of cases, three and six, respectively. However, information gathered on the hypothesis-generating questionnaire revealed that all nine case-patients had eaten cilantro in the 14 days prior to symptom onset. Invoices from the two establishments allowed for traceback investigations to be conducted.

Grocery store cluster

Four additional case-patients independently reported having eaten fresh cilantro they purchased at the same local grocery store before they became ill. Shopper card information was available for three of these persons, all three of whom purchased fresh cilantro within a 4-day period (22–25 June) and developed diarrhoeal illness 5–10 days after their purchase. Cilantro was the only common produce item that all three persons purchased at this grocery store.

Traceback investigations and control measures

Available traceback information indicated that restaurant A received cilantro from a produce supplier located in Puebla, Mexico during the period of interest. Restaurants B and C and the grocery store were supplied by the same distribution centre. This distribution centre received cilantro from two suppliers located in Puebla, Mexico, different than the supplier to restaurant A. Thus, Puebla was a shared source of fresh cilantro served at all three restaurants and available at the grocery store during the period when case-patients purchased cilantro. Whether the cilantro came from the same location in Puebla or was processed at the same facility could not be determined. As a result of this investigation, FDA increased its surveillance efforts on cilantro products exported to the United States from Mexico [7].

Laboratory analysis of stool specimens

CDC confirmed the presence of Cyclospora oocysts and C. cayetanensis DNA by UV fluorescence microscopy and real-time PCR analysis, respectively, in all 66 specimens received from case-patients in Texas. DNA sequencing, which was performed for ten of these specimens, confirmed the PCR results.

DISCUSSION

The summer 2013 outbreaks represent one of the largest numbers of reported cyclosporiasis cases in the United States since it was added to the list of nationally notifiable diseases in 1999; and contributed to the highest annual number of cyclosporiasis cases since 1997. The highest number of reported outbreak-associated cases of cyclosporiasis since it became nationally notifiable was 692, which occurred in 2005 [12]. Since then, between 2006 and 2011, the median annual number of reported cases of cyclosporiasis has been 140 (range 93–179) [Reference Adams13], which typically includes travel-associated and outbreak cases. Between 2000 and 2011 there was a median of 21 cases (range 9–151) of cyclosporiasis reported in the United States from June to August.

Cilantro was the most likely vehicle of infection in restaurant A, B, C, and grocery store clusters. The strong positive association between cilantro consumption and illness and the data from ingredient-level analyses of the salsa in the case-control study, along with the consistency of cilantro exposure among the case-patients in all four investigated clusters, provide compelling evidence of cilantro as the vehicle of infection. Although a thorough investigation could not be conducted on the remaining clusters in Texas, the temporal association of these four clusters with the large overall increase in cyclosporiasis cases in Texas suggests cilantro was the vehicle of infection for many other cases in Texas.

In Table 3, the ORs for corn tortilla, garlic, and salt are high; this is due to the effect of confounding. These three items are confounded with cilantro probably because they all measure the same latent variable – whether or not a person ate chips and side salsa. All patrons of restaurant A were served chips, made with corn tortillas, and side salsa upon arrival at the table. Notably, garlic and salt were ingredients used in the preparation of most of the menu items served in restaurant A. Moreover, these three items are not biologically plausible vehicles of infection for Cyclospora. Historically, foodborne outbreaks of cyclosporiasis have been associated with fresh produce that does not have an outer shell that needs to be removed prior to consumption.

Restaurant-associated illnesses in Iowa and Nebraska during June 2013 were linked to a prepackaged salad mix from a supplier in Guanajuato [14], whereas the fresh cilantro linked to the Texas clusters was grown in Puebla [7]. Therefore, there were at least two US outbreaks of cyclosporiasis associated with different food vehicles from different regions of Mexico during summer 2013.

The occurrence of multiple outbreaks of foodborne cyclosporiasis linked to different types of fresh produce during a single season is not unprecedented. During March to July 1997, three separate and unrelated US outbreaks of cyclosporiasis occurred, which were linked to mesclun lettuce from Peru, raspberries from Guatemala, and basil from multiple possible sources [Reference Herwaldt1].

During 2011 and 2012, CDC assisted with two additional investigations in which cilantro was a likely vehicle of infection for C. cayetanensis. In 2011, the Florida Department of Health investigated a restaurant-associated outbreak of 12 cases of cyclosporiasis [15]. Epidemiological and environmental investigations suggested cilantro and onions as the most likely vehicles of infection, because these two ingredients were used in all meals eaten by case-patients. Unfortunately, traceback investigations could not be performed because invoices and receipts were not available [15]. In 2012, state and local health departments in Texas investigated cases of cyclosporiasis associated with a Mexican-style restaurant. A case-control study of 16 cases and 12 controls suggested that fish tacos, containing cabbage and cilantro, were linked to infection. However, a vehicle was not conclusively identified and traceback investigations could not be completed. Most recently, in 2014, investigations conducted of Mexican-style restaurant clusters in Texas linked illnesses again to cilantro imported from Puebla, Mexico [16, 17].

Investigations of foodborne outbreaks in general and cyclosporiasis specifically pose many challenges. In general, patients may not recall the pertinent food exposure that occurred weeks to months before they are interviewed, and typically the food items are no longer available for testing once an investigation is under way [Reference Herwaldt1, Reference Shah18]. Additionally, many fresh produce items are served as garnishes, incorporated into a mixture with other plausible ingredients (e.g. salad mix and fruit salad), or used in other ways that are inconspicuous. Specific to cyclosporiasis is the relatively long incubation period compounded by delays in diagnosis and reporting of cases that may impede the recognition of an outbreak. Moreover, in most laboratories, routine stool analysis for ova and parasites may not include the examination for the presence of Cyclospora oocysts; such testing must be specifically requested, leading to delays in diagnosis. In our experience UV fluorescence microscopy of unstained wet mounts is sensitive and significantly less time-consuming and labour-intensive. However, molecular methods are required to characterize the parasite to the species level.

Determining whether cases of cyclosporiasis are linked to each other and to particular food items is a major challenge. For example, we could not determine the vehicle of infection for the majority of cases in the Texas investigation; the paucity of data to link these cases precluded formal epidemiological investigations. The outbreaks of cyclosporiasis in 2013 underscore the need for molecular subtyping to complement evidence from epidemiological investigations, potentially assisting in identifying the number of outbreaks in a given season and suggesting links between clusters, and facilitating source tracking. Molecular methods that can differentiate C. cayetanensis to the haplotype or genotype level have yet to be developed [Reference Sulaiman19]. This research is limited by the difficulty in obtaining C. cayetanensis oocysts/DNA for analysis, further compounded by the need to obtain and analyse specimens from geographically diverse settings. Of note, infected humans are the only known source of the parasite, and no methods to reproduce these oocysts in vitro or in vivo have been established [Reference Herwaldt1]. If candidate subtyping markers are identified in the future, retrospective analysis of stool specimens, such as those that CDC tested by molecular methods in 2013, could be useful in the validation process of potential genotyping methods.

An increasing number of foodborne outbreaks have been associated with the consumption of fresh produce [Reference Barton20Reference McCollum22]. Reducing foodborne illness linked to produce consumption continues to be a difficult task for public health and the produce industry. The specific challenges posed by Cyclospora include under-detection of cases, lack of subtyping methods to link cases to each other or to specific food items, and the absence of practical tools to detect the organism in food and potential sources of contamination in the environment (e.g. soil and insanitary irrigation water). Advances in these areas may assist in better understanding the biology of C. cayetanensis, the epidemiology of cyclosporiasis, and aid in establishing control measures to reduce contamination of fresh produce.

APPENDIX

Cyclosporiasis Outbreak Investigation Team

C. B. Behravesh, T. Benedict, C. Braden, M. de Almeida, J. Jones, A. Kerk, C. Kiebler, B. Mathison, S. Montgomery, C. Schwensohn (Centers for Disease Control and Prevention, Atlanta, GA); T. Baker, C. Davis, N. Drake, G. Gana, C. Lozano, K. Klein, D. Olinger, K. Reynolds, A. Ryder (Fort Bend County Health & Human Services, Rosenberg, TX); T. Lee (City of Rosenberg Health Department, Rosenberg, TX).

ACKNOWLEDGEMENTS

The authors sincerely thank the owner and chef of restaurant A for their cooperation, openness, and willingness to assist with the case-control investigation. We also thank all the restaurant and grocery store owners and the participants for the information provided to assist with all the investigations.

This work was supported by the Centers for Disease Control and Prevention, Center for Global Health, Division of Parasitic Diseases and Malaria, and the National Center for Emerging and Zoonotic Infectious Diseases, Division of Foodborne, Waterborne & Environmental Diseases.

The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

DECLARATION OF INTEREST

None.

References

REFERENCES

1. Herwaldt, BL. Cyclospora cayetanensis: a review, focusing on the outbreaks of cyclosporiasis in the 1990s. Clinical Infectious Diseases 2000; 31: 10401057.Google Scholar
2. Hall, RL, Jones, JL, Herwaldt, BL. Surveillance for laboratory-confirmed sporadic cases of cyclosporiasis – United States, 1997–2008. Morbidity and Mortality Weekly Report. Surveillance Summaries 2011; 60: 1–11.Google Scholar
3. Centers for Disease Control and Prevention. Outbreak of cyclosporiasis associated with snow peas – Pennsylvania, 2004. Morbidity and Mortality Weekly Report 2004; 53: 876–878.Google Scholar
4. Herwaldt, BL, Ackers, ML. An outbreak in 1996 of cyclosporiasis associated with imported raspberries. The Cyclospora Working Group. New England Jour- nal of Medicine 1997; 336: 15481556.Google Scholar
5. Ortega, YR, et al. Cyclospora species – a new protozoan pathogen of humans. New England Journal of Medicine 1993; 328: 13081312.Google Scholar
6. Centers for Disease Control and Prevention. National Notifiable Diseases Surveillance System (NNDSS) (http://wwwn.cdc.gov/nndss/). Accessed 8 January 2014.Google Scholar
7. U.S. Food and Drug Administration. FDA investigates multistate outbreak of cyclosporiasis (http://www.fda.gov/Food/RecallsOutbreaksEmergencies/Outbreaks/ucm361637.htm#updates). Accessed 26 February 2014.Google Scholar
8. Mehta, CR, Patel, N, Senchaudhuri, P. Exact stratified linear rank tests for ordered categorical and binary data. Journal of Computational and Graphical Statistics 1992; 1: 2140.Google Scholar
9. da Silva, AJ, et al. Fast and reliable extraction of protozoan parasite DNA from fecal specimens. Molecular Diagnosis 1999; 4: 5764.Google Scholar
10. Verweij, JJ, et al. Detection of Cyclospora cayetanensis in travellers returning from the tropics and subtropics using microscopy and real-time PCR. International Journal of Medical Microbiology 2003; 293: 199202.Google Scholar
11. Ho, AY, et al. Outbreak of cyclosporiasis associated with imported raspberries, Philadelphia, Pennsylvania, 2000. Emerging Infectious Diseases 2002; 8: 783788.Google Scholar
12. Centers for Disease Control and Prevention. U.S. foodborne outbreaks of cyclosporiasis - 2000-2013 (http://www.cdc.gov/parasites/cyclosporiasis/outbreaks/foodborneoutbreaks.html). Accessed 27 February 2015.Google Scholar
13. Adams, DA, et al. Summary of notifiable diseases – United States, 2011. Morbidity and Mortality Weekly Report 2013; 60: 1–117.Google Scholar
14. U.S. Food and Drug Administration. Environmental assessment: 2013 cyclosporiasis outbreak in Iowa and Nebraska – findings and recommendations (http://www.fda.gov/Food/RecallsOutbreaksEmergencies/Outbreaks/ucm375732.htm). Accessed 8 January 2014.Google Scholar
16. Centers for Disease Control and Prevention. Cyclosporiasis outbreak investigations - United States, 2014 (http://www.cdc.gov/parasites/cyclosporiasis/outbreaks/2014/). Accessed 26 February 2015.Google Scholar
17. U.S. Food and Drug Administration. FDA investigates outbreak of cyclosporiasis (http://www.fda.gov/food/recallsoutbreaksemergencies/outbreaks/ucm411990.htm). Accessed 26 February 2015.Google Scholar
18. Shah, L, et al. Challenges of investigating community outbreaks of cyclosporiasis, British Columbia, Canada. Emerging Infectious Diseases 2009; 15: 12861288.Google Scholar
19. Sulaiman, IM, et al. Genetic characterization of human-pathogenic Cyclospora cayetanensis parasites from three endemic regions at the 18S ribosomal RNA locus. Infection, Genetics and Evolution 2014; 22: 229234.Google Scholar
20. Barton, Behravesh C, et al. 2008 outbreak of Salmonella Saintpaul infections associated with raw produce. New England Journal of Medicine 2011; 364: 918927.Google Scholar
21. Kozak, GK, et al. Foodborne outbreaks in Canada linked to produce: 2001 through 2009. Journal of Food Protection 2013; 76: 173183.CrossRefGoogle ScholarPubMed
22. McCollum, JT, et al. Multistate outbreak of listeriosis associated with cantaloupe. New England Journal of Medicine 2013; 369: 944953.Google Scholar
Figure 0

Fig. 1. Confirmed cyclosporiasis cases (n = 631) reported during the investigation period (1 June to 31 August 2013) by week of illness onset. Total cases in the United States are shown in the green bar graph, Texas cases by the red line, and a combination of Iowa and Nebraska cases by the blue line.

Figure 1

Table 1. Summary of investigations of cluster-associated cases of cyclosporiasis in Texas

Figure 2

Table 2. Restaurant A case-control study of cyclosporiasis – number of cases and controls by meal date*

Figure 3

Table 3. Frequencies and odds ratios for selected food exposures in case-control study of cyclosporiasis linked to restaurant A